drugset / Trial / NCT00322400

Phase1b to Evaluate Safety of AMG706 in Combination With Paclitaxel or Docetaxel for Breast Cancer

NCT00322400

Phase 1 Completed 46 enrolled Amgen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This open-label, dose-finding, multi-center study is designed to determine the safety and the maximum tolerated dose of AMG 706 given once daily in combination with either weekly paclitaxel (Arm A) or once-every-3 week docetaxel (Arm B) in subjects with locally recurrent or metastatic breast cancer. Secondarily, this study will evaluate the pharmacokinetic (PK) profile of AMG 706 in both treatment arms, the PK profile of paclitaxel in Arm A and the PK profile of docetaxel in Arm B. Additionally, this study will assess objective tumor response and duration of response. Exploratory endpoints include the investigation of potential biomarker development and to assess the effects of genetic variation in drug metabolism genes, cancer genes and drug target genes on subject response to AMG 706 in combination with paclitaxel or docetaxel.

Timeline

Start
2006-03
Primary completion
2009-04
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2
Subject Docetaxel Small molecule 100 mg/m2
Subject Paclitaxel Small molecule 90 mg/m2
Subject motesanib Small molecule 50 mg Oral
Subject motesanib Small molecule 75 mg Oral
Subject motesanib Small molecule 100 mg Oral
Subject motesanib Small molecule 125 mg Oral