Drugs / SYHA1813
last change May 2026 re-read 8 days ago

SYHA1813

Developed for
meningioma
Investigated by
Shanghai Runshi Pharmaceutical Technology Co., Ltd

Trials 4

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT06157918 Dec 2023 → Jan 2024 — Shanghai Runshi Pharmaceutical Technology Co., Ltd Completed No outcome recorded
Phase 1/21 trial
Phase 1/2 NCT06682611 Nov 2024 → Nov 2026 expected — Shanghai Runshi Pharmaceutical Technology Co., Ltd Not yet recruiting No outcome recorded
Phase 21 trial
Phase 2 NCT06739213 Jan 2025 → Jan 2027 expected meningioma Shanghai Runshi Pharmaceutical Technology Co., Ltd Not yet recruiting No outcome recorded
Phase 31 trial
Phase 3 NCT07613450 May 2026 → Jul 2029 expected meningioma Shanghai Runshi Pharmaceutical Technology Co., Ltd Not yet recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2020-11-03 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - INNOVATIVE DRUG "SYHA1813 ORAL SOLUTIONS" OBTAINS CLINICAL TRIAL APPROVAL irasia.com ↗
The board of directors (the “ Board”) of CSPC Pharmaceutical Group Limited (the “ Company ”, together with its subsidiaries, the “ Group”) is pleased to announce that the Group’s Category 1 innovative drug “SYHA1813 Oral Solutions” (the “ Product ”) has obtained approval granted by the National Medical Products Administration of the People’s Republic of China to conduct clinical trials in China.

All press releases naming this drug 1 release

DateIssuerRelease

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as SYHA1813 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06739213 ↗
3

NCT07613450 ↗

NCT06682611 ↗

NCT06157918 ↗

Route Oral “SYHA1813 oral solution, 25mg, oral” NCT06157918 ↗