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NCT07519109

Study Evaluating the Safety, Efficacy and Pharmacokinetics of SYH9089 Injection in Patients Undergoing Abdominal Surgery.

Not yet recruiting Phase 1 Last updated 9 April 2026
What this trial tests

Phase 1 trial testing SYH9089 injection in Postoperative Pain in 60 participants. Not yet recruiting.

Timeline
31 March 2026
Primary endpoint
31 December 2026
31 March 2027

Quick facts

Lead sponsorCSPC Ouyi Pharmaceutical Co., Ltd.
PhasePhase 1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment60
Start date31 March 2026
Primary completion31 December 2026
Estimated completion31 March 2027

Drugs / interventions tested

Conditions studied

Sponsor

CSPC Ouyi Pharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 18 to 75, any sex, with Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomized, double-blind, active drug- and placebo-controlled, dose-escalation clinical study conducted in patients scheduled to undergo abdominal surgery. It aims to evaluate the tolerability, safety, pharmacokinetics, and efficacy of SYH9089 Injection for postoperative analgesia in these patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Postoperative Pain

Currently open trials in the same condition.

Other CSPC Ouyi Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07519109.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing