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一项探索LT-002-158 片在中国化脓性汗腺炎成年患者多次口服的安全性、耐受性、有效性和药代动力学的Ic/II期临床研究
[Translation] A Phase Ic/II clinical study to explore the safety, tolerability, efficacy and pharmacokinetics of LT-002-158 tablets after repeated oral administration in adult patients with hidradenitis suppurativa in China
评价LT-002-158片在中重度化脓性汗腺炎患者中的安全性和耐受性,疗效和药代动力学特征。
[Translation] To evaluate the safety and tolerability, efficacy and pharmacokinetic characteristics of LT-002-158 tablets in patients with moderate to severe hidradenitis suppurativa.
一项探索LT-002-158片在中国特应性皮炎成年受试者多次口服的安全性、耐受性、有效性和药代动力学的Ic/II期临床研究
[Translation] A Phase Ic/II clinical study to explore the safety, tolerability, efficacy and pharmacokinetics of LT-002-158 tablets after repeated oral administration in adult subjects with atopic dermatitis in China
评价LT-002-158片在中重度特应性皮炎受试者中的安全性和耐受性,初步有效性和药代动力学特征。
[Translation] To evaluate the safety and tolerability, preliminary efficacy, and pharmacokinetic characteristics of LT-002-158 tablets in subjects with moderate to severe atopic dermatitis.
/ Not yet recruitingPhase 1/2 A Phase Ic/II Clinical Study to Explore the Safety, Tolerability, Efficacy, and Pharmacokinetics of Multiple Oral Doses of LT-002-158 Tablets in Chinese Adult Patients With Hidradenitis Suppurativa
This study is a Phase Ic/II clinical trial conducted in Chinese patients with moderate-to-severe hidradenitis suppurativa (HS), aiming to evaluate the safety and efficacy of LT-002-158 tablets in the treatment of moderate-to-severe HS.
The study consists of two parts. The Phase Ic portion employs an open-label, single-arm design to primarily investigate the safety and tolerability of LT-002-158 tablets in patients with moderate-to-severe HS. The Phase II study adopts a randomized, double-blind, placebo-controlled, parallel-group design, with an open-label, single-arm extension phase, to primarily assess the therapeutic efficacy of LT-002-158 tablets in patients with moderate-to-severe HS.
100 Clinical Results associated with Leadingtac Pharmaceutical (Shaoxing) Co., Ltd.
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