A Safety and Tolerability Study of Dapivirine (TMC120) Vaginal Microbicide Gel

International Partnership for Microbicides (IPM)

Status and phase

Completed

Phase 2

Phase 1

Conditions

HIV Infections

Treatments

Drug: dapivirine (TMC120) vaginal gel

Study type

Interventional

Funder types

Industry

Identifiers

NCT00303576

IPM003

Details and patient eligibility

About

Approximately 112 HIV-negative women, aged 18 to 50, will be enrolled in this multicenter study at four sites. Volunteers will be randomized to dapivirine (TMC120) vaginal gel or matching placebo gel. The volunteers will receive investigational product for a total of 42 days. Volunteers will be monitored on days 7, 28 and 42 for safety, tolerability and compliance.

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

HIV-negative
Willing to participate and sign an informed consent
Willing to be tested for HIV, use an experimental vaginal gel, and to be randomized to a study group that includes the possibility of being assigned to a placebo group.
Willing to use two forms of contraception during the study.
Willing to undergo pelvic examinations with colposcopy and photographic documentation according to the protocol throughout the study.
Have a regular menstrual cycle defined as having a minimum of 21 days and a maximum of 36 days between menses.
Willing to abstain from using any vaginal product (other than the study product or placebo).
Willing to be sexually abstinent from randomization until completion of Day 7 evaluations.

Exclusion criteria

Currently pregnant or breast-feeding.
Clinically detectable genital abnormality on the vulva, vaginal walls or cervix.
Laboratory confirmed gonorrhea, chlamydia, trichomonas, syphilis, or vaginal candidiasis or clinically diagnosed genital ulcer disease or active HSV-2 lesions.
Breakthrough bleeding or gynecologic surgery within 60 days prior to randomization.
Symptomatic bacterial vaginosis and unwilling to undergo treatment.
Women who require treatment for tuberculosis (TB) within 21 days prior to randomization.