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一项评估AX-023治疗复发或难治性淋巴瘤患者的安全性、耐受性、药代动力学特征和初步有效性的剂量递增和扩展I期临床研究
[Translation] A Phase I dose-escalation and expansion study to evaluate the safety, tolerability, pharmacokinetic profile and preliminary efficacy of AX-023 in patients with relapsed or refractory lymphoma
Ia期:评价AX-023在复发或难治性淋巴瘤受试者中的安全性和耐受性,并探索AX-023的剂量限制性毒性(DLT)、最大耐受剂量(MTD)或II期推荐剂量(RP2D)。
Ib期:评价AX-023治疗选定瘤种类型的有效性。
[Translation] Phase Ia: Evaluate the safety and tolerability of AX-023 in subjects with relapsed or refractory lymphoma, and explore the dose-limiting toxicity (DLT), maximum tolerated dose (MTD) or recommended dose for Phase II (RP2D) of AX-023.
Phase Ib: Evaluate the efficacy of AX-023 in the treatment of selected tumor types.
100 Clinical Results associated with Beijing Anxin Huaide Biotechnology Co., Ltd
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100 Deals associated with Beijing Anxin Huaide Biotechnology Co., Ltd
100 Translational Medicine associated with Beijing Anxin Huaide Biotechnology Co., Ltd