A Safety and Pharmacokinetic Study of TAK-285 in Patients With Advanced Cancer

PHASE1CompletedINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

August 31, 2007

Primary Completion Date

June 30, 2011

Study Completion Date

June 30, 2011

Conditions
Cancer
Interventions
DRUG

TAK-285 Dose Escalation Cohorts

TAK-285 50 mg tablet, orally, once or twice daily for three weeks, followed by seven days off. Dose escalation to maximum tolerated dose, with possibility of continuous dosing per cycle (daily dosing for four weeks without a break between cycles).

DRUG

TAK-285 Recommended Phase 2 Dosing Cohort

Expanded cohort with dose and regimen dependent upon the safety profile of the maximally tolerated dose and schedule determined in the dose escalation phase of the study.

Trial Locations (3)

21201

University of Maryland Greenbaum Cancer Center, Baltimore

46202

Indiana University Cancer Center, Indianapolis

48201

Karmanos Cancer Center, Detroit

All Listed Sponsors
lead

Millennium Pharmaceuticals, Inc.

INDUSTRY