Phase I Study of TAK-701 in Adult Patients With Advanced Nonhematological Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

March 31, 2009

Primary Completion Date

November 30, 2010

Study Completion Date

May 31, 2011

Conditions
Advanced Solid Tumors
Interventions
BIOLOGICAL

TAK-701

"Either 2, 5, 10, or 20 mg/kg IV. Cycle 1: single dose at 2x the dose assignment; Cycle 2 and beyond: dose once every two weeks~Dosing continues until disease progression, unacceptable toxicity related to TAK-701, or maximum of 12 cycles, unless determined that patient would benefit from continued therapy."

Trial Locations (3)

19111

Fox Chase Cancer Center, Philadelphia

30322

Emory University School of Medicine, Winship Cancer Institute, Atlanta

37203

The Sarah Cannon Research Institute, Nashville

All Listed Sponsors
lead

Millennium Pharmaceuticals, Inc.

INDUSTRY