An Non-randomized Open-label, Multicenter Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, Preliminary Efficacy of BA1301in Participants With Advanced Solid Tumors
Latest Information Update: 22 Apr 2025
At a glance
- Drugs BA-1301 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Shandong Boan Biotechnology
- 15 Apr 2025 Status changed from planning to recruiting.
- 14 Jan 2023 New trial record
- 09 Jan 2023 According to a Luye Pharma Group media release, Boan Biotech has received the approval for clinical trials by the Center for Drug Evaluation (CDE) of China's National Medical Products Administration (NMPA).