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Clinical Trial Summary

PM8002 is a bispecific antibody targeting PD-L1 and VEGF. This study will evaluate the efficacy and safety of PM8002 in combination with paclitaxel as second line treatment for SCLC.


Clinical Trial Description

This is a phase II, single arm study assessing the efficacy and safety of PM8002 in combination with paclitaxel as second line treatment for SCLC who failed first-line platinum-based chemotherapy with or without checkpoint inhibitors therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05879068
Study type Interventional
Source Biotheus Inc.
Contact Jia Song
Phone +86 15921737659
Email song.j@biotheus.com
Status Recruiting
Phase Phase 2
Start date May 27, 2022
Completion date April 30, 2026

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