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Completed Phase 2 Interventional

Comparison of Liposomal Doxorubicin Used Alone or in Combination With Bleomycin Plus Vincristine in the Treatment of Kaposi's Sarcoma in Patients With AIDS

ClinicalTrials.gov ID: NCT00001059

Public ClinicalTrials.gov record NCT00001059. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 6:52 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Comparison Study of Liposomal Doxorubicin With or Without Bleomycin and Vincristine for the Treatment of Advanced AIDS-Associated Kaposi's Sarcoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the safety and efficacy of liposomal doxorubicin hydrochloride ( DOX-SL ) alone or in combination with bleomycin and vincristine in the long-term treatment of AIDS-related Kaposi's sarcoma. To determine whether the 3-drug combination enhances progression-free survival and quality of life. Liposomal formulations of chemotherapeutic agents increase drug accumulation in tumors, which permits disease palliation at relatively low doses and thus decreases some of the dose-limiting toxicity. Multi-agent therapy is considered to be more effective than single-agent therapy; therefore, DOX-SL will be combined with bleomycin and vincristine.

Study identification

NCT ID
NCT00001059
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
120 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Aug 1998 (Actual)
Last update posted
Apr 17, 2012

Ends 1998

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Alabama Therapeutics CRS Birmingham Alabama 35294 —
USC CRS Los Angeles California 90033 —
UCLA CARE Center CRS Los Angeles California 90095 —
Ucsf Aids Crs San Francisco California — —
University of Colorado Hospital CRS Aurora Colorado 80262 —
Univ. of Miami AIDS CRS Miami Florida 33136 —
Queens Med. Ctr. Honolulu Hawaii 96813 —
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816 —
Northwestern University CRS Chicago Illinois 60611 —
Rush Univ. Med. Ctr. ACTG CRS Chicago Illinois 60612 —
Indiana Univ. School of Medicine, Infectious Disease Research Clinic Indianapolis Indiana 46202 —
Bmc Actg Crs Boston Massachusetts 02118 —
Beth Israel Deaconess - East Campus A0102 CRS Boston Massachusetts 02215 —
Massachusetts General Hospital ACTG CRS Boston Massachusetts — —
Washington U CRS St Louis Missouri 63110 —
SUNY - Buffalo, Erie County Medical Ctr. Buffalo New York 14215 —
Memorial Sloan-Kettering Cancer Ctr. New York New York 10021 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00001059, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 17, 2012 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00001059 live on ClinicalTrials.gov.

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