Overview

A Study of BL-M11D1 in Patients With Relapsed/Refractory Acute Myeloid Leukemia

Status:
Recruiting
Trial end date:
2025-08-01
Target enrollment:
Participant gender:
Summary
Ia: To observe the safety and tolerability of BL-M11D1 in patients with relapsed/refractory acute myeloid leukemia to determine the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT) of BL-M11D1. Ib: Further observe the safety and tolerability of BL-M11D1 at the recommended dose in phase Ia to determine the recommended dose in phase II clinical study (RP2D).
Phase:
Phase 1
Details
Lead Sponsor:
Sichuan Baili Pharmaceutical Co., Ltd.