VACCINE FORMULATIONS
Background of the Invention
[0001] Pneumococcal disease caused by the bacterium Streptococcus
pneumoniae (also known as pneumococcus) is one of the more important bacterial
pathogens across globe. The disease burden is high in the developing countries in
children under five years of age where the vaccine is not available. Pneumococcal
disease is a complex group of illnesses and includes invasive infections such as
bacteremia/sepsis, meningitis, pneumonia and otitis media, which affects both
children and adults. Prevnar 13 (also known as "Prevenar 13" and referred to
herein as "Prev(e)nar 13") is a formulation of polysaccharides from thirteen
pneumococcal serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F))
which are individually conjugated to CRM 197 (Cross Reactive Material from a
mutant strain of Corynebacterim diphtheriae). Prev(e)nar 13 is recommended for
active immunization of infants and toddlers to provide the broadest serotype
coverage of any pneumococcal conjugate vaccines. Notably, serotype 19A in
Prev(e)nar 13 is prevalent in many regions of the world and is often associated
with antibiotic resistance. See e.g., WO2006/1 10381; WO2008/079653;
WO2008/079732; WO2008/143709 and references cited therein.
[0002] Thimerosal (also known as Thiomersal; merthiolate) is an ethylmercurycontaining
preservative which has, since the early 1930s, been added to many
multi-dose injectable formulations and topical solutions to protect them from
potential contamination during exposure and when administered to multiple
subjects. Thimerosal continues to be administered, as part of mandated
immunizations and in other pharmaceutical products in the United States and the
rest of the world. It is claimed to be an effective preservative for eliminating
potential contaminating bacteria during multiple use of products in the field, with
minimum interaction with the antigenic structure and properties of vaccines. Due
to mounting controversies regarding potential safety issues and adverse effects of
ethylmercury on brain development in infants and youth, certain agencies began
recommending that alternative preservatives with a lower or negligible safety risk
be identified. In 1999, a U.S. Food and Drug Administration review mandated by
the U.S. Congress found that some infants might receive more mercury from
vaccines than was considered acceptable according to certain national guidelines.
The American Academy of Pediatrics (AAP) and US Public Health Service
(USPHS) issued a joint statement concerning Thimerosal in vaccines and then the
AAP released an interim report to clinicians recommending removal of Thimerosal
from vaccines as soon as possible, while maintaining efforts to ensure high levels
of vaccination continue to be implemented worldwide without affecting safety.
[0003] The need for adding preservatives to vaccines can be reduced or obviated
by making and using only single-dose vaccine formulations. However, use of
single-dose preservative-free formulations raises the overall cost of vaccination
and jeopardizes the effectiveness of immunization programs in developing
countries. In addition, removing preservatives from multi-dose vials altogether is
not viewed as a preferred option, especially in countries with limited cold storage
and suboptimal standards of health care (Drain et al., Bull World Health Organ
81(10): 726 - 731 (2003). In 1928, twelve out of 2 1 children inoculated with
contaminated diphtheria vaccine died of multiple staphylococcal abscesses and
toxemia (Wilson, The Hazards of Immunization , Athlone Press, London pp. 75 -
78 (1967). Thus, although multi-dose vials appear to be most appropriate for the
production of less expensive vaccines, it is desirable to formulate multi-dose
vaccines with at least one preservative to protect subjects from micro-organisms
inadvertently introduced into the vaccine during multiple uses or after one or more
non-sterile events. The efficacy of preservatives in resisting bacterial and other
micro-organism contaminations must be balanced, however, with the effect that a
particular preservative has on the immunogenicity as well as on the long term
stability of each different antigenic determinant in an immunogenic composition of
choice. The compatibility of Prev(e)nar 13 formulations with preservatives has not
been previously addressed. It would be desirable to have an optimized formulation
comprising at least one preservative that protects and/or stabilizes antigenic
determinants of the pneumococcal antigen serotypes present in Prev(e)nar 13.
Summary of the Invention
[0004] In a first aspect, the present invention provides a multivalent
immunogenic composition comprising a plurality of capsular polysaccharides from
Streptococcus pneumoniae serotypes and 2-phenoxyethanol (2-PE). In certain
embodiments, the capsular polysaccharides are from one or more of the
Streptococcus pneumoniae serotypes selected from 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14,
18C, 19A, 19F and 23F. In certain embodiments, capsular polysaccharides are
from seven or more of the Streptococcus pneumoniae serotypes selected from 1, 3,
4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F. In certain embodiments,
capsular polysaccharides are from each of the Streptococcuspneumoniae serotypes
1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F.
[0005] In certain embodiments of the invention, the composition comprises 2-PE
at a concentration of between 7 mg/mL and 15 mg/mL, about 10 mg/mL, not less
than 7mg/mL, not less than lOmg/mL, or not less than 15mg/mL.
[0006] Immunogenic compositions of the invention may, in certain
embodiments, further comprises one or more of an adjuvant, a buffer, a
cryoprotectant, a salt, a divalent cation, a non-ionic detergent, and an inhibitor of
free radical oxidation. In certain embodiments, the adjuvant is aluminum
phosphate.
[0007] A preferred multivalent immunogenic composition of the invention is a
formulation of pneumococcal capsular polysaccharides from serotypes 1, 3, 4, 5,
6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F, individually conjugated to CRMi 7,
wherein the multivalent immunogenic composition is formulated in a sterile liquid
to comprise: about 4.4 mg/mL of each polysaccharide, except for 6B at about 8.8
mg/mL; about 58 mg/mL CRMi carrier protein; about 0.25 mg/mL of elemental
aluminum in the form of aluminum phosphate; about 0.85% sodium chloride;
about 0.02% polysorbate 80; about 5 mM sodium succinate buffer at a pH of 5.8;
and about 10 mg/mL of 2-phenoxyethanol.
[0008] In certain embodiments of the invention, the antigenicity of the
immunogenic composition is stable for not less than 1 year, 1.5 years, 2 years or
2.5 years at a temperature of 2-8°C, 20-25°C, or 37°C.
[0009] In certain embodiments of the invention, following the inoculation of the
immunogenic composition with one or more micro-organisms, the concentration of
said micro-organisms is reduced over time. In certain embodiments, following
inoculation with one or more bacteria strains, the composition presents at least 1.0
log reduction from the initial micro-organism count at 24 hours, at least 3.0 log
reduction at 7 days from the previous value measured and not more than 0.5 log
increase after 28 days, from the previous value measured. In certain embodiments,
following inoculation with one or more bacteria strains, the composition presents
at least 2.0 log reduction from the initial calculated count at 6 hours after
inoculation, at least 3.0 log reduction from the previous value measured at 24 hours
and no recovery at 28 days. Micro-organism strains include one or more strains
selected from P. aeruginosa, S. aureus, E. coli and B. subtilis.
[0010] In certain embodiments, the immunogenic composition is inoculated
multiple times. In certain embodiments, a second inoculation occurs at 6 hours
following the initial inoculation, a third inoculation occurs at 24 hours following
the initial inoculation, a third inoculation occurs as 7 days following the initial
inoculation and a fourth inoculation occurs at 14 days following the initial
inoculation.
[0011] In a second aspect, the present invention also provides a vial containing a
multivalent immunogenic composition of the invention. A vial may contain a
single dose or more than one dose of the immunogenic composition. The
invention also provides a pre-filled vaccine delivery device comprising a
multivalent immunogenic composition of the invention. In certain embodiments,
the pre-filled vaccine delivery device is or comprises a syringe. Vaccine delivery
devices of the invention may comprise a dual or multiple chamber syringe or vials
or combinations thereof. In certain embodiments, the pre-filled vaccine delivery
device comprises a multivalent immunogenic composition formulated for
intramuscular or subcutaneous injection.
[0012] In a third aspect, the present invention also provides a kit for preparing a
multivalent immunogenic composition of the invention, wherein the kit comprises
(i) a plurality of capsular polysaccharides in a lyophilized form of the composition,
and (ii) aqueous material for reconstituting component (i) in order to provide the
aqueous composition.
[0013] In a fourth aspect, the present invention provides a multi-dose vaccine
comprising four doses of a vaccine in a vial, each dose comprising from 4 to 20
mg/mL, preferably 10 mg/mL of 2-phenoxyethanol, wherein a dose is 0.5 mL of
vaccine.
[0014] In a fifth aspect, the present invention also provide a method for
measuring the efficacy of a vaccine formulation comprising one or more select
preservative agents in the presence of some or all of the immunogenic and nonimmunogenic
components of the vaccine composition, wherein the test comprises
at least two steps of inoculating the test composition with a select micro-organism
population and comparing the log reduction of inoculated micro -organism(s) over
time and under particular environmental conditions (e.g., temperature) to the log
reduction in a control composition lacking the test preservative(s).
Brief Description of the Drawings
[0015] Figure 1 - Effectiveness of Thimerosal as a vaccine preservative in
various formulations.
[0016] Figure 2 - Effectiveness and stability of 2-phenoxyehtanol (2-PE) as a
vaccine preservative in various formulations and at various concentrations.
[0017] Figure 3 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with no preservative at 20-25°C after a single
challenge of micro-organisms (expressed as mean logio change compared to time
of challenge at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0018] Figure 4 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with 0.01% Thimerosal at 20-25°C after a
single challenge of micro-organisms (expressed as mean logio change compared to
time of challenge at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0019] Figure 5 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with 0.02% Thimerosal at 20-25°C after a
single challenge of micro-organisms (expressed as mean logio change compared to
time of challenge at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0020] Figure 6 - Time course of micro-organism colony count reduction in
saline with 0.02% Thimerosal at 20-25°C after a single challenge of micro
organisms (expressed as mean logio change compared to time of challenge at t=0, 6
hours, 24 hours, 7 days, 14 days and 28 days).
[0021] Figure 7 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with 5 mg/0.5 mL 2-phenoxyethanol at 20-25°C
after a single challenge of micro-organisms (expressed as mean logio change
compared to time of challenge at t=0, 6 hours, 24 hours, 7 days, 14 days and 28
days).
[0022] Figure 8 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with no preservative at (A) 22 - 24°C or at (B)
2 - 8°C, after multiple challenges of micro-organisms at t=0, 6 hours, 24 hours, 7
days and 14 days (expressed as mean logio change compared to time of challenge
at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0023] Figure 9 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with 0.01% Thimerosal at (A) 22 - 24°C or at
(B) 2 - 8°C, after multiple challenges of micro-organisms at t=0, 6 hours, 24 hours,
7 days and 14 days, (expressed as mean log io change compared to time of
challenge at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0024] Figure 10 - Time course of micro-organism colony count reduction in
Prev(e)nar 13 vaccine formulation with 0.02% Thimerosal at (A) 22 - 24°C or at
(B) 2 - 8°C after multiple challenges of micro-organisms at t=0, 6 hours, 24 hours,
7 days and 14 days (expressed as mean logio change compared to time of challenge
at t=0, 6 hours, 24 hours, 7 days, 14 days and 28 days).
[0025] Figure 11 - Time course of micro-organism colony count reduction in
saline with 0.02% Thimerosal at (A) 22 - 24 °C or at (B) 2 - 8°C after multiple
challenges of micro-organisms at t=0, 6 hours, 24 hours, 7 days and 14 days
(expressed as mean logio change compared to time of challenge at t=0, 6 hours, 24
hours, 7 days, 14 days and 28 days).
[0026] Figure 12 - Non-linear regression analysis of S. aureus decay in various
challenge studies.
[0027] Figure 13 - Comparison of 2-PE and Thimerosal as a vaccine
preservative against single or multiple challenges of micro-organisms: Passing or
failing EP 5.1.3 criteria B.
[0028] Figure 14 - Long term stability of antigenicity of Streptococcus
pneumoniae polysaccharide preparations from each serotype in Prev(e)nar 13
formulated with 5 mg 2-PE.
[0029] Figure 15 - Long term stability of 2-PE in Prev(e)nar 13 vaccine
formulation.
Detailed Description of the Invention
[0030] Percentage concentration, as used in this application, is weight to volume
(w/v) or weight to weight (w/w).
[0031] Unless specified otherwise, "dose" refers to a vaccine dose of 0.5 mL.
[0032] The term "multi-dose" refers to a composition which comprises more than
one dose of vaccine, which may be administered to one subject or more than one
subject in different administration steps and over time.
[0033] The present invention provides a multivalent immunogenic composition
comprising a plurality of capsular polysaccharides from Streptococcuspneumoniae
(also known as pneumococcus) serotypes and a preservative. This composition
may be also be referred to as a vaccine and be used to induce an immune response
against pneumococcus and to protect against infection in a subject, e.g., a human
subject, preferably a human child or infant.
[0034] A plurality of any Streptococcus pneumoniae capsular polysaccharides is
suitable for the composition of the present invention. In certain embodiments of
the invention, the multivalent immunogenic composition comprises capsular
polysaccharides prepared from serotypes 4, 6B, 9V, 14, 18C, 19F and 23F of
Streptococcus pneumoniae. In certain embodiments, the capsular polysaccharides
are prepared from serotypes 4, 6B, 9V, 14, 18C, 19F, 23F and at least one
additional serotype of Streptococcus pneumoniae. In certain embodiments, the
capsular polysaccharides are prepared from at least 4, at least 5, at least 6, at least
7, at least 8, or at least 9 serotypes selected from serotypes 1, 4, 5, 6B, 7F, 9V, 14,
18C, 19F and 23F of Streptococcus pneumoniae. In certain embodiments, the
capsular polysaccharides are prepared from serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V,
14, 18C, 19A, 19F and 23F of Streptococcus pneumoniae. Capsular
polysaccharides of the invention are prepared from serotypes of Streptococcus
pneumoniae using known techniques. See, e.g., International Patent Applications
WO2006/1 10381; WO2008/079653; WO2008/079732 and WO2008/143709, each
of which is incorporated herein by reference.
[0035] In certain embodiments of the invention, the capsular polysaccharides are
conjugated to a carrier protein. These pneumococcal conjugates may be prepared
separately. For example, in one embodiment, each pneumococcal polysaccharide
serotype is grown in a soy-based medium. The individual polysaccharides are then
purified through centrifugation, precipitation, ultra-filtration and column
chromatography. The purified polysaccharides are chemically activated so that the
saccharides are capable of reacting with the selected carrier protein to form
pneumococcal conjugates.
[0036] Once activated, each capsular polysaccharide is separately conjugated to a
carrier protein to form a glycoconjugate. In certain embodiments, each different
capsular polysaccharide is conjugated to the same carrier protein. In such
embodiments, conjugation may be accomplished by, e.g., reductive amination.
[0037] The chemical activation of the polysaccharides and subsequent
conjugation to the carrier protein are achieved by conventional means. See, for
example, U.S. Patent Nos. 4,673,574 and 4,902,506, incorporated herein by
reference.
[0038] Carrier proteins are preferably proteins that are non-toxic and nonreactogenic
and obtainable in sufficient amount and purity. Carrier proteins should
be amenable to standard conjugation procedures. In certain embodiments of the
present invention, CRM197 is used as the carrier protein.
[0039] CRM 197 (Pfizer, Sanford, NC) is a non-toxic variant (i.e., toxoid) of
diphtheria toxin isolated from cultures of Corynebacterium diphtheria strain C7
(CRM 197) grown in casamino acids and yeast extract-based medium. CRM 197 is
purified through ultra-filtration, ammonium sulfate precipitation, and ion-exchange
chromatography. Alternatively, CRM197 is prepared recombinantly in accordance,
e.g., with U.S. Patent No. 5,614,382, which is hereby incorporated by reference.
Other diphtheria toxoids are also suitable for use as carrier proteins.
[0040] Other suitable carrier proteins include inactivated bacterial toxins such as
tetanus toxoid, pertussis toxoid, cholera toxoid (e.g., as described in International
Patent Application WO2004/083251), E. coli LT, E. coli ST, and exotoxin A from
Pseudomonas aeruginosa. Bacterial outer membrane proteins such as outer
membrane complex c (OMPC), porins, transferrin binding proteins, pneumolysin,
pneumococcal surface protein A (PspA), pneumococcal adhesin protein (PsaA),
C5a peptidase from Group A or Group B streptococcus, or Haemophilus influenzae
protein D, can also be used. Other proteins, such as ovalbumin, keyhole limpet
hemocyanin (KLH), bovine serum albumin (BSA) or purified protein derivative of
tuberculin (PPD) can also be used as carrier proteins.
[0041] After conjugation of the capsular polysaccharide to the carrier protein, the
polysaccharide-protein conjugates are purified (i.e., enriched with respect to the
amount of polysaccharide-protein conjugate) by a variety of techniques. These
techniques include concentration/diafiltration operations, precipitation/elution,
column chromatography, and depth filtration.
[0042] As discussed in more detail below, immunogenic compositions of the
present invention comprise at least one preservative useful for producing multidose
vaccine formulations having advantageous properties with respect to long
term stability of one or more antigenic determinants of the multivalent
pneumococcal capsular polysaccharide-protein conjugates and which
advantageously protect the compositions from contamination by conferring
resistance to one or more micro-organisms prior to administration to a subject in
need thereof.
[0043] Additional formulation of the preservative-containing immunogenic
composition of the present invention may be accomplished using art-recognized
methods. For instance, the thirteen individual pneumococcal conjugates may be
formulated with a physiologically acceptable vehicle to prepare the composition.
Examples of such vehicles include, but are not limited to, water, buffered saline,
polyols (e.g., glycerol, propylene glycol, liquid polyethylene glycol) and dextrose
solutions, as described in more detail below.
[0044] The immunogenic compositions of the invention comprise one or more
preservatives in addition to a plurality of pneumococcal capsular polysaccharideprotein
conjugates. The FDA requires that biological products in multiple-dose
(multi-dose) vials contain a preservative, with only a few exceptions. Vaccine
products containing preservatives include vaccines containing benzethonium
chloride (anthrax), 2-phenoxyethanol (DTaP, HepA, Lyme, Polio (parenteral)),
phenol (Pneumo, Typhoid (parenteral), Vaccinia) and thimerosal (DTaP, DT, Td,
HepB, Hib, Influenza, JE, Mening, Pneumo, Rabies). Preservatives approved for
use in injectable drugs include, e.g., chlorobutanol, m-cresol, methylparaben,
propylparaben, 2-phenoxyethanol, benzethonium chloride, benzalkonium chloride,
benzoic acid, benzyl alcohol, phenol, thimerosal and phenylmercuric nitrate.
[0045] Having tested a variety of potentially suitable formulations comprising a
preservative for enhanced effectiveness and stability of Prev(e)nar 13
immunogenic compositions, the invention disclosed herein provides such
pneumococcal immunogenic compositions comprising 2-phenoxyethanol (2-PE) at
a concentration of about 2.5 -10 mg/dose (0.5 - 2%). In certain embodiments, the
concentration of 2-PE is about 3.5 - 7.5 mg/dose (0.7 - 1.5%). In certain
embodiments, the concentration of 2 -PE is about 5 mg/dose (1%). In certain
embodiments, the concentration of 2-PE is not less than 3.5 mg/dose (0.7%>), not
less than 4.0 mg/dose (0.8%>), not less than 4.5 mg/dose (0.9%>), not less than 5.0
mg/dose (1%), not less than 5.5 mg/dose (1.1%), not less than 6.0 mg/dose (1.2%),
not less than 6.5 mg/dose (1.3%), not less than 7.0 mg/dose, not less than 7.5
mg/dose (1.5%), not less than 8.0 mg/dose (1.6%), not less than 9.0 mg/dose
(1.8%) or not less than 10 mg/dose (2%).
[0046] In certain embodiments of the invention, the pneumococcal immunogenic
compositions contain one or more additional preservatives including, but not
limited to, Thimerosal and formalin.
[0047] In certain embodiments, the immunogenic composition may comprise one
or more adjuvants. As defined herein, an "adjuvant" is a substance that serves to
enhance the immunogenicity of an immunogenic composition of this invention.
Thus, adjuvants are often given to boost the immune response and are well known
to the skilled artisan. Suitable adjuvants to enhance effectiveness of the
composition include, but are not limited to:
(1) aluminum salts (alum), such as aluminum hydroxide, aluminum
phosphate, aluminum sulfate, etc.;
(2) oil-in-water emulsion formulations (with or without other specific
immuno-stimulating agents such as muramyl peptides (defined below) or bacterial
cell wall components), such as, for example,
(a) MF59 (PCT Application WO 90/14837), containing 5%
Squalene, 0.5% Tween 80, and 0.5% Span 85 (optionally containing various
amounts of MTP-PE (see below, although not required)) formulated into
submicron particles using a microfluidizer such as Model HOY microfluidizer
(Microfluidics, Newton, MA),
(b) SAF, containing 10% Squalene, 0.4% Tween 80, 5% pluronicblocked
polymer L121, and thr-MDP (see below) either microfluidized into a
submicron emulsion or vortexed to generate a larger particle size emulsion, and
(c) Ribi adjuvant system (RAS), (Corixa, Hamilton, MT) containing
2% Squalene, 0.2% Tween 80, and one or more bacterial cell wall components
from the group consisting of 3-O-deaylated monophosphorylipid A (MPL)
described in U.S. Patent No. 4,912,094 (Corixa), trehalose dimycolate (TDM), and
cell wall skeleton (CWS), preferably MPL + CWS (Detox);
(d) Polysorbate 80 (Tween 80);
(3) saponin adjuvants, such as Quil A or STIMULON QS-21 (Antigenics,
Framingham, MA) (U.S. Patent No. 5,057,540) may be used or particles generated
therefrom such as ISCOMs (immuno-stimulating complexes);
(4) bacterial lipopolysaccharides, synthetic lipid A analogs such as
aminoalkyl glucosamine phosphate compounds (AGP), or derivatives or analogs
thereof, which are available from Corixa, and which are described in U.S. Patent
No. 6,1 13,918; one such AGP is 2-[(R)-3-Tetradecanoyloxytetradecanoylamino]
ethyl 2-Deoxy-4-0-phosphono-3-0-[(R)-3-tetradecanoyloxytetradecanoyl]-2-[(R)-
3-tetradecanoyloxytetradecanoylamino]-b-D-glucopyranoside, which is also know
as 529 (formerly known as RC529), which is formulated as an aqueous form or as
a stable emulsion, synthetic polynucleotides such as oligonucleotides containing
CpG motif(s) (U.S. Patent No. 6,207,646);
(5) cytokines, such as interleukins (e.g., IL-1, IL-2, IL-4, IL-5, IL-6, IL-7,
IL-12, IL-15, IL-18, etc.), interferons (e.g., gamma interferon), granulocyte
macrophage colony stimulating factor (GM-CSF), macrophage colony stimulating
factor (M-CSF), tumor necrosis factor (TNF), costimulatory molecules B7-1 and
B7-2, etc.;
(6) detoxified mutants of a bacterial ADP-ribosylating toxin such as a
cholera toxin (CT) either in a wild-type or mutant form, for example, where the
glutamic acid at amino acid position 29 is replaced by another amino acid,
preferably a histidine, in accordance with published international patent application
number WO 00/18434 (see also WO 02/098368 and WO 02/098369), a pertussis
toxin (PT), or an E. coli heat-labile toxin (LT), particularly LT-K63, LT-R72, CTS109,
PT-K9/G129 (see, e.g., WO 93/13302 and WO 92/19265); and
(7) other substances that act as immuno-stimulating agents to enhance the
effectiveness of the composition, such as calcium salt, iron, zinc, acylated tyrosine
suspension, acylated sugar, derivatized sugars/saccharides, polyphosphazenes,
biodegradable microspheres, monophosphoryl lipid A (MPL), lipid A derivatives
(e.g. of reduced toxicity), 3-O-deacylated MPL, quil A, Saponin, QS21, tocol,
Freund's Incomplete Adjuvant (Difco Laboratories, Detroit, MI), Merck Adjuvant
65 (Merck and Company, Inc., Rahway, NJ), AS-2 (Smith-Kline Beecham,
Philadelphia, PA), CpG oligonucleotides (preferably unmethylated), bioadhesives
and mucoadhesives, microparticles, liposomes, polyoxyethylene ether
formulations, polyoxyethylene ester formulations, and muramyl peptides or
imidazoquinolone compounds. Muramyl peptides include, but are not limited to,
N-acetyl-muramyl-L-threonyl-D-isoglutamine (thr-MDP), N-acetyl-normuramyl-
L-alanine-2-(l'-2' dipalmitoyl-sn-glycero-3-hydroxyphosphoryloxy)-ethylamine
(MTP-PE), and the like.
[0048] In certain embodiments, the adjuvant composition is one which favors
induction of THl-type cytokines (e.g. IFN-g , TNFa, IL-2 and IL-12) to a greater
extent than TH2-type cytokines, which may favor the induction of cell mediated
immune responses to an administered antigen. Particular adjuvant systems which
promote a predominantly THl response include but are not limited to lipid A
derivatives, such as Monophosphoryl lipid A (MPL) or its derivatives, e.g. 3-de-Oacylated
MPL (3D-MPL), a combination of MPL and/or 3D-MPL and an
aluminum salt and/or a saponin derivative (e.g., QS21 in combination with 3DMPL
as disclosed in WO 94/00153, or QS21 and cholesterol as disclosed in WO
96/33739), triterpenoids, and oil-in-water emulsions such as one comprising
tocopherol (as disclosed in WO 95/17210).
[0049] An adjuvant may optionally be adsorbed by or combined with one or
more of the immunogenic components of the preserved vaccine formulation of the
invention. As used herein, the term "adsorbed antigen" refers to a mixture in
which greater than 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of an antigen is
adsorbed to adjuvant. In certain embodiments, the adjuvant is adsorbed aluminum
(A1+) phosphate or aluminum hydroxyphosphate. Typically, the total aluminum
content is 200-1000 mg, 300-900 mg, 400-800 mg, 500-700 mg or around 630mg A1+
per 0.5 mL dose, which may be all aluminum hydroxide or all aluminum
phosphate. Alternatively Al + content may be from a mixture of aluminum
hydroxide and aluminum phosphate in various ratios, e.g., 1:8-8:1, 1:4-4:1, 3:8-8:3,
1:2-2:1 or 1:1 of aluminum phosphate: aluminum hydroxide. Although most
aluminum is provided by preadsorbed antigens before mixture to form a
combination vaccine, some aluminum may be added in free form during
formulation of the combination vaccine of the invention, e.g. before the pH
adjustment step described herein. Typically, free aluminum content per 0.5 mL
dose may be 0-300 mg, 50-250 mg, 75-200 mg, 100-150mg or around 120 mg of A13+.
Free A13+ may be all Al(OH)3 or all A1P04, or a mixture of Al(OH) 3 and A1P04
in various ratios.
[0050] Vaccine antigenic components may be preadsorbed onto an aluminum salt
individually prior to mixing. In another embodiment, a mix of antigens may be
preadsorbed prior to mixing with further adjuvants. Alternatively certain
components of the vaccines of the invention may be formulated but not
intentionally adsorbed onto adjuvant.
[0051] Formulations of the invention may further comprise one or more of a
buffer, a salt, a divalent cation, a non-ionic detergent, a cryoprotectant such as a
sugar, and an anti-oxidant such as a free radical scavenger or chelating agent, or
any multiple combination thereof. The choice of any one component, e.g., a
chelator, may determine whether or not another component (e.g., a scavenger) is
desirable. The final composition formulated for administration should be sterile
and/or pyrogen free. The skilled artisan may empirically determine which
combinations of these and other components will be optimal for inclusion in the
preservative containing vaccine compositions of the invention depending on a
variety of factors such as the particular storage and administration conditions
required.
[0052] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more physiologically
acceptable buffers selected from, but not limited to, Tris (trimethamine),
phosphate, acetate, borate, citrate, glycine, histidine and succinate. In certain
embodiments, the formulation is buffered to within a pH range of about 6.0 to
about 9.0, preferably from about 6.4 to about 7.4.
[0053] In certain embodiments, it may be desirable to adjust the pH of the
immunogenic composition or formulation of the invention. The pH of a
formulation of the invention may be adjusted using standard techniques in the art.
The pH of the formulation may be adjusted to be between 3.0 and 8.0. In certain
embodiments, the pH of the formulation may be, or may adjusted to be, between
3.0 and 6.0, 4.0 and 6.0, or 5.0 and 8.0. In other embodiments, the pH of the
formulation may be, or may adjusted to be, about 3.0, about 3.5, about 4.0, about
4.5, about 5.0, about 5.5, about 5.8, about 6.0, about 6.5, about 7.0, about 7.5, or
about 8.0. In certain embodiments, the pH may be, or may adjusted to be, in a
range from 4.5 to 7.5, or from 4.5 to 6.5, from 5.0 to 5.4, from 5.4 to 5.5, from 5.5
to 5.6, from 5.6 to 5.7, from 5.7 to 5.8, from 5.8 to 5.9, from 5.9 to 6.0, from 6.0 to
6.1, from 6.1 to 6.2, from 6.2 to 6.3, from 6.3 to 6.5, from 6.5 to 7.0, from 7.0 to
7.5 or from 7.5 to 8.0. In a specific embodiment, the pH of the formulation is
about 5.8.
[0054] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more divalent cations,
including but not limited to MgCl2, CaCl2 and MnCl2, at a concentration ranging
from about 0.1 mM to about 10 mM, with up to about 5 mM being preferred.
[0055] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more salts, including
but not limited to sodium chloride, potassium chloride, sodium sulfate, and
potassium sulfate, present at an ionic strength which is physiologically acceptable
to the subject upon parenteral administration and included at a final concentration
to produce a selected ionic strength or osmolarity in the final formulation. The
final ionic strength or osmolality of the formulation will be determined by multiple
components (e.g., ions from buffering compound(s) and other non-buffering salts.
A preferred salt, NaCl, is present from a range of up to about 250 mM, with salt
concentrations being selected to complement other components (e.g., sugars) so
that the final total osmolality of the formulation is compatible with parenteral
administration (e.g., intramuscular or subcutaneous injection) and will promote
long term stability of the immunogenic components of the vaccine formulation
over various temperature ranges. Salt-free formulations will tolerate increased
ranges of the one or more selected cryoprotectants to maintain desired final
osmolarity levels.
[0056] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more cryoprotectants
selected from but not limited to disaccharides (e.g., lactose, maltose, sucrose or
trehalose) and polyhydroxy hydrocarbons (e.g., dulcitol, glycerol, mannitol and
sorbitol).
[0057] In certain embodiments, the osmolarity of the formulation is in a range of
from about 200 mOs/L to about 800 mOs/L, with a preferred range of from about
250 mOs/L to about 500 mOs/L, or about 300 mOs/L - about 400 mOs/L. A saltfree
formulation may contain, for example, from about 5% to about 25% sucrose,
and preferably from about 7% to about 15%, or about 10%> to about 12% sucrose.
Alternatively, a salt-free formulation may contain, for example, from about 3% to
about 12% sorbitol, and preferably from about 4% to 7%, or about 5% to about 6%
sorbitol. If salt such as sodium chloride is added, then the effective range of
sucrose or sorbitol is relatively decreased. These and other such osmolality and
osmolarity considerations are well within the skill of the art.
[0058] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more free radical
oxidation inhibitors and/or chelating agents. A variety of free radical scavengers
and chelators are known in the art and apply to the formulations and methods of
use described herein. Examples include but are not limited to ethanol, EDTA, a
EDTA/ethanol combination, triethanolamine, mannitol, histidine, glycerol, sodium
citrate, inositol hexaphosphate, tripolyphosphate, ascorbic acid/ascorbate, succinic
acid/succinate, malic acid/maleate, desferal, EDDHA and DTPA, and various
combinations of two or more of the above. In certain embodiments, at least one
non-reducing free radical scavenger may be added at a concentration that
effectively enhances long term stability of the formulation. One or more free
radical oxidation inhibitors/chelators may also be added in various combinations,
such as a scavenger and a divalent cation. The choice of chelator will determine
whether or not the addition of a scavenger is needed.
[0059] In certain embodiments, a formulation of the invention which is
compatible with parenteral administration comprises one or more non-ionic
surfactants, including but not limited to polyoxyethylene sorbitan fatty acid esters,
Polysorbate-80 (Tween 80), Polysorbate-60 (Tween 60), Polysorbate-40 (Tween
40) and Polysorbate-20 (Tween 20), polyoxyethylene alkyl ethers, including but
not limited to Brij 58, Brij 35, as well as others such as Triton X-100; Triton X-
114, NP40, Span 85 and the Pluronic series of non-ionic surfactants (e. g. ,
Pluronic 121), with preferred components Polysorbate-80 at a concentration from
about 0.001% to about 2% (with up to about 0.25% being preferred) or
Polysorbate-40 at a concentration from about 0.001% to 1% (with up to about
0 .5% being preferred).
[0060] In certain embodiments, a formulation of the invention comprises one or
more additional stabilizing agents suitable for parenteral administration, e.g., a
reducing agent comprising at least one thiol (-SH) group (e.g., cysteine, N-acetyl
cysteine, reduced glutathione, sodium thioglycolate, thiosulfate, monothioglycerol,
or mixtures thereof). Alternatively or optionally, preservative-containing vaccine
formulations of the invention may be further stabilized by removing oxygen from
storage containers, protecting the formulation from light (e.g., by using amber
glass containers).
[0061] Preservative-containing vaccine formulations of the invention may
comprise one or more pharmaceutically acceptable carriers or excipients, which
includes any excipient that does not itself induce an immune response. Suitable
excipients include but are not limited to macromolecules such as proteins,
saccharides, polylactic acids, polyglycolic acids, polymeric amino acids, amino
acid copolymers, sucrose (Paoletti et al, 2001, Vaccine, 19:21 18), trehalose, lactose
and lipid aggregates (such as oil droplets or liposomes). Such carriers are well
known to the skilled artisan. Pharmaceutically acceptable excipients are discussed,
e.g., in Gennaro, 2000, Remington: The Science and Practice of Pharmacy, 20th
edition, ISBN:0683306472.
[0062] Compositions of the invention may be lyophilized or in aqueous form, i.e.
solutions or suspensions. Liquid formulations may advantageously be
administered directly from their packaged form and are thus ideal for injection
without the need for reconstitution in aqueous medium as otherwise required for
lyophilized compositions of the invention.
[0063] In particular embodiments of the present invention, the vaccine is a
multivalent immunogenic composition comprising one or more pneumococcal
capsular polysaccharides selected from serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14,
18C, 19A, 19F and 23F, individually conjugated to CRM197. The vaccine is
formulated to comprise: from 1 to 5 mg, preferably about 4.4 mg/mL of each
polysaccharide but preferably about 8.8 mg/mL of 6B; from 20 to 100 mg/mL,
preferably about 58 mg/mL CRM197 carrier protein; from 0.02 to 2 mg/mL,
preferably 0.25 mg/mL of elemental aluminum in the form of aluminum
phosphate; from 0.5 to 1.25%, preferably about 0.85%> sodium chloride; from
0.002 to 0.2 %, preferably about 0.02% polysorbate 80; from 1 to 10 mM,
preferably about 5 mM sodium succinate buffer at a pH from 4 to 7, preferably at a
pH of 5.8; and from 4 to 20 mg/mL, preferably about 10 mg/mL of 2-
phenoxyethanol.
[0064] In certain preferred embodiments of the present invention, the vaccine is a
multivalent immunogenic composition comprising pneumococcal capsular
polysaccharides from serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and
23F, individually conjugated to CRM197. The vaccine is formulated to comprise:
about 4.4 mg/mL of each saccharide, except for 6B at about 8.8 mg/mL; about 58
mg/mL CRM 1 carrier protein; about 0.25 mg/mL of elemental aluminum in the
form of aluminum phosphate; about 0.85%> sodium chloride; about 0.02%>
polysorbate 80; about 5 mM sodium succinate buffer at a pH of 5.8; and about 10
mg/mL of 2-phenoxyethanol.
[0065] The amount of many of the materials which the composition of the
invention may comprise can be expressed as weight/dose, weight/volume, or % >
concentration (as weight/volume or weight/weight). All of these values may be
converted from one to another. For conversions to and from a weight/dose unit, a
volume of the dose is specified. For example, given a dose of 0.5 mL, 5.0 mg/dose
2-PE is equivalent to a concentration of 10 mg/mL or 1.0% (g/lOOmL).
[0066] The formulation of the vaccine may also be expressed as a ratio of
polysaccharide:2-PE. For example, a 0.5 mL dose of the preferred formulation of
4.4 mg/mL of each saccharide, except for 6B at 8.8 mg/mL, and 10 mg/mL 2-PE
will have 30.8 mg polysaccharide (2.2 mg x 12 serotypes + 4.4 mg for serotype 6B)
and 5000 mg 2-PE. Therefore the weight ratio of polysaccharide :2-PE is
30.8:5000.
[0067] In certain embodiments of the invention, the polysaccharide: 2-PE weight
ratio of the vaccine is from 5:5000 to 100:5000. In a preferred embodiment of the
invention, said polysaccharide :2-PE weight ratio is about 30.8:5000.
Delivery of Vaccine Formulations
[0068] Also provided are methods of using the disclosed pharmaceutical
compositions and formulations comprising at least one preservative to induce an
immune response against pneumococcus in a mammalian subject, such as a human
subject, preferably in a child or infant, and to thereby protect against infection.
The vaccine formulations of the present invention may be used to protect a human
subject susceptible to pneumococcal infection, by administering the vaccine via a
systemic or mucosal route. These administrations may include, e.g., parenteral
administration or mucosal administration to the oral/alimentary, respiratory or
genitourinary tracts.
[0069] Direct delivery of vaccine preparations of the present invention to a
subject may be accomplished by parenteral administration (intramuscularly,
intraperitoneally, intradermally, subcutaneously, intravenously, or to the interstitial
space of a tissue); or by rectal, oral, vaginal, topical, transdermal, intranasal,
ocular, aural, pulmonary or other mucosal administration. In a preferred
embodiment, parenteral administration is by intramuscular injection, e.g., to the
thigh or upper arm of the subject. Injection may be via a needle (e.g. a hypodermic
needle), but needle free injection may alternatively be used. A typical
intramuscular dose is 0.5mL. Compositions of the invention may be prepared in
various forms, e.g., for injection either as liquid solutions or suspensions. In
certain embodiments, the composition may be prepared as a powder or spray for
pulmonary administration, e.g. in an inhaler. In other embodiments, the
composition may be prepared as a suppository or pessary, or for nasal, aural or
ocular administration, e.g. as a spray, drops, gel or powder.
[0070] In one embodiment, intranasal administration may be used for prevention
of pneumonia or otitis media (as nasopharyngeal carriage of pneumococci can be
more effectively prevented, thus attenuating infection at its earliest stage).
[0071] The amount of conjugate in each vaccine dose is selected as an amount
that induces an immunoprotective response without significant, adverse effects.
Such amount can vary depending upon the pneumococcal serotype. Generally,
each dose will comprise 0.1 to 100 mg of polysaccharide, particularly 0.1 to 10 mg,
and more particularly 1 to 5 mg.
[0072] Optimal amounts of components for a particular vaccine may be
ascertained by standard studies involving observation of appropriate immune
responses in subjects. Following an initial vaccination, subjects can receive one or
several booster immunizations adequately spaced.
[0073] The routine schedule for infants and toddlers against invasive disease
caused by S. Pneumoniae due to the serotypes included in the Prev(e)nar 13
vaccine is 2, 4, 6 and 12-15 months of age. Compositions of the present invention
are also suitable for use with older children, adolescents, teens and adults in which
the same or different routine schedules may apply, as determined by the skilled
professional.
Packaging and Dosage Forms
[0074] Vaccines of the invention may be packaged in unit dose or multi-dose
form (e.g. 2 doses, 4 doses, or more). For multi-dose forms, vials are typically but
not necessarily preferred over pre-filled syringes. Suitable multi-dose formats
include but are not limited to: 2 to 10 doses per container at 0.1 to 2 mL per dose.
In certain embodiments, the dose is a 0.5 mL dose. See, e.g., International Patent
Application WO2007/127668, which is incorporated by reference herein.
Compositions may be presented in vials or other suitable storage containers, or
may be presented in pre-filled delivery devices, e.g., single or multiple component
syringes, which may be supplied with or without needles. A syringe typically but
need not necessarily contains a single dose of the preservative-containing vaccine
composition of the invention, although multi-dose, pre-filled syringes are also
envisioned. Likewise, a vial may include a single dose but may alternatively
include multiple doses.
[0075] Effective dosage volumes can be routinely established, but a typical dose
of the composition for injection has a volume of 0.5 mL. In certain embodiments,
the dose is formulated for administration to a human subject. In certain
embodiments, the dose is formulated for administration to an adult, teen,
adolescent, toddler or infant (i.e., no more than one year old) human subject and
may in preferred embodiments be administered by injection.
[0076] Liquid vaccines of the invention are also suitable for reconstituting other
vaccines which are presented in lyophilized form. Where a vaccine is to be used
for such extemporaneous reconstitution, the invention provides a kit with two or
more vials, two or more ready-filled syringes, or one or more of each, with the
contents of the syringe being used to reconstitute the contents of the vial prior to
injection, or vice versa.
[0077] Alternatively, vaccine compositions of the present invention may be
lyophilized and reconstituted, e.g., using one of a multitude of methods for freeze
drying well known in the art to form dry, regular shaped (e.g., spherical) particles,
such as micropellets or microspheres, having particle characteristics such as mean
diameter sizes that may be selected and controlled by varying the exact methods
used to prepare them. The vaccine compositions may further comprise an adjuvant
which may optionally be prepared with or contained in separate dry, regular shaped
(e.g., spherical) particles such as micropellets or microspheres. In such
embodiments, the present invention further provides a vaccine kit comprising a
first component that includes a stabilized, dry vaccine composition, optionally
further comprising one or more preservatives of the invention, and a second
component comprising a sterile, aqueous solution for reconstitution of the first
component. In certain embodiments, the aqueous solution comprises one or more
preservatives, and may optionally comprise at least one adjuvant (see, e.g.,
WO2009/109550 (incorporated herein by reference).
[0078] In yet another embodiment, a container of the multi-dose format is
selected from one or more of the group consisting of, but not limited to, general
laboratory glassware, flasks, beakers, graduated cylinders, fermentors, bioreactors,
tubings, pipes, bags, jars, vials, vial closures (e.g., a rubber stopper, a screw on
cap), ampoules, syringes, dual or multi-chamber syringes, syringe stoppers, syringe
plungers, rubber closures, plastic closures, glass closures, cartridges and disposable
pens and the like. The container of the present invention is not limited by material
of manufacture, and includes materials such as glass, metals (e.g., steel, stainless
steel, aluminum, etc.) and polymers (e.g., thermoplastics, elastomers,
thermoplastic-elastomers). In a particular embodiment, the container of the format
is a 5 mL Schott Type 1 glass vial with a butyl stopper. The skilled artisan will
appreciate that the format set forth above is by no means an exhaustive list, but
merely serve as guidance to the artisan with respect to the variety of formats
available for the present invention. Additional formats contemplated for use in the
present invention may be found in published catalogues from laboratory equipment
vendors and manufacturers such as United States Plastic Corp. (Lima, OH), VWR.
Methodsfor Evaluating Preservative Efficacy in Vaccine Compositions
[0079] The present invention further provides novel methods for measuring the
efficacy of a vaccine formulation comprising one or more select preservative
agents in the presence of some or all of the immunogenic and non- immunogenic
components of the vaccine composition. The WHO Protocol on preservative
efficacy utilizes USP and EP tests and include Open Vial Policy conditions when
performing certain tests. A typical preservative efficacy test is a single challenge
test in which a test composition is inoculated one time with a select micro
organism population and the log reduction of inoculated micro-organism over time
and under particular environmental conditions (e.g., temperature) is compared to
the log reduction of inoculated micro-organism in a control composition lacking
the test preservative(s). See, e.g., Examples 2 and 3, below. However, no
additional tests have been required to address preservative efficacy upon multiple
contaminations, e.g., to address vials and stoppers by inoculating the same vials
multiple times.
[0080] Accordingly, the invention provides a multi-challenge test for evaluating
the efficacy of one or more preservatives in an immunogenic composition, wherein
the test comprises at least two steps of inoculating the test composition with a
select micro-organism population and comparing the reduction of inoculated
micro-organism(s) over time and under particular environmental conditions (e.g.,
temperature) to the reduction in a control composition lacking the test
preservative(s). See Examples 4 and 5, below.
Preservative effectiveness
[0081] Preservative-containing vaccine formulations of the present invention are
suitable for filling in a multi-dose vaccine vial or container compatible with, e.g.,
parenteral administration, and remain stable for extended periods of time at 2-8°C,
room temperature or 37°C with reduced or negligible loss of activity when
compared to the same formulation lacking preservative(s).
[0082] The amount of preservative in the formulation is selected to be an amount
that fulfills requirements for vaccine safety, as defined by the United States (U.S.),
European or World Health Organization (WHO) Pharmacopeias, or a combination
thereof.
[0083] For ascertaining preservative levels according to U.S. and European
Pharmacopeias (USP and EP, respectively), the vaccine formation is inoculated
once with approximately 105 to 10 CFU/ml at time 0 (CFU = colony forming
units) of:
1. Staphylococcus aureus (Bacteria; ATCC # 6538; "SA")
2. Pseudomonas aeruginosa (Bacteria; ATCC # 9027; "PA")
3. Candida albicans (Yeast; ATCC# 10231; "CA")
4. Aspergillus niger (Mold; ATCC # 16404; "AN")
[0084] To represent the worst reasonable case of contamination that may occur in
practice during the repeated use of a multi-dose presentation, WHO requires safety
testing with deliberate exposure to multiple contamination events using bacterial
strains, Pseudomonas Aeruginosa ("PA"), Staphylococcus Aureus ("SA"),
Escherichia coli ("EC") and Bacillus subtilis ("BA" Formulations are spiked
with 5 x 10 CFU/ml of each organism at times 0, 6 hours, 24 hours, 7 days and 14
days after initial challenge and stored either at 2 - 8°C or at 22 - 24 °C to mimic
the potential storage conditions in practice.
[0085] USP 29 NF 24 Supplement 2 (USP) requires that, after an inoculation of
bacterial micro-organism(s), there is at least 1.0 log reduction from the initial
calculated count (i.e., at time of inoculation) at 7 days, at least 3.0 log reduction at
14 days from the previous value measured, and no increase at 28 days compared to
the previous value measured. See Table 1. For yeast and fungi, the USP
requirement is for there to be no increase from time of inoculation at 7, 14 and 28
days.
5 [0086] EP requirements are more stringent. EP 5th Edition 5.6 (5.1.3)
requirements for parenteral and ophthalmic preparations has two components:
Category A and Category B. Category A (EP-A) requires, for bacteria, at least 2.0
log reduction from the initial calculated count at 6 hours after inoculation, at least
3.0 log reduction from the previous value measured at 24 hours and no recovery at
10 28 days. Category B (EP-B) requires, for bacteria, at least 1.0 log reduction from
the initial calculated count at 24 hours, at least 3.0 log reduction at 7 days from the
previous value measured and not more than 0.5 log increase from the previous
value measured (i.e., no increase) at 28 days. See Table 1. For yeast and fungi,
Category A requires at least 2.0 log reduction at 7 days from the initial calculated
15 count, and no increase at 28 days from the previous measured value; and Category
B requires at least 1.0 log reduction from the initial calculated count at 14 days and
no increase at 28 days from the previous measured value.
Table 1: Acceptance Criteria for Preservative Effectiveness Test Between United States,
European and Japanese Pharmacopeias
Log CFU/mL reduction
Organisms Method
6 h 24 h 7 d 14 d 28 d
Bacteria EP A* 2 3 - - ***
EP B - 1 3 - *
USP - - 1 3 NI
JP - - - 3 NI
Yeast and
EP A - - 2 - NI
Fungi
EP B - - - 1 NI
USP - - NI NI NI
JP - - - NI NI
* The A criteria express the recommended efficacy to be achieved. In justified cases, where the A criteria can not
be attained, the B criteria must be satisfied.
** NI: No increase: It is defined as not more than 0.5 logio unit higher than the previous value measured.
*** NR: No recovery
[0087] In certain embodiments of the present invention, a preservative of the
invention is effective in reducing the concentration of micro-organisms in the
immunogenic formulation. In certain embodiments of the invention, the vaccine
formulation, comprising at least one preservative, reduces the concentration of one
or more micro-organisms following inoculation with said micro-organisms
compared to the vaccine formulation without the one or more preservatives. In a
particular embodiment of the invention, the formulation presents at least 1.0 log
reduction from the initial micro-organism count at 24 hours, at least 3.0 log
reduction at 7 days from the previous value measured and not more than 0.5 log
increase at 28 days from the previous value measured. In another particular
embodiment of the invention, the formulation presents at least 2.0 log reduction
from the initial calculated count at 6 hours after inoculation, at least 3.0 log
reduction at 24 hours from the previous value measured and no recovery at 28
days, compared from the initial micro-organism count. In another embodiment of
the invention, the formulation meets European Pharmacopeia (EP) requirements
for parenteral and ophthalmic preparations, in particular Category A (EP-A)
and/or Category B (EP-B) of the EP 5th Edition 5.6 (5.1.3) requirements. In
another embodiment of the invention, the formulation meets United States
Pharmacopeia (USP) 29 NF 24 Supplement 2 requirements for parenteral
preparations.
[0088] In certain embodiments of the invention, the at least one preservative of
the invention is effective in reducing the concentration of micro-organisms in the
formulation when challenged with micro-organisms compared to a formulation
lacking the one or more preservatives. The micro-organisms may be, without
limitation, one or more of the following: Pseudomonas aeruginosa,
Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Candida albicans
Aspergillus niger and others.
[0089] In certain embodiments of the invention, the micro-organisms may be
introduced or inoculated into the vaccine one or more times at various intervals.
The inoculation may occur in the context of a deliberate experimental inoculation
or in the context of a contaminated hypodermic needle entering a container of a
multi-dose vaccine formulation. The interval between inoculations may be
between 1 minute and 1 month. In a particular embodiment, the multiple
inoculations occur, following an initial inoculation, at 6 hours following the initial
inoculation, at 24 hours following the initial inoculation, at 7 days following the
initial inoculation and at 14 days following the initial inoculation.
Parametersfor vaccine andpreservative stability
[0090] In certain embodiments of the present invention, the antigenicity of at
least one antigenic determinant (i.e., polysaccharide preparation from a
Streptococcus pneumoniae serotype) in the vaccine formulation is stable for a
range of storage times and temperatures. The antigenicity may be measure by
methods known in the art. For example, total antigenicity may be determined by
using type-specific anti-sera, as described in Example 3.
[0091] In certain embodiments of the present invention, the antigenicity of at least
one antigenic determinant in the vaccine formulation is stable for not less than 4
weeks, not less than 6 weeks, not less than 8 weeks, not less than 10 weeks, not
less than 12 weeks, not less than 18 weeks, not less than 24 weeks, not less than 48
weeks, not less than 1 year, not less than 1.25 years, not less than 1.5 years, not
less than 1.75 years, not less than 2 years, not less than 2.25 years, or not less than
2.5 years. Preferably, the antigenicity of a plurality of antigenic determinants, e.g.,
at least 50%, 75%, 80%, 85%, 90%, 95% or more, of the antigenic determinants in
the vaccine in the formulation are stable for not less than 4 weeks, not less than 6
weeks, not less than 8 weeks, not less than 10 weeks, not less than 12 weeks, not
less than 18 weeks, not less than 24 weeks, not less than 48 weeks, not less than 1
year, not less than 1.25 years, not less than 1.5 years, not less than 1.75 years, not
less than 2 years, not less than 2.25 years, or not less than 2.5 years.
[0092] In certain embodiments of the present invention, antigenicity of at least
one antigenic determinant in the vaccine formulation is stable when stored at about
-25°C to about 37°C, or -20 to -10 °C, or 2 to 8 °C, or about room temperature, or
22 °C to 28 °C , or about 37 °C. In a particular embodiment of the invention,
antigenicity of at least one antigenic determinant in the vaccine formulation is
stable after storage for not less than 2.5 years at a temperature of 2 to 8 °C.
[0093] In certain embodiments of the present invention, the concentration of the
preservative of the invention is stable after storage of the vaccine at the abovementioned
durations and storage temperatures. In a particular embodiment of the
invention, the concentration of the preservative in the vaccine formulation is stable
after storage of the vaccine for not less than 2.5 years at a temperature of 2 to 8 °C.
The concentration of the preservative may be measure by methods known in the
art. For example, Thimerosal may be measured using Cold Vapor Atomic
Absorption Spectrometry (CVAAS), as described in Example 3. 2-EP
concentration may be measured with a Reversed-Phase HPLC assay, also as
described in Example 3. A Reversed-Phase HPLC assay may be performed in the
following manner: Samples are vortexed and diluted 1:10 into 5 mM Succinate
buffer in saline, centrifuged and diluted again 1:10 into 5 mM succinate buffer in
saline (final dilution of the Test Sample is 1:100). The sample is then assayed
utilizing the Agilent Eclipse XDB-C18 HPLC column and a linear gradient of
water and acetonitrile containing trifluoroacetic acid. The quantification of the
preservative is then compared to a standard curve. See also, Sharma et al,
Biologicals 36(1): 6 1 - 63 (2008).
[0094] The above disclosure generally describes the present invention. A more
complete understanding may be obtained by reference to the following specific
examples. These examples are described solely for the purpose of illustration and
are not intended to limit the scope of the invention.
EXAMPLES
Example 1 - Preliminary preservative screening study
[0095] Formulation development of multi-dose Prev(e)nar 13 vaccine started
with preliminary screening of preservatives, including Phenol (0.25%), 2-
Phenoxyethanol (5 mg/mL), Meta-Cresol (0.3%), Methylparaben and
Propylparaben (0.18% and 0.12%, respectively) in Prev(e)nar 13 formulations.
[0096] To test for preservative effectiveness, aliquots of vaccine were inoculated
with the following organisms:
1. Staphylococcus aureus (Bacteria; ATCC # 6538)
2. Pseudomonas aeruginosa (BacteriaATCC # 9027)
3. Candida albicans (Yeast; ATCC# 10231)
4. Aspergillus niger (Mold; ATCC # 16404)
Thirty milliliters (ml) of each vaccine formulation with and without Thimerosal or
2-PE at indicated concentrations or saline containing Thimerosal at 0.02% were
inoculated in triplicates with a suspension of each test organism to achieve an
inoculum density of approximately 105 to 106 CFU/ml at time 0 (CFU = colony
forming units). The volume of each inoculum did not exceed 1% of the volume of
the product during each deliberate challenge. Samples were mixed to ensure even
distribution of challenged organisms. Another 30 ml of vaccine in triplicate (with
and without preservative) were used as a negative control and spiked with the
culture media alone to evaluate the inherent contamination that might be present in
the sample or media. Each of the three series of vaccines, and positive and
negative controls, was then separately incubated at 20 to 25°C. Aliquots ( 1 ml) of
the challenged samples and controls (or their appropriate serial ten fold dilutions)
were enumerated by plate count in duplicates at time 0 and at intervals of 6 hours,
24 hours, 7 days, 14 days and 28 days post-inoculation.
[0097] USP 29 NF 24 Supplement 2 (USP) requires that, after an inoculation of
bacterial micro -organism(s), there is at least 1.0 log reduction from the initial
calculated count (i.e., at time of inoculation) at 7 days, at least 3.0 log reduction at
14 days from the previous value measured and no increase at 28 days from the
previous measured value. See Table 1. For yeast and fungi, the USP requirement
is for there to be no increase from the time of inoculation to 7, 14 and 28 days.
[0098] EP requirements are more stringent. EP 5th Edition 5.6 (5.1.3)
requirements for parenteral and ophthalmic preparations has two components:
Category A and Category B. Category A (EP-A) requires, for bacteria, at least 2.0
log reduction from the initial calculated count at 6 hours after inoculation, at least
3.0 log reduction at 24 hours from the previous measured value, and no recovery at
28 days. Category B (EP-B) requires, for bacteria, at least 1.0 log reduction at 24
hours from the initial calculated count, at least 3.0 log reduction at 7 days from the
previous value measured and not more than 0.5 log increase at 28 days from the
previous value measured (i.e., no increase). See Table 1. For yeast and fungi,
Category A requires at least 2.0 log reduction at 7 days and no increase from the
previous value measured at 28 days, and Category B requires at least 1.0 log
reduction at 14 days and no increase from the previous value measured at 28 days.
[0099] Plates containing <300 CFU for bacteria or <100 CFU for yeast or mold
were used during enumeration. For single challenge studies, arithmetic average
count of all surviving micro-organisms in triplicate and on duplicate plates (6 values
per time point) plus their diluted samples were measured and normalized as CFU/ml.
The results are expressed as mean logio CFU/ml reduction (compared to time 0). In
this case, the count of surviving micro-organisms is evaluated at time 0 as the
baseline and compared to incubation time of 6 hours, 24 hours, 7 days, 14 days and
28 days.
[0100] The preservatives tested showed no obvious impact on Prev(e)nar 13
stability except for the parabens (methylparaben and propylparaben), which
showed a decreased in Prev(e)nar 13 bound antigenicity. Further, phenol, metacresol,
methyl- and propylparabens interfered with the Modified Lowry protein
assay (protein concentration of the vaccine is determined by the commercial
available Modified Lowry protein assay).
[0101] Preservative effectiveness test (PET) results showed that all of the tested
preservatives met the USP requirements but not the EP criteria (EP-A or EP-B).
See Table 2. 2-PE was the only candidate preservative which was known to be
safe at higher dosages. Therefore, further tests on preservative effectiveness, with
higher doses of 2-PE, were pursued.
Table 2 : The effectiveness of potential preservatives in meeting USP and EP*
vaccine safet re uirements after a sin le challen e of micro-organisms
* EP-B
Example 2 - Preservative effectiveness test by single challenge method: 2-PE
and Thimerosal
[0102] Thimerosal at 0.01% concentration is commonly used in major vaccines
licensed in the U.S. The effectiveness of Thimerosal as a preservative was tested
using the same single-challenge method described above in Example 1. Prev(e)nar
13 vaccine formulation containing Thimerosal at 0.01% (equivalent to 25mg
mercury per 0.5 mL dose) did not meet the European acceptance criteria EP-A or
EP-B established by preservative anti-microbial effectiveness method of EP. It
however, did pass acceptance limits established by the U.S. or Japanese
Pharmacopoeia, since the acceptance limits established by these compendial
methods are less stringent compared to that established in EP. See Figure 1.
[0103] Thimerosal at 0.02% (containing 50mg mercury per dose), which is
equivalent to twice the recommended concentration of Thimerosal in some of the
U.S. licensed vaccines, or at 0.04%> (containing 100mg mercury per dose), which is
equivalent to four times the recommended concentration of Thimerosal in some of
the U.S. licensed vaccines, met the EP acceptance criteria B, but not the more
stringent A acceptance criteria (with a single challenge of micro-organisms). See
Figure 1.
[0104] 2-PE was more effective as a preservative than Thimerosal. While 2-PE
at 2.5 mg/dose failed both EP acceptance criteria A and B, 2-PE at concentrations
of 3.5 to 5.5 mg/dose met EP acceptance criteria B. At concentrations above 6.0
mg/dose, 2-PE met both EP-A and EP-B anti-microbial effectiveness acceptance
criteria (Figure 2).
Example 3 - Single challenge method with 2-PE and Thimerosal: Change in
Contaminant Level
[0105] Absence of preservatives in the Prev(e)nar 13 vaccine formulation
resulted in a slow growth of P. aeruginosa, no change to C. albicans levels and A.
niger and slow reduction in colony forming units of S. aureus over a 28 days
challenged period at 20 - 25°C (Figure 3).
[0106] The presence of 0.01% Thimerosal (containing 25 mg mercury per dose)
reduced the contamination levels of all four inoculated micro-organisms.
However, the inhibition of S. aureus and C. albicans was weaker than the
inhibition of P. aeruginosa and A. niger (Figure 4). A dose response relationship
on the rate of anti-microbial effect of Thimerosal in Prev(e)nar 13 vaccine
formulations was seen, especially against C. albicans, with the reduction of
contamination levels being more pronounced with 0.02% Thimerosal (Figure 5).
Absence of Prev(e)nar 13 in a 0.02% Thimerosal-containing saline formulation
slightly improved the growth inhibitory effectiveness of Thimerosal against S.
aureus and C. albicans (Figure 6).
[0107] 2-PE was more effective as a preservative than Thimerosal. For example,
in contrast to the slow decline of S. aureus with Thimerosal, the anti-microbial
efficacy of 5.0 mg/dose 2-PE resulted in reduction of S. aureus to baseline in 24
hrs after inoculation (Figure 7). Although 2-PE was less effective than Thimerosal
as a preservative against A. niger (Figure 7), and the rate of decline of A. niger
contamination was slower compared to Thimerosal (Figures 4 and 5), the superior
effectiveness of 2-PE with regard to the other strains allowed it to meet the
preservative acceptance criteria EP-B at a concentration of 3.5 and 5 mg/dose
(Figure 2), while 0.01% Thimerosal did not (Figure 1).
[0108] The preservative effectiveness of 2-PE at 3.5 to 5.0 mg/dose remained
persistent when formulations were stored at 37°C for a month or at 2 - 8°C for two
and a half years (Figure 2). The concentration of 2-PE in the formulation was
similarly stable (Figure 15). The immunological activity (total antigenicity) of
each of the 13 serotypes present in the Prev(e)nar 13 formulation was also stable
under these storage conditions (Figure 14).
[0109] Total antigenicity was derived from both bound and unbound
polysaccharides present in the vaccine for each serotype. Type-specific
antigenicities were determined by using type-specific anti-sera. Prior to the assay,
the 13-valent vaccine formulated with aluminum phosphate was first solubilized.
The solution was then neutralized to avoid alkaline-induced degradation. Using a
Nephelometer, the assay measured the rate of change of light scattering intensity
derived from the antibody-antigen complex formation. Antigenicities of test
samples were determined by linear regression using standard curves measured
immediately before or after analysis of samples.
[0110] In order to assure of Thimerosal content of the Prev(e)nar 13 vaccine and
saline formulations, the concentration of mercury was determined in some of the
formulations by the method of Cold Vapor Atomic Absorption Spectrometry
(CVAAS). The measured concentration of mercury was very close to its predicted
values, suggesting that Thimerosal concentration in these formulations were on
target and not underestimated. The measured concentration of 2-PE was also very
close to its predicted value and did not change upon storage of Prev(e)nar 13
formulations over time at either 2-8°C or 37°C. 2-PE concentration was measured
with a Reversed-Phase HPLC assay. Samples were vortexed and diluted 1:10 into
5 mM Succinate buffer in saline, centrifuged and diluted again 1:10 into 5 mM
succinate buffer in saline. Final dilution of the Test Sample was 1:100. The assay
utilized the Agilent Eclipse XDB-C18 HPLC column and a linear gradient of water
and acetonitrile containing trifluoroacetic acid. 2-PE in 13vPnC Multi-Dose
Vaccine samples was quantified against a 2-PE standard curve. See also, Sharma
et al, Biologicals 36(1): 6 1 - 63 (2008).
Example 4 - Preservative effectiveness test by multi-challenge method:
Thimerosal
[0111] To assess the appropriateness of WHO multi-dose Open Vial Policy of
vaccines in multiple immunization sessions for up to maximum of four weeks,
experimental design provided by WHO was implemented. In this study, the
effectiveness of Thimerosal was evaluated at the concentration that is present in
the majority of U.S. licensed vaccines (0.01%), as well as at a higher concentration
of 0.02%. To represent the worst reasonable case of contamination that may occur
in practice during the repeated use of a multi-dose presentation, and to test WHO
requirements, Prev(e)nar 13 vaccine formulations with 0.01 or 0.02% Thimerosal
or with 5.0 mg/dose of 2-PE were deliberately exposed to multiple contamination
events using WHO recommended bacterial strains, P. aeruginosa, S. aureus, E.
coli and B. subtilis. Formulations were spiked with 5 x 10 CFU/ml of each
organism at times 0, 6 hours, 24 hours, 7 days and 14 days after initial challenge
and stored either at 2 - 8 °C or at 22 - 24 °C to mimic the potential storage
conditions in practice. Saline formulation containing 0.02% Thimerosal was also
used as a control to evaluate the potential impact of Prev(e)nar 13 on the
antimicrobial efficacy of Thimerosal in the formulation.
[0112] Upon multiple deliberate contaminations of Prev(e)nar 13 vaccine
formulation in the absence of a preservative, the level of P. aeruginosa and E. coli
organisms increased over the course of study, especially when stored at 22 - 24°C
(Figures 8A and 8B). The level of S. aureus in formulation stored at 22 - 24°C
slowly declined, similar to that observed during the single challenge study (Figure
8A compare to Figure 3). The viability of B. subtilis declined even more
noticeably (Figures 8A and 8B). These results suggest that B. subtilis is not a
robust organism in this formulation to be used as a model for such challenge
studies in preservative effectiveness test, despite it's recommendation by the WHO.
[0113] In the Prev(e)nar 13 vaccine formulation, the antibacterial effectiveness
of 0.01% Thimerosal was highest on B. subtilis followed by P. aeruginosa.
However, the reduction of S. aureus and E. coli was slow, particularly when the
formulations were stored at 2 - 8°C (Figures 9A and 9B).
[0114] As shown in the non- linear regression analysis of decay in the viability of
S. aureus is summarized in Figure 12, the rate of decay of S. aureus was
substantially slower (-5.98 logio decay per day, with 50%> decay in 30.28 days)
when formulation was stored at 2 - 8°C compared to that stored at 22 - 24°C (-1 .39
logio decay per day, with 50%> decay in 6.2 days) (Figure 12). These results show
that 0.01% Thimerosal in a Prev(e)nar 13 vaccine formulation, being contaminated
in the field during multi-dose delivery, and further stored at refrigerated
temperature, will not be effective in reducing bacterial contamination.
[0115] The effectiveness of Thimerosal was both concentration and temperature
dependent (Figures 9 and 10). Thimerosal was a more effective preservative at
the higher concentration of 0.02%. It was also a more effective preservative at the
higher storage temperature of 22 - 24°C. However, as discussed above, even with
0.02% concentration and 22-24°C storage, Thimerosal did not meet the EP
requirements of either EP-A or EP-B when such criteria were applied during the
multi-challenge studies (Figure 1).
[0116] To study whether or not the vaccine itself affects the preservative action
of Thimerosal, the effectiveness of 0.02% Thimerosal with multiple challenges
was compared between saline and the Prev(e)nar 13 vaccine formulation. In the
presence of 0.02%> Thimerosal, the rate of decay of both S. aureus and E. coli was
more pronounced in saline formulation than in the vaccine formulation (Figure 11
compare to Figure 10 and Figure 12), demonstrating that the presence of the
vaccine, to some extent, inhibited the effectiveness of Thimerosal as a
preservative. Nevertheless, even in a saline control formulation that did not
contain the vaccine, 0.02% Thimerosal still did not meet the acceptance criteria of
EP-A or EP-B when multiply challenged (Figure 1).
Example 5 - Preservative effectiveness test by multi-challenge method: 2-PE
[0117] In contrast to the lack of effectiveness of Thimerosal as a preservative,
especially when multiply inoculated or stored at 2 - 8 °C, Prev(e)nar 13 vaccine
formulation containing 5 mg/dose of 2-PE as the preservative results in a stronger
inactivation of S. aureus viability, regardless of challenge method (i.e., single or
multiple) or storage temperature (Figure 12).
[0118] In fact, with the multi-challenge method, regardless of the storage
temperature, and with all the organisms tested (P. aeruginosa, S. aureus, E. coli
and B. subtilis), 5 mg/dose 2-PE was superior as a preservative over 0.01%
Thimerosal. In a non-linear regression analysis of S. aureus decay in various
challenge studies, the vaccine formulations with 2-PE had a faster rate of microbial
contaminant decay than those with Thimerosal both in terms of 50% decay and
average slope of decay (logio decay/day). See Figure 12. Further, 5 mg/dose 2-PE
met the EP-B criteria under multiple challenge, while no version of Thimerosal
was able to do so under the same conditions (Figure 13).
[0119] Thimerosal is not an effective preservative in protecting Prev(e)nar 13 in
multi-dose formulation against potential contamination that may be introduced
during dispensation. This is even more evident when contamination is introduced
multiple times during dosing subjects in multi-dose formulations. Thimerosal has
a slow rate of inactivation, particularly against S. aureus and E. coli, with a lagging
immediate effect to clear the potential contaminating organisms when general
practitioners might withdraw vaccines from multi-dose vials under poor hygienic
conditions. However, 2-PE at 3.5 to 5 mg/dose is stable with a much higher rate of
antimicrobial effectiveness compared to Thimerosal and therefore will protect the
product from inadvertent contamination while dosing subjects.
Example 6 - Immune response elicited by immunization of Prevenar 13 with
or without 2-phenoxy ethanol as a preservative in nonhuman primates
The ability of Prevenar 13 and Prevenar 13 containing 2-phenoxy ethanol to induce
immune response is evaluated in cynomolgus macaques.
Two immunization groups of 10 macaques for a total of 20 cynomolgus macaques
are used for the study as detailed at Table 3.
Table 3
Prescreened animals are randomized into groups based on their body weights and
baseline titers.
Macaques are given the clinical dose of 13vPnC containing 0 or 5mg of 2-
phenoxyethanol as preservative. The vaccine is given intramuscularly at a single
site in the quadriceps muscle of each monkey. The final volume delivered is
0.5mL.
All macaques receive three doses and are vaccinated at week 2, 4 and 8.
Bleed Schedule: Peripheral blood is sampled at week 0, 6, 8, 10, 12 and 16 to
monitor the induction of immune responses to the vaccines.
Immune response elicited by vaccination is monitored by performing the below
assays on serum collected during the study:
• In vitro binding and functional antibodies:
o Serotype-specific IgG by ELISA (see e.g. Fernsten P, et al, Hum
Vaccin. 201 1 Jan l;7:75-84)
o Serotype-specific opsonophagocytosis assay (OPA) (see e.g.
Fernsten P, et al., Hum Vaccin. 201 1 Jan l;7:75-84)
• In vivo protection in the infant rat challenge model (see e.g. Fernsten P, et
al, Hum Vaccin. 201 1 Jan l;7:75-84):
o Pooled macaque sera is evaluated for serotype-specific protection.

Claims:
1. A multivalent immunogenic composition comprising a
plurality of capsular polysaccharides from Streptococcus pneumoniae serotypes 1,
3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F conjugated to a carrier protein,
and further comprising 2-phenoxyethanol (2-PE).
2. The multivalent immunogenic composition of claim 1,
wherein said composition comprises seven or more capsular polysaccharides from
Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F
and 23F.
3. The multivalent immunogenic composition of any one of
claim 1-2, wherein said composition comprises 2-PE at a concentration of between
7 mg/mL and 15 mg/mL.
4. The multivalent immunogenic composition of claim 3,
wherein said composition comprises 2-PE at a concentration of about 10 mg/mL.
5. The multivalent immunogenic composition of any one of
claims 1-4, wherein said composition comprises not less than 7 mg/mL of 2-PE.
6. The multivalent immunogenic composition of any one of
claims 1-4, wherein said composition comprises not less than 10 mg/mL of 2-PE.
7. The multivalent immunogenic composition of any one of
claims 1-4, wherein said composition comprises not less than 15 mg/mL of 2-PE.
8. The multivalent immunogenic composition of any one of
claims 1-7, wherein said composition further comprises and adjuvant, and wherein
said adjuvant is aluminum phosphate.
9. The multivalent immunogenic composition of any one of
claims 1-8, wherein the antigenicity of the immunogenic composition is stable for
not less than 1 year, 1.5 years, 2 years or 2.5 years.
10. The multivalent immunogenic composition of any one of
claims 1-9, wherein, following inoculation with one or more micro-organisms, the
concentration of said micro-organisms is reduced over time.
11. The multivalent immunogenic composition of claim 10,
wherein, following inoculation with one or more bacteria strains, the composition
presents at least 1.0 log reduction from the initial micro-organism count at 24
hours, at least 3.0 log reduction at 7 days from the previous value measured and
not more than 0.5 log increase at 28 days from the previous value measured.
12. The multivalent immunogenic composition of claim 10,
wherein, following inoculation with one or more bacteria strains, the composition
presents at least 2.0 log reduction from the initial calculated count at 6 hours after
inoculation, at least 3.0 log reduction at 24 hours from the previous value measured
and no recovery at 28 days.
13. The multivalent immunogenic composition of any one of
claims 10-12, wherein the micro-organism strains are one or more strains selected
from P . aeruginosa, S. aureus, E. coli and B. subtilis.
14. The multivalent immunogenic composition of any one of
claims 10-13, wherein the composition is inoculated multiple times.
15. The multivalent immunogenic composition of claim 13 or
14, wherein a second inoculation occurs at 6 hours following the initial
inoculation, a third inoculation occurs at 24 hours following the initial inoculation,
a third inoculation occurs at 7 days following the initial inoculation and a fourth
inoculation occurs at 14 days following the initial inoculation.
16. The multivalent immunogenic composition of any one of
claims 1-15, wherein said composition further comprises one or more of a buffer, a
cryoprotectant, a salt, a divalent cation, a non-ionic detergent, and an inhibitor of
free radical oxidation.
17. A multivalent immunogenic composition formulation of
pneumococcal capsular polysaccharides from serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V,
14, 18C, 19A, 19F and 23F, individually conjugated to CRM197, wherein the
multivalent immunogenic composition is formulated in a sterile liquid to comprise:
about 4.4 mg/mL of each polysaccharide, except for 6B at about 8.8 mg/mL; about
58 mg/mL CRM197 carrier protein; about 0.25 mg/mL of elemental aluminum in the
form of aluminum phosphate; about 0.85% sodium chloride; about 0.02%
polysorbate 80; about 5 mM sodium succinate buffer at a pH of 5.8; and about 10
mg/mL of 2-phenoxyethanol.
18. A vial containing a multivalent immunogenic composition
of any one of claims 1-17.
19. The vial of claim 18, wherein said vial contains more than
one dose of the immunogenic composition.
20. A pre-filled vaccine delivery device comprising a
multivalent immunogenic composition of any one of claims 1-19.
21. The pre-filled vaccine delivery device of claim 20, wherein
said device is or comprises a syringe.
22. The pre-filled vaccine delivery device of claim 19, wherein
said device is or comprises a dual or multiple chamber syringe or vials or
combinations thereof.
23. The pre-filled vaccine of claims 20-22, wherein said
multivalent immunogenic composition is formulated for intramuscular or
subcutaneous injection.
24. A kit for preparing the multivalent immunogenic
composition of any one of claimsl-17, wherein the kit comprises (i) said plurality
of capsular polysaccharides in a lyophilized form of the composition of any one of
the above claims, and (ii) aqueous material for reconstituting component (i) in
order to provide the aqueous composition.
25. A multi-dose vaccine comprising 4 doses of a vaccine in a
vial, each dose comprising from 4 to 20 mg/mL, preferably 10 mg/mL of 2-
phenoxyethanol, wherein a dose is 0.5 mL of vaccine.
26. A container comprising two doses or more,
at 0.1 to 2 mL per dose, of the multivalent immunogenic composition of any one of
claims 1-17.
27. The container of claim 26 wherein the dose is a
0.5 mL dose.
28. The container of claim 26-27 comprising 2 to 10 doses.
29. A method for measuring the efficacy of a vaccine
formulation comprising one or more select preservative agents in the presence of
some or all of the immunogenic and non-immunogenic components of the vaccine
composition, wherein the test comprises at least two steps of inoculating the test
composition with a select micro-organism population and comparing the log
reduction of inoculated micro -organism(s) over time and under particular
environmental conditions (e.g., temperature) to the log reduction in a control
composition lacking the test preservative(s