U.S., May 14 -- ClinicalTrials.gov registry received information related to the study (NCT07583212) titled 'Phase I Study of HRS-1635 in B-cell Malignancies' on May 07.
Brief Summary: The study is being conducted to evaluate the safety and tolerability of HRS-1635. To observe the Dose-Limiting Toxicity (DLT) , explore the Maximum Tolerated Dose (MTD, if possible) and the Recommended Phase 2 Dose (RP2D). This study also preliminarily evaluated the efficacy of HRS-1635 in participants with B-cell malignancy.
Study Start Date: June, 2026
Study Type: INTERVENTIONAL
Condition:
B-cell Malignancy
Intervention:
DRUG: HRS-1635
HRS-1635
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Chengdu Suncadia Medicine Co., Ltd.
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