Yiming Angko-B (01541.HK): IMM01 (tidapecip) combined with azacitidine was approved by the State Drug Administration to conduct a randomized, double-blind, controlled phase III clinical trial plan

Gelonghui Finance · May 17 04:37

Gelonghui, May 17 | Yiming Angko-B (01541.HK) issued an announcement. The Group was approved by the Drug Evaluation Center of the State Drug Administration (“Drug Evaluation Center”) to conduct a randomized, double-blind, controlled IMM01 (tidapecip) combined with azacitidine phase III clinical trial plan for first-line treatment of high-risk myelodysplastic syndrome (HRMDS). Furthermore, the latest results of the IMM01 (tidapecip) combined with azacitidine phase II clinical trial program have been accepted as an oral report to be presented at the 2024 American Society of Clinical Oncology (“ASCO”) conference to be held in Chicago on June 1, 2024.

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宜明昂科-B(01541.HK)：IMM01(替达派西普)联合阿扎胞苷获国家药监局批准进行随机、双盲、对照III期临床试验方案

Yiming Angko-B (01541.HK): IMM01 (tidapecip) combined with azacitidine was approved by the State Drug Administration to conduct a randomized, double-blind, controlled phase III clinical trial plan

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