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Safety and Effectiveness of Giving SU5416 to HIV-Infected Patients With AIDS-Related Kaposi's Sarcoma

Not Applicable
Completed
Conditions
Sarcoma, Kaposi
HIV Infections
Registration Number
NCT00002226
Lead Sponsor
SUGEN
Brief Summary

The purpose of this study is to see if it is safe and effective to give SU5416 to HIV-infected patients with AIDS-related Kaposi's sarcoma (KS). SU5416 may prevent the growth of KS tumors.

Detailed Description

Groups of 3-6 patients are sequentially assigned to receive escalating doses of SU5416 in 33% increments. Study drug is administered as a twice-weekly intravenous injection for 4 weeks. In the absence of unacceptable toxicity, responding patients may continue on SU5416 in 4-week treatment cycles for a maximum of 1 year or until the presence of unacceptable toxicity or tumor progression.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

UCLA Care Ctr / Ctr for Hlth Sciences

🇺🇸

Los Angeles, California, United States

Norris Cancer Ctr / USC

🇺🇸

Los Angeles, California, United States

New York Univ Med Ctr

🇺🇸

New York, New York, United States

Saint Francis Mem Hosp / HIV Care Unit

🇺🇸

San Francisco, California, United States

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