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Clinical Trial Summary

PM8002 is a bispecific antibody targeting PD-L1 and VEGF. This study to evaluate the efficacy and safety of PM8002 in combination with etoposide and platinum in first-line treatment of extensive-stage small cell lung cancer


Clinical Trial Description

The study is divided into two parts. The first part is single-arm study, with a planned enrollment of at least 59 subjects. The second part is randomized, double-blind study, this study plans to enroll 386 subjects, who will be randomized in a 1:1 ratio to an experimental group of PM8002 in combination with chemotherapy (etoposide and platinum) and a control group of Atezolizumab with chemotherapy (etoposide and platinum). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05844150
Study type Interventional
Source Biotheus Inc.
Contact Zhishuo Cheng
Phone +86 021 32120207
Email cheng.zs@biotheus.com
Status Recruiting
Phase Phase 2/Phase 3
Start date June 1, 2023
Completion date December 2025

See also
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