A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics (PK) of TAK-228 as Single Agent in Adult East Asian Participants With Advanced Nonhematological Malignancies
Stopped More favorable safety profile was observed in QD schedule, therefore further enrollment in QW schedule was terminated.
Conditions
- Advanced Nonhematological Neoplasms
Interventions
Sponsor
Calithera Biosciences, Inc