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最高研发阶段临床2期 |
首次获批国家/地区- |
首次获批日期- |
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficiency and Safety of LNK01001 Capsule in Patients With Ankylosing Spondylitis
The objective of this study was to evaluate the safety and efficacy of multiple doses of LNK01001 monotherapy versus placebo in the treatment of adults with active Ankylosing Spondylitis
An Open-Label, Multicenter, Phase I Study to Evaluate the Safety, Pharmacokinetics and Preliminary Efficacy of LNK01002 in Patients With Malignant Myeloid Hematologic Neoplasms
This multicenter, open-label, phase 1 study designed to evaluate safety and tolerability of multi-kinase inhibitor LNK01002 in patients with primary myelofibrosis (PMF), or MF due to polycythemia vera (PV-MF), or essential thrombocythemia (ET-MF), polycythemia vera (PV), or with acute myeloid leukemia (AML).
100 项与 Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China) 相关的临床结果
0 项与 Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China) 相关的专利(医药)
100 项与 Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China) 相关的药物交易
100 项与 Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China) 相关的转化医学