An Open-label, Non-randomized, Multicenter Phase I Study to Determine the Maximum Tolerated or Recommended Phase II Dose of Oral Mutant IDH1 Inhibitor BAY1436032 and to Characterize Its Safety, Tolerability, Pharmacokinetics and Preliminary Pharmacodynamic and Anti-tumor Activity in Patients With IDH1-R132X-mutant Advanced Solid Tumors
Latest Information Update: 20 Dec 2024
At a glance
- Drugs BAY 1436032 (Primary)
- Indications Astrocytoma; Cholangiocarcinoma; Chondrosarcoma; Glioblastoma; Glioma; Oligodendroglioma; Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Bayer
- 18 Dec 2024 Status changed from active, no longer recruiting to completed.
- 06 Aug 2023 Planned End Date changed from 29 Dec 2023 to 31 Dec 2024.
- 01 Aug 2022 Planned End Date changed from 31 Dec 2022 to 29 Dec 2023.