Drugs / HS-10542
Trials 3
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 11 trial | ||||||
| Phase 1 | NCT07040046 | May → Dec 2025 overdue | — | Jiangsu Hansoh Pharmaceutical Co., Ltd. | Recruiting | No outcome recorded |
| Phase 1/21 trial | ||||||
| Phase 1/2 | NCT07470762 | Feb 2026 → May 2027 expected | paroxysmal nocturnal hemoglobinuria | Jiangsu Hansoh Pharmaceutical Co., Ltd. | Recruiting | No outcome recorded |
| Phase 21 trial | ||||||
| Phase 2 | NCT07474636 | Mar 2026 → Dec 2027 expected | IgA glomerulonephritis | Jiangsu Hansoh Pharmaceutical Co., Ltd. | Not yet recruiting | No outcome recorded |
News releases announcing trial results or a regulatory action · 2
| Date | Issuer | Release |
|---|---|---|
| 2026-03-30 | Hansoh BioMedical R&D Company | Results WCN 2026 | 翰森制药HS-10542(补体因子B抑制剂)健康参与者Ⅰ期临床数据发布 hansoh.cn ↗ |
| 2026-03-28 | Jiangsu Hansoh Pharmaceutical Co., Ltd. | Results WCN 2026 | HANSOH PHARMA PRESENTED PHASE 1 DATA OF HS-10542(A COMPLEMENT FACTOR B INHIBITOR)IN HEALTHY PARTICIPANTS hspharm.com ↗
Nearly complete inhibition (>95%) was achieved at 24 hours after last dosing of MAD across doses. |
All press releases naming this drug 2 releases
| Date | Issuer | Release |
|---|---|---|
| 2026-03-30 | Hansoh BioMedical R&D Company | WCN 2026 | 翰森制药HS-10542(补体因子B抑制剂)健康参与者Ⅰ期临床数据发布 hansoh.cn ↗ |
| 2026-03-28 | Jiangsu Hansoh Pharmaceutical Co., Ltd. | WCN 2026 | HANSOH PHARMA PRESENTED PHASE 1 DATA OF HS-10542(A COMPLEMENT FACTOR B INHIBITOR)IN HEALTHY PARTICIPANTS hspharm.com ↗ |
Evidence & citations 4 cited values
Every value below carries the sentence it was read from. 3 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | HS-10542 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT07474636 ↗ |
| Action | Inhibit | “inhibits factor B (FB)” NCT07470762 ↗ |
| Modality | Small molecule | “HS-10542 is a novel oral small molecular weight compound” NCT07470762 ↗ |
| Route | Oral | “administered orally once on Day 1” NCT07040046 ↗ |