Title: Recombinant Plague Vaccine rF1V in Healthy Volunteers

Phase 2

Completed

• Conditions: Healthy Volunteers
• Interventions: Biological: rF1V vaccine; Biological: rFIV vaccine; Biological: rF1V vaccine 160 mcg given on Study Days 0, 56, 182

• Registration Number: NCT00332956
• Lead Sponsor: DynPort Vaccine Company LLC, A GDIT Company

Brief Summary

This Phase 2(a) clinical trial is designed as a dose-blinded, block-randomized, multi-center study to select a dosage and schedule of rF1V vaccine for further studies based on the immune response up to Day 210. Additional immunogenicity and safety/reactogenicity data will be collected through Day 540. Selection of dosage and schedule will be based on GMCs and seroconversion rates for anti-F1, anti-V and anti-rF1V antibody titers. Approximately 400 healthy adult volunteers will be enrolled (100 per group) in this study.

Detailed Description

Primary Objective: To select a dosage and schedule of rF1V vaccine for further study based on the immune response to F1 and V antigens up to Day 210.

Secondary Objectives: 1) To assess the safety of three injections of rF1V vaccine administered IM at two dosage levels.

2) To assess the onset and duration of the humoral immune response to F1 and V antigens.

3) To assess the humoral immune response to rF1V antigen. 4) To collect and store blood samples for future plague related research.

Exploratory Objectives:

To assess additional humoral immune responses to rF1V vaccine antigens.

Study Timeline

• Study Start: 2006-05
• Study First Submitted: 2006-06-01
• Study First Submitted QC: 2006-06-01
• Study First Posted: 2006-06-02
• Primary Completion: 2008-02
• Study Completion: 2008-10
• Disposition First Submitted: 2011-06-29
• Disposition First Submitted QC: 2011-06-29
• Disposition First Posted: 2011-07-01
• Status Verified: 2011-11
• Last Update Submitted: 2011-11-28
• Last Update Posted: 2011-12-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

1. Male or Female age 18 to 55 years
2. In good health
3. Acceptable ranges for the laboratory parameters
4. Normal ECG. If a volunteer is reported to have a benign ECG abnormality(e.g., sinus bradycardia) the results may be discussed with the medical monitors for the study.
5. Willing to have his/her blood samples stored for future plague research studies.
6. Signed the ICF and HIPPA and successfully completed the Test of Understanding (90% correct).
7. Agrees not to donate blood until at least 90 days following the last vaccination.
8. Volunteer is willing to comply with the requirements of the protocol through the post-vaccination Day 540 visit.
9. Female volunteers must be of non-childbearing potential or must not be pregnant. Must use 2 types of acceptable for of FDA approved contraception or abstinent.

Exclusion Criteria

1. A history of plague disease or have previously received any plague vaccine.
2. Active tuberculosis or other systemic infectious process.
3. History of allergy to kanamycin or other aminoglycosides (e.g., gentamicin, tobramycin, amikacin)
4. Positive prescreening for human immunodeficiency virus (HIV); hepatitis C virus (HCV) or hepatitis B surface antigen (HbsAg).
5. A history of immunodeficiency or chronic illness requiring continuous or frequent medical intervention, acute/chronic untreated conditions, autoimmune disease or use of immunosuppressive medications.
6. Chronic, severe or recurrent joint pain (4 or more occurrences per year) or arthritis of any type.
7. A positive result on a urine drug screen that tests for common substances of abuse such as amphetamines, barbiturates, benzodiazepines, cocaine, opiates and cannabinoids.
8. A previous diagnosis of any serious psychiatric disorder. For this purpose, serious psychiatric disorder is defined as illness requiring hospitalization within the previous 12 months; routine administration of more than one medication to control anxiety, mood or sleep disorder; or history of suicide attempt.
9. Receipt of any blood product or immune globulin in the previous 6 months.
10. Receipt of any investigational vaccine in the previous 6 months
11. Donation of blood within 56 days prior to first vaccination or at any time prior to Day 210 visit.
12. Receipt of any investigational drug therapy within 30 days before the first dose of rF1V or intent to receive any other investigational drug therapy before the post-vaccination Day 540 visit.
13. A clinically significant abnormality on the ECG.
14. A body mass index > or equal to 35 kg/m2
15. Acute illness, evidence of significant active infection or systemic disease at time of enrollment that in the opinion of the Investigator would place the volunteer at an unacceptable risk for injury.
16. Personal history of multiple sclerosis, since immune system stimulation may exacerbate this disorder.
17. Occupational or other responsibilities that would prevent completion of participation in the study.
18. Licensed vaccines are not exclusionary but should be given at least 2 weeks before or after immunization (if live vaccine, 60 days before or after immunization) to avoid potential confusion of adverse reactions.
19. Screening laboratory values not within acceptable ranges.
20. A history of anaphylaxis or other serious adverse reactions to vaccines.
21. The female volunteer is pregnant
22. Receipt of therapy with immunosuppressive agents, including high-dose systemic corticosteroids (i.e., prednisone-equivalent dose of > or equal to 20 mg/day), within 3 months prior to or during the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group 3	rF1V vaccine	Volunteers will be vaccinated with 160 mcg rF1V vaccine given on Study Days 0, 28, 182
Group 1	rFIV vaccine	Volunteers will be vaccinated with 80 mcg rF1V vaccine on Study Days 0 , 28, 182
Group 2	rF1V vaccine	Volunteers will be vaccinated with 80 mcg of rF1V vaccine at Study Days 0, 56, 182
Group 4	rF1V vaccine 160 mcg given on Study Days 0, 56, 182	Volunteers will be vaccinated with 160 mcg rf1V vaccine on Study Days 0, 56, 182

Primary Outcome Measures

Name	Time	Method
To select a final dosage and schedule of rF1V vaccine based on the immune response to F1 and V antigens up to Day 210	Day 210 Interim Analysis

Secondary Outcome Measures

Name	Time	Method
To access the safety of three injections of rF1V vaccine administered IM at two dosage levels.	Day 210 Interim Analysis
To access the onset and duration of the humoral immune response to F1 and V antigens	Final Clinical Study Reort
To assess the humoral immune response to rF1V antigen	Final Clinical Study Report
To collect and store blood samples for future plague related research.	Through Study Day 540

Trial Locations

Locations (9)

Infectious Disease Specialists, PC; 🇺🇸 Missoula, Montana, United States

Primary Physicians Research, Inc.; 🇺🇸 Pittsburgh, Pennsylvania, United States

University of Kentucky - Dept. of Infectious Disease; 🇺🇸 Lexington, Kentucky, United States

Palm Beach Research; 🇺🇸 West Palm Beach, Florida, United States

Sundance Clinical Research; 🇺🇸 St. Louis, Missouri, United States

Clinical Research Center of Nevada; 🇺🇸 Las Vegas, Nevada, United States

Benchmark Research; 🇺🇸 San Francisco, California, United States

Alta Clinical Research, LLC; 🇺🇸 Tucson, Arizona, United States

Meridian clinical Research, LLC; 🇺🇸 Omaha, Nebraska, United States