7
Participants
Start Date
October 31, 2007
Primary Completion Date
September 30, 2009
Study Completion Date
September 30, 2009
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.
Memorial Sloan-Kettering Cancer Center, New York
Rebecca and John Moores UCSD Cancer Center, La Jolla
Beth Israel Deaconess Medical Center, Boston
National Cancer Institute (NCI)
NIH
The Emmes Company, LLC
INDUSTRY
AIDS Malignancy Consortium
NETWORK