Sirolimus in Treating Patients With HIV-Related Kaposi's Sarcoma

PHASE1CompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

September 30, 2009

Study Completion Date

September 30, 2009

Conditions
Sarcoma
Interventions
DRUG

sirolimus

The target rapamycin trough level will be 5-10 ng/mL. The initial dose will be dependent upon the type of HAART regimen. Subjects will continue on study protocol for six cycles as long as their KS is stable or continuing to respond to study medication. Treatment will be extended for up to six additional cycles if the subject has met criteria for a response. Subjects with no more than stable disease will have treatment discontinued after six cycles. Protocol treatment will be discontinued if the subject develops tumor progression, unacceptable toxicity or develops one of the protocol-defined reasons for treatment discontinuation at any time during the study.

Trial Locations (3)

10065

Memorial Sloan-Kettering Cancer Center, New York

92093-0658

Rebecca and John Moores UCSD Cancer Center, La Jolla

02215

Beth Israel Deaconess Medical Center, Boston

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

collaborator

The Emmes Company, LLC

INDUSTRY

lead

AIDS Malignancy Consortium

NETWORK

NCT00450320 - Sirolimus in Treating Patients With HIV-Related Kaposi's Sarcoma | Biotech Hunter | Biotech Hunter