Clinical trial · Interventional
The Safety and Effectiveness of Cidofovir in the Treatment of Venereal Warts in HIV-Infected Patients
A Phase I/II Study of the Safety and Efficacy of Topical 1-(S)-(3-Hydroxy-2-Phosphonylmethoxypropyl)Cytosine Dihydrate (Cidofovir; HPMPC) in the Treatment of Condyloma Acuminatum in Patients With HIV Infection
NCT00002327CI-TRIAL-00000011completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To evaluate the safety and tolerance of topical cidofovir (HPMPC) therapy for condyloma acuminatum in patients with HIV infection. To investigate whether topical HPMPC therapy can induce regression of condyloma acuminatum in patients with HIV infection.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Condyloma Acuminata | Condyloma Acuminatum | ALIAS | 0.90 |
| HIV Infections | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cidofovir | Drug | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria Concurrent Medication: Allowed: * AZT, ddI, ddC, d4T, or 3TC. * Oral trimethoprim/sulfamethoxazole. * Aerosolized pentamidine. * Dapsone. * Fluconazole. * Rifabutin. * Clarithromycin. Patients must have: * HIV seropositivity. * Mean CD4 count \>= 100 cells/mm3. * External anogenital condyloma acuminatum confirmed by biopsy, present for less than 1 year. NOTE: * Warts on anal, urethral, or vaginal mucosa will not be studied. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Active lesions of genital herpes, other skin wounds, or active inflammatory skin disorders in the same area as warts to be treated. * Active medical problems sufficient to hinder study compliance. Concurrent Medication: Excluded: * Podofilox or any podophyllum resin preparation. * Liquid nitrogen treatment. * Interferon alpha. * Trichloracetic acid. * Other treatments, topical or systemic, surgical or ablative, known to have anti-papilloma activity. * Other investigative drugs (except d4T or 3TC) unless approved by the sponsor. Patients with the following prior conditions are excluded: History of untreated syphilis or Bowenoid papulosis. Prior Medication: Excluded within 4 weeks prior to study entry: * Treatment for anogenital warts. * Immunomodulators (including interferons or systemic corticosteroids). * Lymphocyte replacement therapy. * Biologic response modifiers. Substance abuse.
References
Publications (1)
- BACKGROUNDDouglas J, Corey L, Tyring S, Kriesel J, Bowden B, Crosby D, Berger T, Conant M, McGuire B, Jaffe HS. A phase I/II study of cidofovir topical gel for refractory condyloma acuminatum in patients with HIV infection. Conf Retroviruses Opportunistic Infect. 1997 Jan 22-26;4th:126 (abstract no 334)