Last updated: 11/07/2018 11:32:33
A Study to Investigate the Efficacy and Safety of Valaciclovir in the Treatment of Recurrent Ano-Genital Herpes in HIV-Infected Patients
Clinicaltrials.gov ID
Not applicable
EudraCT ID
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EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Study to Investigate the Efficacy and Safety of Valaciclovir in the Treatment of Recurrent Ano-Genital Herpes in HIV-Infected Patients
Trial description: A Study to Investigate the Efficacy and Safety of Valaciclovir in the Treatment of Recurrent Ano-Genital Herpes in HIV-Infected Patients
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Conant MA, Schacker TW, Murphy RL, Gold J, Crutchfield LT, Crooks RJ, and the International Valaciclovir HSV Study Group. “Valaciclovir versus acyclovir for herpes simplex virus infection in HIV-infected individuals: two randomized trials”. International Journal of STS & AIDS, 13: 12-21; 2002.
Valacyclovir for the Suppression of Ano-Genital Herpes Simplex Virus (HSV) Infection in HIV-Infected Persons Schacker, T; Wald, A; DeJesus, E, and Warren, T. 40th Annual Meeting of the Infectious Diseases Society of America; Chicago, IL; USA. 2002 Oct 24
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1995-26-04
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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