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Clinical Trial Summary

This is an open-label, multi-center Phase II study designed to evaluate the efficacy and safety of Surufatinib plus anti-PD-1/L1 as maintenance therapy after first-line standard of care in patients with ES-SCLC.


Clinical Trial Description

This study consists of two parts, i.e., a single-arm Phase IIa study and a randomized, controlled Phase IIb study. All the enrolled patients will be patients with ES-SCLC who did not have PD (determined as per the RECIST v1.1) after prior platinum-based chemotherapy in combination with an anti-PD-1/L1. Approximately 20 patients are planned to be enrolled in the single-arm Phase IIa study to preliminarily observe the efficacy and safety. Approximately 40 patients are planned to be enrolled in the randomized and controlled Phase IIb study with 20 patients per group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05509699
Study type Interventional
Source Hutchmed
Contact Hannah Yang, Master
Phone 86 21 2067 1962
Email hannahy@hutch-med.com
Status Recruiting
Phase Phase 2
Start date September 27, 2022
Completion date December 2024

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