Study of TAK-733 in Adult Patients With Advanced Nonhematologic Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

December 31, 2009

Primary Completion Date

April 30, 2013

Study Completion Date

June 30, 2013

Conditions
Advanced Non-hematologic MalignanciesAdvanced Metastatic Melanoma
Interventions
DRUG

TAK-733

"The Initial Escalation Stage will enroll approximately 30 patients with advanced nonhematologic malignancies. TAK-733 will be administered orally in 28-day treatment cycles consisting of intermittent dosing with 21 days of continuous treatment, followed by a rest period of 7 days.~The Expansion Stage will enroll approximately 30 patients with advanced metastatic melanoma. The recommended phase 2 dose determined in the Initial Escalation Stage of TAK-733 will be administered orally in 28-day treatment cycles consisting of intermittent dosing with 21 days of continuous treatment, followed by a rest period of 7 days."

Trial Locations (2)

14263

Roswell Park Cancer Institute, Buffalo

48201

Wayne State University Karmanos Cancer Institute, Detriot

All Listed Sponsors
lead

Millennium Pharmaceuticals, Inc.

INDUSTRY