A Safety Study of Two Dapivirine (TMC120) Vaginal Gels in the United States

International Partnership for Microbicides (IPM)

Status and phase: Completed; Phase 2; Phase 1

Conditions: HIV-1 Infections

Treatments: Drug: Drug placebo; Drug: dapivirine gel 4759; Drug: dapivirine 4789

Study type: Interventional

Funder types: Industry

Identifiers

NCT00799058

IPM 020

Details and patient eligibility

About

A double-blind, randomized, placebo-controlled Phase I/II trial to evaluate the safety of dapivirine Gel 4759, 0.05% 2.5 g and dapivirine Gel 4789, 0.05% 2.5 g formulations as compared to the vaginal HEC-based Universal placebo gel, 2.5 g in healthy HIV-negative women

Full description

This was a double-blind, randomized, placebo-controlled trial, to be conducted over 10 months at five research centers in the USA among 180 healthy, sexually active women, to assess the safety and acceptability of dapivirine Gel 4759, 0.05% 2.5 g, and dapivirine Gel 4789, 0.05% 2.5 g, both vaginal microbicides containing dapivirine, compared to the vaginal HEC-based Universal placebo gel, 2.5 g, containing no active ingredient, used once daily for a period of 12 weeks.

Enrollment: 128 patients

Sex: Female

Ages: 18 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Women 18 to 40 years of age inclusive who can give written informed consent

2. Available for all visits and consent to follow all procedures scheduled for the trial

3. Healthy and self-reported sexually active

4. HIV-negative as determined by an HIV test at time of enrollment

5. Willing to be on a stable form of contraception

6. In the absence of the use of exogenous hormone(s), have a self-reported regular menstrual cycle

7. Upon pelvic/speculum examination and colposcopy at the enrollment visit, the cervix and vagina appear normal as determined by qualified research center staff

8. Asymptomatic for genital infections at the time of enrollment

9. Willing to refrain from use of vaginal products or objects for 14 days prior to enrollment and for the duration of the trial.

10. Documentation of no abnormality on Pap smear within 90 days prior to randomization;

11. Willing to answer acceptability and adherence questionnaires throughout the trial

12. Willing to refrain from participation in any other research trial for the duration of this trial

13. Willing to provide adequate locator information for trial retention purposes and be reachable per local standard procedures

14. Willing to abstain from all the following criteria beginning 48 hours prior to each trial visit:

    • Vaginal intercourse
    • Oral contact with her genitalia
    • Internal vaginal washing
    • Penetration of the vagina by fingers, sex toys, or any other objects, including medications

15. Willing to abstain from all of the following for 3 days after biopsy procedures:

    • Vaginal intercourse
    • Oral contact with her genitalia
    • Internal vaginal washing
    • Penetration of the vagina by fingers, sex toys, or any other objects, including medications

Exclusion criteria

1. Currently pregnant or having had their last pregnancy outcome within 3 months prior to screening
2. Currently breast-feeding, or having breastfed within 3 months prior to screening
3. Receipt of any investigational agent within 60 days prior to screening
4. Previously participated in any HIV vaccine trial
5. Untreated urogenital infections within 2 weeks prior to enrollment
6. Presence of any abnormal physical finding on the vulva, vaginal walls or cervix during pelvic/speculum examination and/or colposcopy
7. History of significant urogenital or uterine prolapse, undiagnosed vaginal bleeding, or urethral obstruction
8. Pap smear result at screening that requires cryotherapy, biopsy or treatment (other than for infection)
9. History of symptomatic or asymptomatic HSV-2
10. Any Grade 2, 3 or 4 hematology, chemistry or urinalysis laboratory abnormality at baseline
11. Unexplained, undiagnosed abnormal bleeding per vagina during or following vaginal intercourse; or urogenital surgery within 90 days prior to enrollment
12. Any history of anaphylaxis or severe allergy resulting in angioedema; or a history of sensitivity/allergy to latex
13. Any serious acute, chronic or progressive disease
14. Any condition(s) that, in the opinion of the Investigator, might interfere with adherence to trial requirements or evaluation of the trial objectives

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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128 participants in 3 patient groups, including a placebo group

dapivirine gel 4789

Active Comparator group

Description:

will be applied by participants once daily for 12-weeks treatment period

Treatment:

Drug: dapivirine 4789

dapivirine gel 4759

Active Comparator group

Description:

Will be applied by participants once daily for12-weeks treatment period

Treatment:

Drug: dapivirine gel 4759

HEC-based placebo gel, 2.5g containing no Dapivirine

Placebo Comparator group

Description:

Will be applied once daily for 12-weeks treatment period

Treatment:

Drug: Drug placebo