Drugs / HS-10374
last change 20 days ago re-read 9 days ago

HS-10374

Developed for
psoriasis · psoriatic arthritis
Investigated by
Hansoh BioMedical R&D Company · Jiangsu Hansoh Pharmaceutical Co., Ltd.

Trials 6

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT07181343 May → Jun 2025 psoriasis Hansoh BioMedical R&D Company Completed No outcome recorded
Phase 1 NCT06033742 Nov 2021 → Mar 2023 psoriasis Jiangsu Hansoh Pharmaceutical Co., Ltd. Completed No outcome recorded
Phase 23 trials
Phase 2 NCT06926582 Apr 2025 → Jul 2026 overdue psoriasis Hansoh BioMedical R&D Company Not yet recruiting No outcome recorded
Phase 2 NCT06176508 Feb 2024 → Apr 2026 overdue psoriatic arthritis Hansoh BioMedical R&D Company Recruiting No outcome recorded
Phase 2 NCT06077331 Sep 2023 → Jul 2024 psoriasis Hansoh BioMedical R&D Company Unknown No outcome recorded
Phase 31 trial
Phase 3 NCT06672393 Nov 2024 → Oct 2025 overdue psoriasis Hansoh BioMedical R&D Company Not yet recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 5

DateIssuerRelease
2026-09-21 Jiangsu Hansoh Pharmaceutical Co., Ltd. Results HANSOH PHARMA ANNOUNCES PIVOTAL PHASE 3 CLINICAL TRIAL OF HS-10374 IN THE TREATMENT OF ADULTS WITH MODERATE-TO-SEVERE PLAQUE PSORIASIS MET THE CO-PRIMARY ENDPOINTS hspharm.com ↗
Pivotal Phase 3 clinical trial of HS-10374 met co-primary endpoints in adults with moderate-to-severe plaque psoriasis, with both PASI 75 and sPGA 0/1 response rates significantly higher than those in the placebo group at week 16.
2024-11-29 Jiangsu Hansoh Pharmaceutical Co., Ltd. Results HANSOH PHARMA PRESENTS POSITIVE PHASE II CLINICAL STUDY OF HS-10374, IN PATIENTS WITH MODERATE-TO-SEVERE PLAQUE PSORIASIS AT CDA 2024 hspharm.com ↗
HS-10374 showed significant clinical efficacy versus Placebo (PBO) in terms of PASI 75 response rate and sPGA 0/1 response rate with oral doses of 6 mg QD or 12 mg QD in patients with moderate-to-severe plaque psoriasis.
2024-11-29 Hansoh BioMedical R&D Company Results CDA 2024 | 翰森制药TYK2抑制剂HS-10374用于治疗中重度斑块状银屑病的Ⅱ期临床研究积极数据发布 hansoh.cn ↗
本次CDA大会发表的研究数据显示,当HS-10374口服剂量为6mg QD或12mg QD时,其在中重度斑块状银屑病患者中可达到显著高于安慰剂的PASI 75应答率和sPGA 0/1应答率,有效性显著.
2024-10-10 Jiangsu Hansoh Pharmaceutical Co., Ltd. Results EADV 2024 | HANSOH PHARMA RELEASED THE PHASE II CLINICAL STUDY DATA OF HS-10374,IN PATIENTS WITH MODERATE-TO-SEVERE PLAQUE PSORIASIS hspharm.com ↗
The recently published clinical trial results of HS-10374 showed significant clinical efficacy versus PBO in terms of PASI 75 response rate and sPGA 0/1 response rate with oral doses of ≥6 mg in patients with moderate-to-severe plaque psoriasis.
2024-10-10 Hansoh BioMedical R&D Company Results EADV 2024 | 翰森制药HS-10374 Ⅱ期研究数据获口头报告,用于治疗中重度斑状银屑病 hansoh.cn ↗
本 次 在EADV大 会 发 表 的 研 究 数 据 显 示,在 中 重 度 斑 块 状 银 屑 病 患 者 中,HS-10374有 效 性 显 著,整 体 安 全 性 与 其 他TYK2抑 制 剂 相 似,且 皮 肤 毒 性 风 险 较 低.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as HS-10374 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06033742 ↗
5

NCT06077331 ↗

NCT06176508 ↗

NCT06672393 ↗

NCT06926582 ↗

NCT07181343 ↗

Route Oral “Single or multiple dosing of HS-10374 orally in a fasting state” NCT06033742 ↗