Phase 3, Randomized, Safety, Lot Consistency and Clinical Benefit Study of Recombinant Botulinum Vaccine A/B

NCT01940315 | Withdrawn Phase 3 DMC FDA Drug

• 1 other identifier: rBV A/B-03
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

This Phase 3 clinical trial is a double blind, placebo-controlled, randomized, multicenter investigation of rBV A/B in male and female healthy adults 18 to 55 years of age.

Conditions

Botulism

Keywords

Defender Study; experimental vaccine; inhalational intoxication

Outcome Measures

Primary Outcomes (2)

• The primary safety objective is to demonstrate the safety of rBV A/B through Day 365.

  The primary safety endpoints are the incidence, severity and relationship to treatment of solicited local, systemic and neuromuscular adverse events (AEs) with onset on the day of and for 7 days after each administration of study product; treatment-emergent AEs (TEAEs) with onset within 28 days after each administration of study product; and medically-attended AEs (MAEs), neuromuscular AEs and serious AEs (SAEs) from the time of first dose (Day 0) through 6 months after the last dose (Day 365).

  1 year after first dose [Dose 1] / 6 months after the last dose [Dose 3]

• The primary immunogenicity objectives are to demonstrate lot consistency for three lots of rBV A/B and to infer clinical benefit of rBV A/B.

  * The criterion to demonstrate lot consistency will be based on the geometric mean ratios of neutrailzing antibodies concentrations (NAC) to vaccine antigens BoNT/A1 and BoNT/B1. * The criterion to demonstrate clinical benefit is the proportion of volunteers with NAC values at or above the putative protective levels for anti-BoNT/A1 and anti-BoNT/B1 simultaneously.

  Study Day 210, approximately 28 days after the last dose [Dose 3]

Secondary Outcomes (2)

• The secondary safety objective is to demonstrate the safety of rBV A/B from Day 365 through Day 547.

  1 year after last dose [Dose 3] in a subset of volunteers

• The secondary immunogenicity endpoints is duration of protection through Day 547.

  Evalution through Study Days 365 and 547 (6 months and 1 year after last dose [Dose 3])

Study Arms (2)

rBV A/B

ACTIVE COMPARATOR

0.5 mL dose of rBV A/B (40 µg) will be administered intramuscularly (IM) in a three-dose dosing schedule given at Days 0, 28 ± 5 days, and 182 ± 9 days

Biological: rBV A/B

Placebo

PLACEBO COMPARATOR

0.5 mL dose of placebo will be administered intramuscularly (IM) given at Days 0, 28 ± 5 days, and 182 ± 9 days

Biological: Placebo (USP sterile saline for injection)

Interventions

rBV A/B BIOLOGICAL

0.5 mL dose of rBV A/B (40 µg) given at Days 0, 28 ± 5 days, and 182 ± 9 days

rBV A/B

Placebo (USP sterile saline for injection) BIOLOGICAL

0.5 mL dose of Placebo will be given at Days 0, 28 ± 5 days, and 182 ± 9 days

Placebo

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• The volunteer is a U.S. citizen or permanent resident alien of the U.S.
• The volunteer has signed the informed consent form.
• The volunteer is 18 to 55 years of age.
• The volunteer agrees not to donate blood or blood product for therapeutic or research purposes.
• The volunteer is willing to comply with the requirements of the protocol through the last scheduled visit.
• The volunteer is accessible by telephone or electronic mail to receive reminders from the investigative site.
• Female volunteers of childbearing potential must not be pregnant or lactating and agree to use two types of an acceptable form of FDA-approved contraception through end of study.
• The volunteer is in good health.
• The volunteer has clinical laboratory tests within acceptable ranges listed in the protocol.

You may not qualify if:

• The volunteer has a history of botulism or prior receipt of any botulinum vaccine, toxoid or antitoxin.
• The volunteer has previously been treated or expects to be treated with any therapeutic products containing BoNTs such as Botox®, Myobloc®/Neurobloc™ and Botox® Cosmetic.
• The volunteer has a history of hypersensitivity or significant adverse reaction to other vaccines, aluminum compounds or yeast.
• The volunteer has a history of severe allergic reactions or anaphylaxis.
• The volunteer has donated one or more units of blood (≥ 450 mL) or undergone plasmapheresis within the past 28 days prior to receiving first administration of study product.
• The volunteer received any blood product or immunoglobulin in the previous 6 months prior to receiving first vaccination or plans to receive such products during the clinical trial.
• The volunteer received any investigational vaccine in the previous 6 months.
• The volunteer received or intends to receive any licensed nonliving vaccine within 14 days before or after a scheduled administration of study product.
• The volunteer received or intends to receive any licensed live vaccine, including FluMist® within 60 days before or after a scheduled administration of study product.
• Vaccination with commercially available inactivated or non-living influenza vaccine preparations (other than FluMist®) if received 14 days before and after a scheduled administration of study product.
• The volunteer received any investigational drug therapy within 30 days before the first vaccination or before the last scheduled visit.
• The volunteer received therapy with immunosuppressive agents, including use of moderate to high-dose oral inhaled or systemic corticosteroids (prednisone-equivalent dose of ≥ 20 mg/day).
• The volunteer has or develops medically diagnosed chronic migraine headaches (persistent and recurrent) or a neurological condition associated with a cranial nerve or spasticity or abnormal muscle contraction, demyelination, other abnormalities of smooth or skeletal muscle function or hyperhidrosis.
• The volunteer had systemic or recurrent disease or condition that would place the volunteer at an unacceptable risk of injury or requires frequent or continuous medical intervention for treatment, has required hospitalization, or is likely to require surgical intervention during the course of the study.
• The volunteer has a history of immunodeficiency or autoimmune disease.

Sponsors & Collaborators

• DynPort Vaccine Company LLC, A GDIT Company: lead

MeSH Terms

Conditions

Botulism

Interventions

Injections

Condition Hierarchy (Ancestors)

Clostridium Infections; Gram-Positive Bacterial Infections; Bacterial Infections; Bacterial Infections and Mycoses; Infections; Neuromuscular Junction Diseases; Neuromuscular Diseases; Nervous System Diseases; Neurotoxicity Syndromes; Foodborne Diseases; Poisoning; Chemically-Induced Disorders

Intervention Hierarchy (Ancestors)

Drug Administration Routes; Drug Therapy; Therapeutics

Study Officials

• George A Saviolakis, M.D., Ph.D.

  DynPort Vaccine Company LLC, A GDIT Company

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 6, 2013
• First Posted: September 12, 2013
• Study Start: October 1, 2017
• Primary Completion: March 1, 2019
• Study Completion: September 1, 2019
• Last Updated: December 4, 2018

Record last verified: 2018-11