Title

Botswana Study of UC-781 Vaginal Microbicide
Phase I Trial of the Safety, Toxicity, and Acceptability of the Microbicide UC-781 When Topically Applied by HIV-uninfected Women and Men in Botswana
  • Phase

    Phase 1
  • Study Type

    Interventional
  • Status

    Withdrawn
  • Intervention/Treatment

    uc-781 ...
  • Study Participants

    0
This study will test the safety, side effects, and acceptability of two strengths of UC-781 gel when used by women and men in Botswana for two weeks.
45 women and 45 men, all healthy and sexually active, 21-45 years old, without HIV infection, will be enrolled in Francistown and Gaborone, Botswana. Volunteers will be randomized to receive either 0.1% or 0.25% UC-781 carbomer gel or placebo gel (3 arms. Women will be instructed to apply gel intravaginally, morning and evening, and prior to sex (always with male condom use) for 14 consecutive days. Men will be instructed to apply gel topically for 14 consecutive nights, before bed, allow to dry overnight, and wash it off in the morning. Additionally instructed never to use gel during sex but always to use condoms. Volunteers will be seen weekly for evaluation of symptoms, laboratory toxicities, genital exam findings (with colposcopy for women, and plasma drug levels. Acceptability will be assessed in focus groups in the month after completing gel use.
Study Started
Oct 05
2006
Last Update
Aug 16
2012
Estimate

Drug UC-781 carbomer gel, 0.1% and 0.25%

Criteria

Inclusion Criteria:

21-45 years old
citizen of Botswana
willing to use condoms for 14 days
PAP smear (normal, inflammation, ASCUS)
regular menses or amenorrhea
lives within 1 hour of a study clinic
pass comprehension test
provide written informed consent

Exclusion Criteria:

genital mucosal disruption at screening
genital surgery within past 8 weeks
pregnant within past 8 weeks
currently breastfeeding
prior hysterectomy
plans to move within 2 months
ALT, AST, total bilirubin, or creatinine Grade 2 or above
Prothrombin or partial thromboplastin time Grade 2 or above
In other drug/vaccine safety trial
Has more than one sexual partner in past month
Unwilling/unsure they can have sex at least twice weekly for 2 weeks
Any other condition that investigator believes will interfere with the evaluation of study objectives
No Results Posted