Phase I Study to Investigate Pharmacokinetics and Safety of BAY73-4506 in Asian (Japanese) Patients With Solid Tumors.

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

July 1, 2009

Primary Completion Date

April 26, 2010

Study Completion Date

November 11, 2013

Conditions
Tumors
Interventions
DRUG

Regorafenib (BAY73-4506)

The patients will be treated on Day 1 of the first week followed by 6 days off treatment (Cycle 0, single dosing period). After Cycle 0, the patients will be treated with BAY 73-4506 (160 mg once daily orally, 21 days on/ 7 days off schedule). Dose level : 160 mgDose level-1: 120 mgDose level-2: 60 mg

Trial Locations (4)

277-8577

Kashiwa-shi

350-1298

Hidaka

104-0045

Chuo-ku

181-8611

Mitaka

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY