A Study of B1962, a PD-L1/VEGF Bispecific Antibody Fusion Protein, for Advanced Solid Tumors
A Multicenter, Open-label, Dose-escalating Phase I Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Profile of B1962 Injection in the Treatment of Advanced Malignant Solid Tumors
Sponsor: Tasly Biopharmaceuticals Co., Ltd.
Listed as NCT05650385, this PHASE1 trial focuses on Neoplasms Malignant and remains ongoing. Sponsored by Tasly Biopharmaceuticals Co., Ltd., it has been updated 4 times since 2022, reflecting limited change activity. This study contributes to the evolving evidence base for cancer treatment protocols.
Status Flow
Change History
4 versions recorded-
Dec 2025 — Present [monthly]
Unknown PHASE1
Status: Not Yet Recruiting → Unknown
-
Sep 2024 — Dec 2025 [monthly]
Not Yet Recruiting PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Not Yet Recruiting PHASE1
-
Jan 2023 — Jul 2024 [monthly]
Not Yet Recruiting PHASE1
First recorded
Dec 2022
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Tasly Biopharmaceuticals Co., Ltd.
For direct contact, visit the study record on ClinicalTrials.gov .