drugset / Trial / NCT05028556
A Trial of Y101D, a PD-L1/TGF-β Bispecific Antibody, in Patients With Metastatic or Locally Advanced Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is a phase 1, multicenter, open-label study to evaluate the safety, tolerability, PK, PD, immunogenicity and preliminary efficacy of Y101D in patients with metastatic or locally advanced solid tumors.
Timeline
- Start
- 2021-08-06
- Primary completion
- 2024-07-05
- Completion
- 2024-09-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Y101D | Unknown | 1 mg/kg | Intravenous |
| Subject | Y101D | Unknown | 3 mg/kg | Intravenous |
| Subject | Y101D | Unknown | 10 mg/kg | Intravenous |
| Subject | Y101D | Unknown | 20 mg/kg | Intravenous |
| Subject | Y101D | Unknown | 30 mg/kg | Intravenous |