Condition: Solid Tumor · Non Hodgkin Lymphoma · Sponsor: Jiangsu Simcere Pharmaceutical Co., Ltd.
A Phase 1, open label, multi center, dose escalation and expansion study will assess the safety, tolerability, PK, and preliminary efficacy of SCR-6920 capsule in participants with advanced malignant tumors. The purpose of the study is to identify the maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D), and to confirm the tolerability and preliminary efficacy of SCR-6920 in participants with advanced solid tumors and relapsed/refractory non-Hodgkin lymphoma(NHL).
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| Shandong Cancer Hospital | Jinan, Shandong, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05528055