Drugs / SYH2082
last change Apr 2026 re-read 3 minutes ago

SYH2082

Investigated by
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07532655 Apr → Oct 2026 expected obesity disorder CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Not yet recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2026-03-20 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - GLP-1/GIP RECEPTOR DUAL-BIASED AGONIST POLYPEPTIDE LONG-ACTING INJECTION (SYH2082 INJECTION) OBTAINS CLINICAL TRIAL APPROVAL IN CHINA irasia.com ↗
GLP-1/GIP RECEPTOR DUAL-BIASED AGONIST POLYPEPTIDE LONG-ACTING INJECTION (SYH2082 INJECTION) OBTAINS CLINICAL TRIAL APPROVAL IN CHINA
2026-02-16 CSPC ZhongQi Pharmaceutical Technology Co., Ltd. Regulatory VOLUNTARY ANNOUNCEMENT - GLP-1/GIP RECEPTOR DUAL-BIASED AGONIST POLYPEPTIDE LONG-ACTING INJECTION (SYH2082 INJECTION) OBTAINS CLINICAL TRIAL APPROVAL IN THE U.S. 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 has obtained approval from the U.S. Food and Drug Administration (FDA) to conduct clinical trials in the U.S. with GLP-1/GIP receptor dual-biased agonist polypeptide long- acting injection (SYH2082 Injection) developed by the Group.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as SYH2082 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07532655 ↗
Route Subcutaneous “A subcutaneous injection in the abdomen” NCT07532655 ↗