drugset / Trial / NCT00531271

ABI-008 Trial in Patients With Metastatic Breast Cancer

NCT00531271 ↗

Phase 1/2 Terminated 85 enrolled Celgene Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLTs) of ABI-008 giver every 3 weeks; to characterize the toxicities of ABI-008; and to determine the pharmacokinetic parameters for ABI-008 when given on an every-3-week schedule to patients with metastatic breast cancer.

Timeline

Start
2007-11-01
Primary completion
2008-12-01
Completion
2008-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject ABI-008 Unknown 60 mg/m2 Intravenous
Subject ABI-008 Unknown 200 mg/m2 Intravenous

Indications