Safety and Immunogenicity of Q Fever Vaccine

NCT02092142 | Withdrawn Phase 2

• 2 other identifiers: S-11-19FY13-02
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate the safety of Q Fever Vaccine, Phase I, Inactivated, Dried, NDBR 105 and collect data on incidence of occupational Q fever infection in vaccinated personnel.

Conditions

Q Fever

Keywords

Q fever; Coxiella burnetii

Outcome Measures

Primary Outcomes (9)

• Change in Immunogenicity

  Immune response will be evaluated for per protocol subjects to determine the percentage of subjects who experience a ≥ fourfold rise in immunofluorescence assay (IFA) antibody titer after vaccination. Immunoglobulin M (IgM) at Day 28 or Day 56, or immunoglobulin G (IgG) at 6 months.

  Day 28, Day 56, or 6 months

• Percentage of subjects with symptoms following Q fever vaccination

  6 months

• Percentage of subjects with erythema following Q fever vaccination along with severity and association with vaccination

  6 months

• Percentage of subjects with induration following Q fever vaccination along with severity and association with vaccination

  6 months

• Percentage of subjects with each AE, system organ class of AE, severity, and association with vaccination

  6 months

• Percentage of subjects with symptoms following Q fever skin test antigen

  6 months

• Percentage of subjects with erythema following Q fever skin test antigen along with severity and association with skin test antigen

  6 months

• Percentage of subjects with induration following Q fever skin test antigen along with severity and association with skin test antigen

  6 months

• Percentage of subjects with each AE, system organ class of AE, severity, and association with skin test antigen

  6 months

Study Arms (1)

Vaccinated

EXPERIMENTAL

The vaccine will be administered subcutaneously in the upper outer aspect of the arm (triceps area) with 0.5 mL Q fever Vaccine, Phase I, Inactivated, Dried, NDBR 105 (which equals 30 μg)

Biological: Q fever Vaccine

Interventions

Q fever Vaccine BIOLOGICAL

Subcutaneous 0.5 mL Q fever Vaccine, Phase I, Inactivated, Dried, NDBR 105

Also known as: Q fever Vaccine, Phase I, Inactivated, Dried, NDBR 105

Vaccinated

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• At least 18 years old.
• Females of childbearing potential must agree to have a urine pregnancy test on the same day before receipt of skin test AND vaccine. (Exception: documented hysterectomy or ≥ 3 years of menopause.) The results must be negative. Females must agree to not become pregnant for 3 months after receipt of the skin test or vaccination.
• Considered at risk for exposure to C burnetii and who have submitted a Request for Investigational New Drug (IND) Vaccines for the Q Fever vaccine.
• Sign and date the approved informed consent document and Health Insurance Portability and Accountability Act (HIPAA) Authorization.
• Have on their charts:
• Up-to-date medical history (including concomitant medications)
• Physical examination and laboratory tests within 1 year
• Previous chest x-ray and electrocardiogram
• Be medically cleared for participation by an investigator. Examinations or tests may be repeated at the discretion of the enrolling physician.
• Willing to return for all follow-up visits.
• Agree to report any adverse events (AEs) that may or may not be associated with administration of the test article for at least 28 days after vaccination and agree to report all serious adverse events (for example, resulting in hospitalization) for the duration of the subject's participation in the study (6 months).
• Agree to defer blood, bone marrow, and organ donation for 1 year after receipt of skin test antigen and/or vaccine.

You may not qualify if:

• Prior history of Q fever disease or vaccination.
• Clinically significant abnormal lab results (including evidence of hepatitis C, hepatitis B carrier state) or elevated liver function tests (two times the normal range or at the discretion of the principal investigator).
• Personal history of an immunodeficiency or current treatment with an oral or intravenous immunosuppressive medication.
• Confirmed HIV infection.
• Heart valve disease: prosthetic heart valve or clinically significant heart murmur. (If a murmur is detected on examination, an echocardiogram may be obtained or subject may be referred to a cardiologist to determine clinical significance.)
• Aneurysm/vascular graft.
• Joint prosthesis.
• History of chronic fatigue syndrome (or positive by chronic fatigue syndrome (CFS) Questionnaire criteria).
• Positive pregnancy test or breast-feeding female.
• Any known allergies to components of the vaccine:
• Formalin
• Eggs or chicken products
• Administration of another vaccine or investigational product within 28 days of skin test and subsequent Q fever vaccination.
• Any unresolved AE resulting from a previous immunization.
• Transplant recipients, subjects with cancer, and those with chronic kidney disease.

Sponsors & Collaborators

• U.S. Army Medical Research and Development Command: lead
• US Army Medical Research Institute of Infectious Diseases: collaborator

Study Sites (1)

Special Immunizations Program, Division of Medicine, USAMRIID

Fort Deterick, Maryland, 21702, United States

Location

MeSH Terms

Conditions

Q Fever

Interventions

Clinical Trials, Phase I as Topic; Desiccation

Condition Hierarchy (Ancestors)

Gram-Negative Bacterial Infections; Bacterial Infections; Bacterial Infections and Mycoses; Infections

Intervention Hierarchy (Ancestors)

Clinical Trials as Topic; Clinical Studies as Topic; Epidemiologic Study Characteristics; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health; Chemistry Techniques, Analytical; Chemical Phenomena

Study Officials

• Mark J Goldberg, MD

  Special Immunizations Program, USAMRIID

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SINGLE GROUP
• Sponsor Type: FED
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 17, 2014
• First Posted: March 20, 2014
• Study Start: February 1, 2006
• Primary Completion: February 1, 2019
• Study Completion: December 1, 2019
• Last Updated: January 2, 2020

Record last verified: 2019-12

Locations

US (1)