Expired Study
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Menlo Park, California 94025


To provide Stealth liposomal doxorubicin hydrochloride ( DOX-SL ) as a therapy for Kaposi's sarcoma patients who have no remaining treatment options other than DOX-SL or patients who have been participating in another DOX-SL protocol and for whom continuation in DOX-SL is medically indicated. Also, to evaluate the safety and efficacy of DOX-SL in patients with Kaposi's sarcoma who have previously received systemic chemotherapy with or without an anthracycline.

Study summary:

Patients receive DOX-SL every 3 weeks for up to 20 cycles.


Inclusion Criteria Patients must have: - AIDS-related Kaposi's sarcoma that requires systemic chemotherapy. - EITHER a medical indication for continuation of DOX-SL following treatment on another DOX-SL protocol, OR no remaining treatment options other than DOX-SL. Prior Medication: Allowed: - Prior anthracyclines. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: - Cardiac ejection fraction < 50 percent or clinically significant cardiac disease. - Eligibility for a Liposomal Technology comparative protocol. Concurrent Medication: Excluded: - Other cytotoxic chemotherapy. Patients with the following prior condition are excluded: History of idiosyncratic or allergic reaction to anthracyclines. Prior Medication: Excluded: - Chemotherapy within the past 3 weeks.



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Backup Contact:


Location Contact:

Menlo Park, California 94025
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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