Overview

ABI-009 Trial in Patients With Advanced Non-hematologic Malignancies

Status:
Completed
Trial end date:
2011-06-01
Target enrollment:
Participant gender:
Summary
To determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) of ABI-009 given weekly; to characterize the toxicities of ABI-009; and to determine the pharmacokinetic parameters for ABI-009 when given on a weekly schedule.
Phase:
Phase 1
Details
Lead Sponsor:
Celgene
Celgene Corporation
Treatments:
Everolimus
Sirolimus