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Clinical Trial Summary

This is a multicenter, single-arm phase II study to evaluate the efficacy and safety of CS1001 monotherapy for relapsed/refractory classical Hodgkin Lymphoma (rr-cHL)


Clinical Trial Description

Eligible subjects with rr-cHL who failed at least two prior lines of therapies are planned to receive CS1001 1200 mg intravenous infusion every three weeks until progression of disease, intolerable toxicity, consent withdrawn or death.The primary endpoint of this trial is objective response rate (ORR), as assessed by independent radiological review committee (IRRC) based on Criteria for Response Assessment of Lymphoma: Lugano 2014 Classification. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03505996
Study type Interventional
Source CStone Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date May 22, 2018
Completion date November 1, 2021

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