Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01667341
Other study ID # GEN-003-001
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date July 2012
Est. completion date May 9, 2014

Study information

Verified date May 2018
Source Genocea Biosciences, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Randomized, double-blind, placebo-controlled, dose escalation study. There will be 3 cohorts of patients defined by the antigen dose (10, 30 or 100 µg of each antigen), and within each cohort, patients will be randomized at a ratio of 3:1:1 to one of the following:

1. GEN-003/M2: GEN-003 plus Matrix M-2 adjuvant (50 µg per dose)

2. GEN-003: Antigens alone

3. Placebo (DPBS diluent)

Each Cohort is divided into 2 Groups. For each dose cohort, immunizations begin with a Pilot Group. Immunization of the remainder of the Group "Continuation Group") is contingent upon successful review of data from the Pilot Group through Day 7 after immunization. Dose escalation to the next dose level Cohort proceeds after evaluation of safety data from all patients in the prior Cohort and only after all specified safety criteria are met. The total numbers of patients in each Group and Cohort are as follows:

- 10 µg Cohort: 10 Pilot Group, 40 Continuation Group (50 Total)

- 30 µg Cohort: 10 Pilot Group, 40 Continuation Group (50 Total)

- 100 µg Cohort: 10 Pilot Group, 40 Continuation Group (50 Total)

- Totals per group: 30 Pilot Group, 120 Continuation Group (150 Total Patients)

Subjects will receive 3 doses of the assigned treatment (GEN-003/M-2, GEN-003, or placebo) at 3 week intervals. Sampling from mucocutaneous genital sites for viral shedding will be done twice daily for 28 days prior to the first immunization (baseline shedding), and again following the last immunization. Follow-up for safety monitoring will be conducted for 12 months after the last immunization.


Recruitment information / eligibility

Status Completed
Enrollment 143
Est. completion date May 9, 2014
Est. primary completion date May 9, 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Men and women ages 18 to 50 years, inclusive.

- Willing to practice a highly effective method of contraception that includes the use of a barrier method such as a condom.

- Diagnosis of genital HSV-2 infection for > 1 year supported by ONE of the following documented in the medical history or performed at screening:

- Western blot for HSV-2

- Type-specific polymerase chain reaction (PCR) or viral culture

- Compatible clinical history AND HSV-2 ELISA (HerpSelect) index value >3.5

- A history of at least 3 and no more than 9 reported clinical occurrences in the prior 12 months, or, if currently on suppressive therapy, history of at least 3 and no more than 9 reported clinical occurrences in the 12 months prior to initiation suppressive therapy.

- Good general health status as determined by screening evaluation completed within 90 days prior to immunization. Any out of range screening clinical laboratory values should be considered not clinically significant by the Investigator.

- Patient has provided written informed consent.

- Ability and willingness to perform and comply with all study procedures including attending clinic visits as scheduled. Note: patients must provide, by the day of randomization, a minimum of 28 (equivalent of 14 days) baseline viral swab samples to continue to be eligible and be randomized).

Exclusion Criteria:

- On suppressive antiviral medication within 7 days of baseline viral shedding evaluation.

- Immunocompromised individuals, including those receiving systemic corticosteroids or other immunosuppressive agents.

- Positive serologic test for HIV-1 infection; positive hepatitis B surface antigen (HBsAg) or antibody for hepatitis C (anti-HCV).

- Active lesions consistent with herpetic disease at the time of scheduled immunization.

- Pregnant or nursing women.

- Receipt of any investigational drug within 30 days of the first scheduled day of immunization.

- History of hypersensitivity to any component of the vaccine.

- History of genital HSV-1 infection.

- History of: (1) any form of ocular HSV infection, (2) HSV-related erythema multiforme, or (3) herpes meningitis or encephalitis.

- Any other condition which in the opinion of the Investigator would interfere with the successful completion of the study protocol.

- History of drug or alcohol abuse that, in the opinion of the Investigator, would interfere with the patient's ability to comply with the requirements of the study.

- Prior immunization with a vaccine containing HSV-2 antigens.

- Receipt of blood products within 90 days of the first immunization.

Study Design


Intervention

Biological:
GEN-003 with Matrix M-2
IM administration of GEN-003 Vaccine with 50ug Matrix M-2 Adjuvant.
GEN-003
IM administration of GEN-003 Vaccine, antigens alone (without adjuvant).
Placebo
IM administration of 0.5 mL dose of Dulbecco's phosphate buffered saline.

Locations

Country Name City State
United States University of Alabama Vaccine Research Unit Birmingham Alabama
United States Cincinnati Children's Hospital Medical Center Cincinnati Ohio
United States Center for Clinical Studies - Houston Houston Texas
United States Indiana University Infectious Disease Research Indianapolis Indiana
United States Westover Heights Clinic Portland Oregon
United States UW Virology Research Clinic Seattle Washington
United States Center for Clinical Studies - Clear Lake/Webster Webster Texas

Sponsors (1)

Lead Sponsor Collaborator
Genocea Biosciences, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with adverse events as a measure of safety and tolerability 57 Weeks
Secondary Immunogenicity measured by humoral (antibody) and T-cell responses to vaccine antigens 33 weeks
Secondary Change in proportion of days with detectable viral shedding 6 weeks
See also
  Status Clinical Trial Phase
Completed NCT02910284 - Long-term Follow-up of GEN-003-002 Subjects for Efficacy and Immunogenicity N/A
Completed NCT02515175 - Evaluating New Formulation of Therapeutic HSV-2 Vaccine Phase 2
Completed NCT02114060 - Dose Ranging Safety and Efficacy of Therapeutic HSV-2 Vaccine Phase 2
Completed NCT02300142 - Rollover Trial for Placebo Subjects Previously Enrolled Into GEN-003-002 Study Phase 2
Recruiting NCT05432583 - A Clinical Trial in Healthy Volunteers to Study the Safety, Tolerability, and Immune Responses After Vaccination With an Investigational Vaccine Designed to Prevent Genital Herpes Lesions Phase 1
Completed NCT02030301 - Safety and Efficacy Trial of DNA Vaccines to Treat Genital Herpes in Adults Phase 1/Phase 2