A Phase 1, Multicenter, Open-label, Dose-increasing Study to Evaluate the Safety, Tolerability, PK/PD and Preliminary Efficacy of Y101D, a Recombinant Anti-PD-L1 and TGF-β Bispecific Antibody for Injection, in Patients With Metastatic or Locally Advanced Solid Tumors
Latest Information Update: 19 Feb 2024
At a glance
- Drugs Y 101 D (Primary)
- Indications Solid tumours
- Focus Adverse reactions
- Sponsors YZY Biopharma
- 11 Feb 2024 Planned End Date changed from 6 Aug 2023 to 6 Aug 2024.
- 11 Feb 2024 Planned primary completion date changed from 6 Aug 2022 to 15 Mar 2024.
- 11 Feb 2024 Status changed from recruiting to active, no longer recruiting.