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.
Four groups of 10 patients each receive topical HPMPC at 0.3 percent concentration for 5 or 10 days total or 1.0 percent concentration for 5 or 10 days total, followed by 2 weeks of rest. When six patients at a given dose and schedule have completed treatment and follow-up without significant toxicity, subsequent patients are entered at the next higher dose level. Patients are evaluated twice weekly during treatment and once weekly during the rest period. HPMPC may be extended for up to two additional courses in patients who experience no significant toxicity.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Enrollment
40
East Bay AIDS Ctr
Berkeley, California, United States
Univ California San Francisco
San Francisco, California, United States
City and County of Denver / Dept of Health & Hosps
Denver, Colorado, United States
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Univ of Rochester Med Ctr
Rochester, New York, United States
Bronx-Lebanon Hosp Ctr
The Bronx, New York, United States
Houston Clinical Research Network
Houston, Texas, United States
Dr Brad Bowden
Houston, Texas, United States
Dr Stephen Tyring
Nassau Bay, Texas, United States
Univ of Utah School of Medicine
Salt Lake City, Utah, United States
Univ of Washington / Viral Disease Clinic
Seattle, Washington, United States
...and 1 more locations