Phase I Study of BAY1436032 in IDH1-mutant Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

81

Participants

Timeline

Start Date

May 26, 2016

Primary Completion Date

November 8, 2018

Study Completion Date

December 3, 2024

Conditions
Solid Tumors
Interventions
DRUG

BAY1436032

The selected starting dose of BAY1436032 is 300 mg/day (150 mg BID) to be administered orally continuously in tablet form in 21-day cycles. Adjustments to this schedule may be made if warranted by information collected during the course of the study. The maximum feasible dose of BAY1436032 is expected to be 3000 mg/day.

Trial Locations (13)

2100

København Ø

22903

Charlottesville

45147

Essen

60590

Frankfurt am Main

69115

Heidelberg

72076

Tübingen

77030

Houston

81377

München

90001

Los Angeles

90012

Los Angeles

466-8560

Nagoya

277-8577

Kashiwa

104-0045

Chuo-ku

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY