Clinical trial
A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Characteristics of HLX37 (Recombinant Human Bispecific Antibodies Against PD-L1 and VEGF) in Patients With Advanced/Metastatic Solid Tumors
NCT07274813 is registered in ClinicalTrials.gov with Shanghai Henlius Biotech as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Characteristics of HLX37 (Recombinant Human Bispecific Antibodies Against PD-L1 and VEGF) in Patients With Advanced/Metastatic Solid Tumors
- Lead sponsor
- Shanghai Henlius Biotech
- Phase
- Phase 1
- Overall status
- Recruiting
- Start date
- December 29, 2025
- Completion date
- December 30, 2028
- Enrollment
- 254 (estimated)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.
advanced/metastatic solid tumors, nsclc