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: 05 Aug 2025
At a glance
- Drugs Y 101 D (Primary)
- Indications Solid tumours
- Focus Adverse reactions
- Sponsors YZY Biopharma
Most Recent Events
- 20 Jul 2025 Status changed from active, no longer recruiting to completed.
- 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.