drugset / Trial / NCT05918445

PM8002 in the Treatment of Patients With Advanced Solid Tumors

NCT05918445

Phase 1/2 Recruiting 380 enrolled BioNTech SE
NaSequentialOpen-labelTreatment

Summary

This study is to characterize the safety, tolerability, pharmacokinetics (PK), immunogenicity, pharmacodynamics (PD) and anti-tumor activity of PM8002, a PD-L1/VEGF bispecific antibody, as a single agent in adult subjects with advanced solid tumors.

Timeline

Start
2021-03-09
Primary completion
2025-11-30
Completion
2025-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Pumitamig Protein / enzyme biologic Intravenous

Indications