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Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
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 Clinical Results associated with Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China)
0 Patents (Medical) associated with Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China)
100 Deals associated with Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China)
100 Translational Medicine associated with Lingke Pharmaceutical (Hangzhou) Co., Ltd. (China)