Clinical Trial

Phase I Study of HRS-3005 in B-cell Malignancies

Recruiting Phase 1
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Summary
The study is being conducted to evaluate the safety and tolerability of HRS-3005. To explore the Maximum Tolerated Dose (MTD, if possible) and the Recommended Phase 2 Dose (RP2D). This study also preliminarily evaluated the efficacy of HRS-3005 in patients with B-cell malignancy.
Protocol Amendment History 1 change
critical Recruitment opened 2026-06-11
Trial Details
NCT Number NCT07556822
Lead Sponsor Jiangsu HengRui Medicine Co., Ltd.
Conditions B-cell Malignancy
Enrollment 190 participants
Start Date 2026-06-03
Primary Completion 2028-10 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2026-06-10