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A Phase 2 Safety and Immunogenicity Study for an Anthrax Vaccine Using 3 Schedules and Two Dose Levels

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Emergent BioSolutions
ClinicalTrials.gov Identifier:
NCT01770743
First received: January 16, 2013
Last updated: October 24, 2014
Last verified: October 2014
  Purpose

The purpose of this study is to assess the safety and immunogenicity of an anthrax vaccine. The vaccine schedule and dose will also be assessed.


Condition Intervention Phase
Anthrax
Biological: AV7909
Biological: BioThrax
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Phase 2, Randomized, Parallel-Group, Active-Controlled, Double-Blind Study to Evaluate the Safety and Immunogenicity of AV7909 for Post-Exposure Prophylaxis of Anthrax Using Three Immunization Schedules and Two Dose Levels in Healthy Adult Volunteers

Resource links provided by NLM:


Further study details as provided by Emergent BioSolutions:

Primary Outcome Measures:
  • Toxin Neutralizing Antibody (TNA) Level at Day 63 [ Time Frame: Day 63 ] [ Designated as safety issue: No ]
    Immunogenicity measured by the lower bound (LB) of the 95% confidence intervals (CIs) for the proportion of subjects in each study arm with Day 63 TNA 50% neutralization factor (NF50) values greater than or equal to threshold

  • Number of Adverse Events [ Time Frame: Up to 12 months ] [ Designated as safety issue: Yes ]
    Safety will be evaluated by adverse events, including assessment of symptoms, physical exam findings, clinical laboratory tests, and vital signs.


Secondary Outcome Measures:
  • TNA Level at Day 42 [ Time Frame: Day 42 ] [ Designated as safety issue: No ]
    Immunogenicity measured by the percentage of subjects in each study arm with Day 42 TNA NF50 values greater than or equal to threshold

  • TNA Level at Day 28 [ Time Frame: Day 28 ] [ Designated as safety issue: No ]
    Immunogenicity measured by the percentage of subjects with Day 28 TNA NF50 values greater than or equal to threshold

  • TNA Seroconversion Rate [ Time Frame: Up to Day 84 ] [ Designated as safety issue: No ]
    Immunogenicity measured by the percentage of subjects who have seroconverted (defined as a 4-fold increase over Day 0 in TNA NF50 value) at Days 21, 28, 35, 42, 49, 63, and 84


Estimated Enrollment: 168
Study Start Date: January 2013
Estimated Study Completion Date: December 2014
Primary Completion Date: February 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: AV7909 (Day 0 and 14)
Route of administration: Intramuscular Dose: 0.5 mL Schedule: Day 0 and Day 14
Biological: AV7909
Anthrax Vaccine Adsorbed plus CPG 7909 Adjuvant
Other Names:
  • AV7909 Anthrax Vaccine
  • NuThrax
Experimental: AV7909 (Day 0 and 28)
Route of administration: Intramuscular Dose: 0.5 mL Schedule: Day 0 and Day 28
Biological: AV7909
Anthrax Vaccine Adsorbed plus CPG 7909 Adjuvant
Other Names:
  • AV7909 Anthrax Vaccine
  • NuThrax
Experimental: AV7909 (Day 0, 14, and 28)
Route of administration: Intramuscular Dose: 0.5 mL Schedule: Day 0, Day 14,and Day 28
Biological: AV7909
Anthrax Vaccine Adsorbed plus CPG 7909 Adjuvant
Other Names:
  • AV7909 Anthrax Vaccine
  • NuThrax
Experimental: AV7909 Reduced Dose
Route of administration: Intramuscular Dose: 0.25 mL Schedule: Day 0, Day 14,and Day 28
Biological: AV7909
Anthrax Vaccine Adsorbed plus CPG 7909 Adjuvant
Other Names:
  • AV7909 Anthrax Vaccine
  • NuThrax
Active Comparator: BioThrax
Route of administration: Intramuscular Dose: 0.5 mL Schedule: Day 0, Day 14,and Day 28
Biological: BioThrax
Other Name: Anthrax Vaccine Adsorbed (AVA)

Detailed Description:

The safety and immunogenicity of AV7909 for post-exposure prophylaxis of anthrax will be evaluated using a randomized, parallel-group, active-controlled, double-blind design with three immunization schedules and two dose levels in healthy adult volunteers. Safety will be assessed by clinical laboratory tests (hematology, serum chemistry, and urinalysis), monitoring of adverse events, vital signs, and physical examinations. Reactogenicity (systemic and injection site reactions) will be assessed by the subjects using subject e-diaries for 7 days after each immunization and by the investigator at in-clinic visits 7 and 14 days after each immunization, and at other visits, if applicable. Immunogenicity will be measured as toxin neutralizing antibody (TNA) response and seroconversion rates.

  Eligibility

Ages Eligible for Study:   18 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Be 18-50 years old
  • Be in good health
  • Have access to a computer and the internet so you can complete a diary
  • Agree to abstain from sex the first 84 days of the study or practice birth control if you are a woman who is able to get pregnant
  • Have not donated blood for the previous 8 weeks

Exclusion Criteria:

  • A known anaphylactic response, severe systemic response, or serious hypersensitivity reaction to a prior immunization.
  • A history of latex allergy.
  • Have received a shot (vaccine), including flu shots, in the past 6 weeks or plan to get a shot for 4 weeks after the last study shot is given.
  • Have previously served in the military any time after 1990 or plan to enlist in the military from Screening through Day 84.
  • Prior immunization with anthrax vaccine, recombinant protective antigen (rPA) vaccine, or known exposure to anthrax organisms.
  • Have participated in anthrax therapeutic or vaccine studies (monoclonal anti-PA or anthrax immune globulins or anthrax vaccines).
  • Participation in any investigational study involving use of a pharmacological intervention within 30 days before the Screening visit or planning to participate in a study requiring dosing through the 12-month safety follow-up telephone call.
  • Have a known diagnosis of any immunodeficiency disease including but not limited to: acquired immune deficiency syndrome (AIDS), common variable immunodeficiency disease, immunoglobulin A (IgA) deficiency, or hypogammaglobulinemia.
  • Past history of significant autoimmune disease such as rheumatoid arthritis, lupus erythematous, psoriasis in the area of vaccinations, or requires immunotherapy, glomerulonephritis, or autoimmune thyroiditis.
  • Have received immunosuppressive therapy with cytotoxic drugs or Rituximab within the past 2 years.
  • A history of cytotoxic chemotherapy or radiation therapy.
  • Chronic (>10 days) daily oral or parenteral corticosteroid therapy in the past 12 months.
  • Any lung disease, including reactive airway disease, which requires the daily use of medications.
  • A female currently breastfeeding or with a positive pregnancy test.
  • A history of drug or alcohol abuse within 12 months prior to Screening, or a positive result on a urine drug screen for cocaine, marijuana, opiates, methamphetamines, benzodiazepines, or oxycodone.
  • Any tattoo or other skin condition in the deltoid region on either arm that may obscure the assessment of the injection sites.
  • A medical condition that, in the opinion of the PI or designee, could adversely impact the subject's participation or safety or the conduct of the study.
  • Any planned elective in-patient surgery during the study period.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01770743

Locations
United States, Florida
Miami Research Associates
Miami, Florida, United States, 33143
United States, South Carolina
Costal Carolina Research
Mount Pleasant, South Carolina, United States, 29464
United States, Texas
Central Texas Allergy and Asthma
New Braunfels, Texas, United States, 78130
United States, Utah
Jean Brown Research
Salt Lake City, Utah, United States, 84124
Sponsors and Collaborators
Emergent BioSolutions
Investigators
Principal Investigator: Gurdyal Kalsi, MD, MTOPRA Emergent BioSolutions
  More Information

No publications provided

Responsible Party: Emergent BioSolutions
ClinicalTrials.gov Identifier: NCT01770743     History of Changes
Other Study ID Numbers: EBS.AVA.208 / DMID 11-0055, HHSN272201000035C
Study First Received: January 16, 2013
Last Updated: October 24, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Emergent BioSolutions:
post-exposure prophylaxis
toxin neutralization assay

Additional relevant MeSH terms:
Anthrax
Bacillaceae Infections
Bacterial Infections
Gram-Positive Bacterial Infections

ClinicalTrials.gov processed this record on November 27, 2014