Clinical Study to Evaluate the Maximum Tolerated Dose of BAY1000394 Given in a 3 Days on / 4 Days Off Schedule in Subjects With Advanced Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

112

Participants

Timeline

Start Date

August 31, 2010

Primary Completion Date

June 30, 2016

Study Completion Date

December 31, 2016

Conditions
Neoplasms
Interventions
DRUG

Roniciclib (BAY1000394)

Oral administration twice daily in a 3 days on / 4 days off schedule. Starting dose will be 0.3 mg corresponding to approximately 0.005 mg/kg and dose will be escalated dependent on any dose limiting toxicities.

Trial Locations (9)

13915

Marseille

14033

Caen

44195

Cleveland

44625

Herne

63110

St Louis

69008

Lyon

69120

Heidelberg

94805

Villejuif

14263-0001

Buffalo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY