Label: VAXCHORA- cholera vaccine, live, oral

  • NDC Code(s): 70460-001-01, 70460-002-02, 70460-003-02
  • Packager: Paxvax, Inc.
  • Category: VACCINE LABEL
  • DEA Schedule: None
  • Marketing Status: Biologic Licensing Application

Drug Label Information

Updated January 10, 2017

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use VAXCHORA safely and effectively. See full prescribing information for VAXCHORA.
    VAXCHORA (Cholera Vaccine, Live, Oral)
    Suspension for Oral Administration
    Initial U.S. Approval: 2016

    INDICATIONS AND USAGE

    VAXCHORA is a vaccine indicated for active immunization against disease caused by Vibrio cholerae serogroup O1. VAXCHORA is approved for use in adults 18 through 64 years of age traveling to cholera-affected areas. (1)
     

    Limitations of Use:
     

    The effectiveness of VAXCHORA has not been established in persons living in cholera-affected areas. ( 1.1)
    The effectiveness of VAXCHORA has not been established in persons who have pre-existing immunity due to previous exposure to V. cholerae or receipt of a cholera vaccine. ( 1.1)
    VAXCHORA has not been shown to protect against disease caused by V. cholerae serogroup O139 or other non-O1 serogroups. ( 1.1)

    DOSAGE AND ADMINISTRATION

    For oral administration only.
    Prepare and administer VAXCHORA in a healthcare setting equipped to dispose of medical waste. ( 2.3)
    Prepare VAXCHORA by reconstituting the buffer component in 100 milliliters (mL) of purified bottled water; then add the active component (lyophilized V. cholerae CVD 103-HgR). ( 2.3) After preparation, a single dose of VAXCHORA is 100 mL. ( 3)
    Instruct recipients to avoid eating or drinking for 60 minutes before or after oral ingestion of VAXCHORA. ( 2.2)
    Administer VAXCHORA a minimum of 10 days before potential exposure to cholera. ( 2.1)

    DOSAGE FORMS AND STRENGTHS

    Suspension for oral administration supplied as a packet of the buffer component and a packet of the active component (lyophilized V. cholerae CVD 103-HgR). After preparation, a single dose of VAXCHORA is 100 mL. (3)

    CONTRAINDICATIONS

    Severe allergic reaction (e.g., anaphylaxis) to any ingredient of VAXCHORA or to a previous dose of any cholera vaccine. (4)

    WARNINGS AND PRECAUTIONS

    The safety and effectiveness of VAXCHORA have not been established in immunocompromised persons. ( 5.1)
    VAXCHORA may be shed in the stool of recipients for at least 7 days. There is a potential for transmission of the vaccine strain to non- vaccinated close contacts (e.g., household contacts). Use caution when considering whether to administer VAXCHORA to individuals with immunocompromised close contacts. ( 5.2)

    ADVERSE REACTIONS

    The most common adverse reactions (incidence > 3%) were tiredness (31%), headache (29%), abdominal pain (19%), nausea/vomiting (18%), lack of appetite (17%) and diarrhea (4%). (6)

    To report SUSPECTED ADVERSE REACTIONS, contact PaxVax, Inc. at 1-800-533-5899 or safety@paxvax.com, or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.

    DRUG INTERACTIONS

    Avoid concomitant administration of VAXCHORA with systemic antibiotics since these agents may be active against the vaccine strain. Do not administer VAXCHORA to patients who have received oral or parenteral antibiotics within 14 days prior to vaccination. (7.2)

    Immune responses to VAXCHORA may be diminished when VAXCHORA is administered concomitantly with chloroquine. Administer VAXCHORA at least 10 days before beginning antimalarial prophylaxis with chloroquine. (7.2)

    USE IN SPECIFIC POPULATIONS

    Pregnancy Registry: available at 1-800-533-5899. (8.1)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 6/2016

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  • FULL PRESCRIBING INFORMATION: CONTENTS*
  • 1 INDICATIONS AND USAGE

    VAXCHORA is a vaccine indicated for active immunization against disease caused by Vibrio cholerae serogroup O1 in adults 18 through 64 years of age traveling to cholera-affected areas.

    1.1 Limitations of Use

    The effectiveness of VAXCHORA has not been established in persons living in cholera-affected areas.

    The effectiveness of VAXCHORA has not been established in persons who have pre-existing immunity due to previous exposure to V. cholerae or receipt of a cholera vaccine.

    VAXCHORA has not been shown to protect against disease caused by V. cholerae serogroup O139 or other non-O1 serogroups.

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  • 2 DOSAGE AND ADMINISTRATION

    For oral administration only.

    2.1 Dosage and Schedule

    Administer a single oral dose of VAXCHORA a minimum of 10 days before potential exposure to cholera.

    The safety and effectiveness of revaccination with VAXCHORA have not been established.

    2.2 Restrictions on Eating and Drinking

    Instruct recipients to avoid eating or drinking for 60 minutes before or after oral ingestion of VAXCHORA.

    2.3 Preparation, Reconstitution and Administration

    Prepare and administer VAXCHORA in a healthcare setting equipped to dispose of medical waste [see Disposal Instructions (2.4)].

    1.
    Reconstitution should be completed within 15 minutes of removing the carton from the freezer [see Storage and Handling (16.2)]. Locate the 2 packets: the buffer component (Packet 1) and the active component (Packet 2).
    2.
    Pour 100 mL of cold or room temperature (41°F-72°F; 5°C-22°C) purified bottled water into a clean, disposable cup. Do not use tap water, non-purified bottled water, other beverages, or other liquids.
    3.
    Use scissors to cut the top off the buffer component packet.
    4.
    Empty buffer component packet contents into cup. Effervescence will occur.
    5.
    Using a disposable stirrer, stir until the buffer component completely dissolves.
    6.
    Use scissors to cut the top off the active component packet.
    7.
    Empty the active component packet contents (lyophilized V. cholerae CVD 103-HgR) into the cup containing the buffer solution.
    8.
    Stir for at least 30 seconds and until active component disperses to form a slightly cloudy suspension that may contain some white particulates. The active component may not dissolve completely.
    9.
    VAXCHORA must be consumed within 15 minutes of reconstitution. The recipient should drink the full contents of the cup at once. Some residue may remain in the cup and should be discarded with the cup.

    NOTE: If the packets are reconstituted in the improper order, the vaccine must be discarded [see Disposal Instructions (2.4)].

    image of the prep, reconstitution and administration of Vaxchora

    2.4 Disposal Instructions

    Dispose of the cup, packets and stirrer according to standard procedures for medical waste.

    Inactivate any spilled vaccine and clean any non-disposable equipment used in the preparation of VAXCHORA with 70% isopropyl alcohol or 10% bleach solution.

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  • 3 DOSAGE FORMS AND STRENGTHS

    VAXCHORA is a suspension for oral administration. Before reconstitution, each dose of VAXCHORA is supplied as a foil packet of buffer and an accompanying foil packet of the active component (lyophilized V. cholerae CVD 103-HgR). After reconstitution, a single dose of VAXCHORA is 100 milliliters (mL).

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  • 4 CONTRAINDICATIONS

    Do not use in persons who have a history of severe allergic reaction (e.g., anaphylaxis) to any ingredient of VAXCHORA or to a previous dose of any cholera vaccine [see Description (11)].

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  • 5 WARNINGS AND PRECAUTIONS

    5.1 Altered Immunocompetence

    The safety and effectiveness of VAXCHORA have not been established in immunocompromised persons [see Immunocompromised Individuals (8.6)].

    5.2 Shedding and Transmission

    VAXCHORA may be shed in the stool of recipients for at least 7 days. There is a potential for transmission of the vaccine strain to non-vaccinated close contacts (e.g., household contacts) [see Pharmacodynamics (12.2)]. Use caution when considering whether to administer VAXCHORA to individuals with immunocompromised close contacts.

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  • 6 ADVERSE REACTIONS

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of a vaccine cannot be directly compared to rates in the clinical trials of another vaccine and may not reflect the rates observed in practice.

    The safety of VAXCHORA was evaluated in four randomized, placebo-controlled, multicenter clinical trials. A total of 3235 adults 18 through 64 years of age received one dose of VAXCHORA and 562 received placebo [physiologic saline (N=551) or lactose (N=11)]. Overall, the mean age was 32.5 years; 53.8% of trial participants were female; 67.1% were White, 27.3% were Black or African American, 1.8% were Asian, 1.7% were multiracial, 1.3% were other, 0.6% were American Indian or Alaskan Native and 0.3% were Native Hawaiian or Pacific Islander. There were 9.3% Hispanic or Latino participants.

    Solicited Adverse Reactions

    Adults 18 through 45 years of age received VAXCHORA in a multi-center, double-blind, randomized (8:1), placebo-controlled trial conducted in the United States and Australia (Study 1). The safety analysis set included 2789 VAXCHORA recipients. Solicited adverse reactions were recorded daily for 7 days following vaccination. Table 1 presents the frequency and severity of solicited adverse reactions observed within 7 days following receipt of VAXCHORA or placebo in Study 1.

    Table 1: Rates of Solicited Adverse Reactions Reported in VAXCHORA Trial Participants 18 to 45 Years of Age During 7 Days Post-Vaccination

    Study 1*
    VAXCHORA Placebo (Saline)
      Adverse Reaction (N=2789) (N=350)
    % %
    *
    Data are derived from Study 1 (NCT02094586).
    N represents number of subjects who completed a memory aid.
    Severe category includes both grade 3 (severe) and grade 4 (potentially life-threatening) adverse events.

      Tiredness

    31.3

    27.4

         Mild

    18.7

    16.3

         Moderate

    12.0

    9.9

         Severe

    0.7

    1.2

      Headache

    28.9

    23.6

         Mild

    18.9

    14.6

         Moderate

    9.6

    8.8

         Severe

    0.5

    0.3

      Abdominal Pain

    18.7

    16.9

         Mild

    12.1

    12.0

         Moderate

    6.2

    5.0

         Severe

    0.4

    0.0

      Nausea/Vomiting

    18.3

    15.2

         Mild

    13.3

    11.4

         Moderate

    4.7

    3.8

         Severe

    0.3

    0.0

      Lack of Appetite

    16.5

    16.6

         Mild

    11.7

    12.2

         Moderate

    4.4

    4.4

         Severe

    0.3

    0.0

      Diarrhea

    3.9

    1.2

         Mild

    2.4

    0.9

         Moderate

    0.7

    0.3

         Severe

    0.84

    0.0

      Fever

    0.6

    1.2

         Mild

    0.2

    0.3

         Moderate

    0.3

    0.9

         Severe

    0.11

    0.0

    Grading scales are defined as follows:

    Tiredness, Headache, Abdominal Pain, Nausea, Lack of Appetite: Mild = no interference with activity, Moderate = Some interference with activity, Severe = significant, prevents daily activity, Potentially Life Threatening = emergency room (ER) visit or hospitalization.

    Vomiting: Mild = 1-2 episodes/24 hours, Moderate = >2 episodes/24 hours, Severe = requires intravenous hydration, Potentially Life Threatening = ER visit or hospitalization for hypotensive shock.

    Diarrhea: Mild = 4 loose stools/24 hours, Moderate = 5 loose stools/24 hours, Severe = ≥6 loose stools /24 hours, Potentially Life Threatening = ER visit or hospitalization.

    Fever: Mild = 38.0-38.4°C/100.4-101.1°F, Moderate = 38.5-38.9°C/101.2- 102.0°F, Severe = 39.0-40.0°C/102.1-104.0°F, Potentially Life Threatening = >40.0 °C/104.0 °F.

    Serious Adverse Events

    In a pooled analysis of the four clinical studies, 0.6% (20/3235) of VAXCHORA recipients and 0.5% (3/562) of placebo recipients reported a serious adverse event within 6 months post-vaccination. None of these events were considered to be related to vaccination.

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  • 7 DRUG INTERACTIONS

    7.1 Food and Drink

    Avoid food or drink for 60 minutes before and after vaccine administration [see Restrictions on Eating and Drinking (2.2)].

    7.2 Concomitant Vaccines or Medications

    Vaccines

    No data are available on concomitant administration of VAXCHORA with other vaccines.

    Antibiotics

    Avoid concomitant administration of VAXCHORA with systemic antibiotics since these agents may be active against the vaccine strain and prevent a sufficient degree of multiplication to occur in order to induce a protective immune response. Do not administer VAXCHORA to patients who have received oral or parenteral antibiotics within 14 days prior to vaccination.

    Antimalarial Prophylaxis

    Data from a study with a similar product indicate that the immune responses to VAXCHORA may be diminished when VAXCHORA is administered concomitantly with chloroquine. Administer VAXCHORA at least 10 days before beginning antimalarial prophylaxis with chloroquine.

    7.3 Immunosuppressive Treatments

    Immunosuppressive therapies, including irradiation, antimetabolites, alkylating agents, cytotoxic drugs and corticosteroids (used in greater than physiologic doses), may reduce the immune response to VAXCHORA [see Use in Specific Populations (8.6)].

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  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Exposure Registry

    There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to VAXCHORA during pregnancy. To enroll in or obtain information about the registry, please call PaxVax at 1-800-533-5899.

    Risk Summary

    VAXCHORA is not absorbed systemically following oral administration, and maternal use is not expected to result in fetal exposure to the drug.

    Clinical Considerations

    Disease-associated maternal and/or embryo/fetal risk

    Maternal cholera disease is associated with adverse pregnancy outcomes including fetal death.

    Fetal/neonatal adverse reactions

    The vaccine strain may be shed in the stool of the vaccinated mother for at least 7 days, with a potential for transmission of the vaccine strain from mother to infant during vaginal delivery.

    8.2 Lactation

    Risk Summary

    VAXCHORA is not absorbed systemically by the mother following oral administration, and breastfeeding is not expected to result in exposure of the child to VAXCHORA.

    8.4 Pediatric Use

    The safety and effectiveness of VAXCHORA have not been established in children and adolescents younger than 18 years.

    8.5 Geriatric Use

    The safety and effectiveness of VAXCHORA have not been established in adults 65 years of age or older.

    8.6 Immunocompromised Individuals

    The safety and effectiveness of VAXCHORA have not been established in immunocompromised individuals. The immunologic response to VAXCHORA may be diminished in immunocompromised individuals [see Drug Interactions (7.3)].

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  • 11 DESCRIPTION

    VAXCHORA (Cholera Vaccine, Live, Oral) is a live, attenuated bacterial vaccine suspension for oral administration containing the V. cholerae strain CVD 103-HgR. CVD 103-HgR was constructed from the serogroup O1 classical Inaba strain 569B by deleting the catalytic domain sequence of both copies of the ctxA gene, which prevents the synthesis of active cholera toxin (CT). This attenuated strain remains able to synthesize the immunogenic non-toxic B subunit of CT (encoded by the ctxB gene). In addition, a marker was inserted into the hemolysin gene locus (hlyA) to enable differentiation of the vaccine strain from wild type V. cholerae O1.

    The vaccine strain is grown in fermentors under controlled conditions in medium containing casamino acids, yeast extract, mineral salts, and an anti-foaming agent. The bacteria are collected by filtration, diafiltered, and concentrated before addition of a stabilization solution containing ascorbic acid (an antioxidant), Hy-Case SF (hydrolyzed casein [a protein derived from cow's milk], a cryoprotectant), sodium chloride (a stabilizer), and sucrose (a cryoprotectant). The stabilized bacteria are lyophilized, milled, and blended with dried lactose (a desiccant and bulking agent). The active component blend is filled into packets.

    The buffer component is manufactured by blending together sodium bicarbonate (a gastric acid neutralizer), sodium carbonate (a buffer), ascorbic acid (a buffer and water chlorine neutralizer), and dried lactose (a manufacturing flow aid). The buffer component blend is filled into packets. One buffer component packet and one active component packet are packaged into individual single dose cartons for distribution.

    After reconstitution, VAXCHORA contains 4 x 108 to 2 x 109 colony forming units (CFU) of live attenuated V. cholerae CVD 103-HgR. The resulting suspension should be slightly cloudy and may contain white particulates. The active and buffer ingredients are shown in Table 2.

    Table 2: Vaccine Composition

    *
    CFU=colony forming units.
    mg=milligrams.
    g=grams.

    Ingredient

    Quantity/packet

    Active Component Packet

      V. cholerae CVD 103-HgR

    4 x 108 to 2 x 109 CFU*

      Sucrose

    ≤165.37 mg

      Sodium chloride

    ≤17.11 mg

      Hy-Case SF (hydrolyzed casein)

    ≤17.11 mg

      Ascorbic acid

    ≤8.55 mg

      Dried lactose

    ≤2.09 g

    Buffer Component Packet

      Sodium bicarbonate

    2.16-2.41 g

      Sodium carbonate

    0.24-0.49 g

      Ascorbic acid

    1.50-1.80 g

      Dried lactose

    0.18-0.22 g

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  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    VAXCHORA contains live attenuated cholera bacteria that replicate in the gastrointestinal tract of the recipient. Immune mechanisms conferring protection against cholera following receipt of VAXCHORA have not been determined. However, rises in serum vibriocidal antibody 10 days after vaccination with VAXCHORA were associated with protection in a human challenge study (Study 2) [See Immunogenicity (14.2)].

    12.2 Pharmacodynamics

    Shedding of the vaccine strain was evaluated in the first 7 days post-vaccination in a study of 53 healthy adult vaccine recipients (Study 3). VAXCHORA was shed in the stools of 11.3% [95% CI 4.3%, 23.0%] of vaccine recipients on any day through 7 days post-vaccination. During the 7 days post-vaccination, the proportion of subjects shedding was highest on day 7 (7.5% [95% CI 2.1%, 18.2%]). The duration of shedding of the vaccine strain is unknown.

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  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    VAXCHORA has not been evaluated for the potential to cause carcinogenicity or genotoxicity, or to impair fertility.

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  • 14 CLINICAL STUDIES

    14.1 Efficacy Against V. cholerae Challenge

    Study 2 was a randomized, double-blind, saline placebo-controlled V. cholerae challenge study conducted in the US. Subjects 18 through 45 years of age (N=197) with no prior history of cholera infection or travel to a cholera-endemic area in the previous 5 years were randomized according to a 1:1 ratio to receive one dose of VAXCHORA or placebo. In order to identify the subset of subjects to be challenged, an unblinded statistician prepared four randomly ordered lists of subjects per site, one list each for vaccine recipients with blood type O, vaccine recipients with non-O blood types, placebo recipients with blood type O, and placebo recipients with non-O blood types. This was done to maintain a minimum of 60% blood group O subjects in each treatment group. Individuals with type O blood are less likely to be infected with V. cholerae, but are at risk for developing severe cholera if infected. Each site was provided with a blinded version of the four lists specific to its site and advised on the number of subjects from each list to challenge. In the event that a subject was determined to be ineligible for challenge, the site was instructed to select the next subject from the same list as the ineligible subject

    The challenges were split into 2 cohorts for 10 day and 3 month challenges. Subjects were admitted to an inpatient unit. Subjects had nothing by mouth from midnight before ingestion of the challenge strain, except for water, and had nothing by mouth for 90 minutes after ingestion of the challenge strain. Approximately 1 minute prior to challenge, subjects ingested 120 mL sodium bicarbonate (NaHCO3) buffer. The oral challenge consisted of 1 x 105 CFU live wild type V. cholerae El Tor Inaba N16961 in 30 mL NaHCO3 buffer at 10 days or 3 months post-vaccination. The co-primary objectives were to demonstrate the efficacy of a single dose of VAXCHORA in the prevention of moderate to severe diarrhea following challenge at 10 days and 3 months post-vaccination. Moderate to severe diarrhea was defined as cumulative diarrheal purge ≥ 3 liters (L) within 10 days after challenge. Diarrheal stool was defined as ≥ 2 unformed stools (takes shape of container) collected during a 48 hour period ≥ 200 grams (g) or a single unformed stool ≥ 300 g. Subjects were instructed to collect every stool from the time of challenge until discharge from the inpatient unit. Nursing staff or study personnel inspected all stool, graded the consistency of the stool and calculated the total weight of diarrheal stool per day. Weight of stool was converted to volume using the formula 1 g=1 mL. VAXCHORA recipients challenged at 10 days post-vaccination and VAXCHORA recipients challenged at 3 months post-vaccination were compared with a pooled group of placebo (saline) recipients challenged at 10 days or 3 months post-vaccination.

    Of the 95 VAXCHORA recipients, 68 were challenged; 35 were challenged at 10 days post- vaccination and 33 were challenged at 3 months post-vaccination. Of the 102 placebo recipients, 66 were challenged; 33 were challenged at 10 days post-vaccination and 33 at 3 months post- vaccination. Among all randomized subjects, the mean age was 31.0 years. Overall, the mean age of the challenge population was 31.4 years. More males were in the vaccine group (71.6%) compared to the placebo group (54.9%). The majority of randomized subjects were Black (67.5%), 29.4% were White, 0.5% were American Indian/Alaskan Native, 0.5% were Asian, and 2.0% were other. There were 4.6% Hispanic or Latino participants. Overall 50.3% had blood type O. Among subjects selected for either challenge cohort, more males were challenged in the vaccine group (76.5%) compared to the placebo group (57.6%). The majority (70.9%) of the challenge population were Black, 25.4% were White, 0.7% were American Indian/Alaskan Native, 0.7% were Asian, and 2.2% were other. There were 3.7% Hispanic or Latino participants. Overall, 56.0% of challenged subjects had blood type O.

    Vaccine efficacy against the occurrence of moderate to severe diarrhea at 10 days post-vaccination was 90.3% [95% CI 62.7%, 100.0%] and at 3 months post-vaccination was 79.5% [95% CI 49.9%, 100.0%] (Table 3).

    Table 3: Vaccine Efficacy in the Prevention of Moderate to Severe Diarrhea Following Challenge with V. cholerae O1 El Tor Inaba at 10 Days and 3 Months Post-Vaccination (Intent-to-Treat Population)

    Combined Placebo*
    VAXCHORA VAXCHORA 10 Day or 3 Month
    10 Day Challenge* 3 Month Challenge* Challenge
      Parameter N=35§ N=33§ N=66§
    *
    Data are derived from Study 2 (NCT01895855).
    Combined placebo group comprised of all placebo recipients who were challenged at either 10 days (N=33) or 3 months (N=33) following vaccination.
    Challenge strain was V. cholerae O1 El Tor Inaba N16961.
    §
    N=number of subjects challenged in each group.
    Moderate or severe diarrhea (≥ 3 liters of diarrhea) within 10 days after challenge.
    #
    Vaccine Efficacy=[(Attack Rate in Placebo Group - Attack Rate in Vaccine Group)/Attack Rate in Placebo Group] x 100.
    Þ
    Pre-specified criteria for success were that the lower bound of the two-sided 95% confidence interval for vaccine efficacy must be ≥30% in both the 10 Day and 3 Month challenge groups.
    ß
    CI=confidence interval.

      Number of Subjects with

    2 (5.7%)

    4 (12.1%)

    39 (59.1%)

      Moderate or Severe

      Diarrhea (Attack Rate)

      

      Vaccine Efficacy %#Þ

    90.3%

    79.5%

      [95% CIß]

    [62.7%, 100.0%]

    [49.9%, 100.0%]

    14.2 Immunogenicity

    Vibriocidal Antibody Against the Vaccine Strain (classical Inaba)

    A vibriocidal antibody assay was used to measure serum levels of neutralizing antibodies against the vaccine strain.

    Study 2 was a randomized, double-blind, saline placebo-controlled V. cholerae challenge study conducted in adults 18 through 45 years of age. In the subset of subjects challenged in Study 2, 91% [95% CI 82%, 97%] of vaccinees seroconverted prior to challenge and 9% developed moderate to severe cholera following challenge, while 2% of placebo recipients seroconverted prior to challenge and 59% developed moderate to severe cholera following challenge. (Seroconversion was defined as a ≥ 4-fold rise in serum vibriocidal antibody from baseline to 10 days post-vaccination.) Based on the observed association between seroconversion and protection from V. cholerae disease, seroconversion rate at 10 days post-vaccination was used to evaluate response to vaccination in other age groups.

    Study 1 was a randomized, double-blind, saline placebo-controlled safety and immunogenicity study conducted in the US and Australia. A total of 3146 subjects 18 through 45 years of age not previously exposed to cholera were randomized 8:1 to receive one dose of VAXCHORA or placebo. The mean age was 29.9 years; 45.2% were male; 68.3% were White, 25.6% were Black, 2.0% were Asian, 1.9% were multiracial, 1.4% were other, 0.4% were American Indian/Alaskan Native, and 0.3% were Native Hawaiian/Pacific Islander. There were 10.0% Hispanic or Latino participants.

    In this study, the rates of seroconversion were 93.5% [95% CI 92.5%, 94.4%] in vaccine recipients and 4% [95% CI 2%, 7%] in placebo recipients at 10 days post-vaccination.

    Study 4 was a randomized, double-blind, placebo-controlled safety and immunogenicity study conducted in the US. A total of 398 subjects 46 through 64 years of age with no prior history of cholera infection or travel to a cholera-endemic area in the previous 5 years were randomized 3:1 to receive one dose of VAXCHORA or placebo. Overall, the mean age of the randomized population was 53.8 years; 45.7% were male; 74.9% were White, 21.9% were Black, 1.8% were American Indian/Alaskan Native, 0.5% were Asian, 0.5% were multiracial, 0.3% were Native Hawaiian/Pacific Islander, and 0.3% were other. There were 7.5% Hispanic or Latino participants.

    Seroconversion rates at 10 days post-vaccination by classical Inaba vibriocidal antibody among 46 through 64 year old subjects in Study 4 were compared to those in 18 through 45 year old subjects in Study 1. VAXCHORA recipients from Study 1 were in the same age group as those in Study 2, the V. cholerae challenge study.

    Adults 46 through 64 years were shown to have a non-inferior rate of seroconversion by classical Inaba vibriocidal antibody at 10 days post-vaccination compared to adults 18 through 45 years of age (Table 4).

    Table 4: Vibriocidal Antibody Seroconversion Against Classical Inaba V. cholerae Vaccine Strain at 10 Days Post-Vaccination in Adults 46 through 64 Years of Age (Study 4) Compared to Adults 18 through 45 Years of Age (Study 1) [Bridging Analysis Population]

    VAXCHORA
    Seroconversion
    VAXCHORA %
    Study* Dose/CFU N [95% CI]
    *
    Data are derived from Study 1 (NCT02094586) and Study 4 (NCT02100631).
    N=number of subjects with analyzable samples at Day 1 and Day 11.
    CI=confidence interval.
    §
    Seroconversion is defined as the percentages of subjects who had at least a 4-fold rise in vibriocidal antibody titer at 10 days post-vaccination compared to baseline.
    Pre-specified non-inferiority criterion was that the lower bound of the two-sided 95% confidence interval on the difference in seroconversion rate (Study 4 minus Study 1) must be greater than -10 percentage points.

    Study 4
    (46 through 64 year olds)

    1 x 109

    291

    90.4%
    [86.4%, 93.5%]

      

    Study 1
    (18 through 45 year olds)

    1 x 109

    2687

    93.5%
    [92.5%, 94.4%]

      

    Difference in Seroconversion
    Rates§

    -3.1%
    [-6.7%, 0.4%]

    Vibriocidal Antibody Against Classical Ogawa, El Tor Inaba and El Tor Ogawa

    V. cholerae serogroup O1 consists of four major subtypes: classical Inaba, classical Ogawa, El Tor Inaba and El Tor Ogawa. Serum vibriocidal antibody against the three types of V. cholerae not contained in the vaccine, namely classical Ogawa, El Tor Inaba and El Tor Ogawa, was also measured in Study 2 and Study 4. The percentages of vaccine recipients who seroconverted against each of the 4 major biotype/serotypes of V. cholerae serogroup O1 at 10 days post- vaccination (71.4% to 91.4%) are shown in Table 5.

    Table 5: Seroconversion Rates 10 Days Post-Vaccination for the Four Major V. cholerae O1 Serogroup Biotypes and Serotypes in Studies 2 and 4 [Immunogenicity Evaluable Population]

    Study 2*
    (18 through 45 year olds)
    VAXCHORA
    Study 4*
    (46 through 64 year olds)
    VAXCHORA
    Cholera Strain N %
    [95% CI§]
    N %
    [95% CI]
    *
    Data are derived from Study 2 (NCT01895855) and Study 4 (NCT02100631).
    N=number of subjects with measurements at baseline and 10 days post-vaccination. One subject in Study 2 did not have a Day 11 measurement and was dropped from the analysis.
    Seroconversion is defined as the percentages of subjects who had at least a 4-fold rise in vibriocidal antibody titer at 10 days post-vaccination compared to the titer measured at baseline.
    §
    CI=confidence interval.
    VAXCHORA contains the classical Inaba strain of V. cholerae O1.

      Classical Inaba

    93

    90.3%
    [82.4%, 95.5%]

    291

    90.4%
    [86.4%, 93.5%]

      El Tor Inaba

    93

    91.4%
    [83.8%, 96.2%]

    290

    91.0%
    [87.1%, 94.1%]

      Classical Ogawa

    93

    87.1%
    [78.5%, 93.2%]

    291

    73.2%
    [67.7%, 78.2%]

      El Tor Ogawa

    93

    89.2%
    [81.1%, 94.7%]

    290

    71.4%
    [65.8%, 76.5%]

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  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    VAXCHORA is supplied as shown in Table 6. The contents of both packets are reconstituted with purified bottled water, to form one oral dose of the vaccine.

    Table 6: VAXCHORA Product Presentation
      Presentation   Carton NDC Number   Components

      Single dose carton containing two

      NDC 70460-001-01

      Buffer Component Packet NDC 70460-003-02

      packets

      Active Component Packet NDC 70460-002-02

    16.2 Storage and Handling

    Store VAXCHORA buffer component and active component packets frozen at -13°F to 5°F (-25°C to -15°C).

    Protect from light and moisture.

    Packets do not require thawing prior to reconstitution. Packets should not be out of frozen storage for more than 15 minutes prior to reconstitution; when out of frozen storage, packets should not be exposed to temperatures above 80°F (27°C).

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  • 17 PATIENT COUNSELING INFORMATION

    Prior to administration of this vaccine, the health care professional should inform the individual of the following:

    Advise vaccine recipients to exercise caution regarding food and water consumed in cholera-affected areas, in accordance with the recommendations from the Centers for Disease Control and Prevention for the prevention of cholera in travelers.
    Educate vaccine recipients regarding the most common adverse reactions occurring within 7 days post-vaccination with VAXCHORA (tiredness, headache, abdominal pain, nausea/vomiting, lack of appetite, and diarrhea).
    Inform vaccine recipients that VAXCHORA is a live attenuated vaccine and has the potential for transmission of the vaccine strain to close contacts (e.g., household contacts). For at least 14 days following vaccination with VAXCHORA, vaccine recipients should wash their hands thoroughly after using the bathroom and before preparing or handling food.
    Register women who receive VAXCHORA while pregnant in the pregnancy registry by calling 1-800-533-5899 [see Pregnancy (8.1)].
    Instruct vaccine recipients to report adverse reactions to their healthcare provider.

    VAXCHORA is a trademark of PaxVax Bermuda Ltd.
    US License No. 2041
    Manufactured by: PaxVax Bermuda Ltd.

    Distributed by: PaxVax, Inc., 900 Veterans Blvd., Suite 500, Redwood City, CA 94063, USA

    Version: June 2016
    © 2016 PaxVax. All rights reserved.

    Art. No. DSN 102

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  • PRINCIPAL DISPLAY PANEL


    Package Label - CARTON - Cholera Vaccine, Live, Oral Vaxchora

    PRINCIPAL DISPLAY PANEL

    NDC 70460-001-01    

    STORE FROZEN
    Use After Reconstitution

    Cholera Vaccine, Live, Oral
    Vaxchora

    Contents: Single-dose Active Packet (4x108 to 2x109 CFU of
    V. cholerae CVD 103-HgR) and Single-dose Buffer Packet.

    Prior to administration, reconstitute Buffer in 100 mL of purified
    bottled water, then add Active. See package insert.

    PaxVax

    carton - Cholera Vaccine, Live, Oral Vaxchora
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  • INGREDIENTS AND APPEARANCE
    VAXCHORA 
    cholera vaccine, live, oral kit
    Product Information
    Product Type VACCINE Item Code (Source) NDC:70460-001
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70460-001-01 1 in 1 CARTON; Type 0: Not a Combination Product
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 PACKET
    Part 2 1 PACKET
    Part 1 of 2
    VAXCHORA 
    cholera vaccine, live, oral powder, for suspension
    Product Information
    Item Code (Source) NDC:70460-002
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN (UNII: V9G528E9E0) (VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN - UNII:V9G528E9E0) VIBRIO CHOLERAE CVD 103-HGR STRAIN LIVE ANTIGEN 1200000000 [CFU]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROLYZED CASEIN (ENZYMATIC; 1000 MW) (UNII: M93H91U80R)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70460-002-02 1 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA125597 10/03/2016
    Part 2 of 2
    BUFFER 
    buffer powder, for suspension
    Product Information
    Item Code (Source) NDC:70460-003
    Route of Administration ORAL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70460-003-02 1 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA125597 10/03/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA125597 10/03/2016
    Labeler - Paxvax, Inc. (080128378)
    Registrant - Paxvax, Inc. (080128378)
    Establishment
    Name Address ID/FEI Business Operations
    Paxvax, Inc. 080128378 LABEL(70460-001) , API MANUFACTURE(70460-002) , MANUFACTURE(70460-001)
    Establishment
    Name Address ID/FEI Business Operations
    Alliance Contract Pharma, Llc 831390914 MANUFACTURE(70460-003) , ANALYSIS(70460-003)
    Establishment
    Name Address ID/FEI Business Operations
    Bioconvergence Llc 620582002 LABEL(70460-001) , PACK(70460-001)
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