A Study of TAK-441 in Adult Patients With Advanced Nonhematologic Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

October 31, 2010

Primary Completion Date

December 31, 2012

Study Completion Date

January 31, 2013

Conditions
Advanced Nonhematologic MalignanciesCarcinoma, Basal Cell
Interventions
DRUG

TAK-441

"TAK-441 will be administered as an oral tablet as follows:~Patients enrolled in the dose escalation cohorts will receive:~* A single-dose administration on Day 1, followed by a 1-week washout period during which pharmacokinetics is assessed~* Continuous daily dosing on Days 8 through 28 in Cycle 1~* In subsequent cycles, continuous daily dosing over 21 days, repeated continuously~Patients enrolled in the expansion cohorts will receive continuous daily dosing on Days 1 through 21 of each 21-day cycle"

Trial Locations (2)

90404

Premiere Oncology, A Medical Corporation, Santa Monica

85259-5499

Mayo Clinic, Scottsdale

All Listed Sponsors
lead

Millennium Pharmaceuticals, Inc.

INDUSTRY