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NCT06792955

The Evaluation of Bioequivalence Between a Single-dose Pen and a Multi-dose Pen of HRS9531 Injection Solution

Completed Phase 1 Last updated 12 June 2025
What this trial tests

Phase 1 trial testing HRS9531 injection in Overweight/Obesity in 120 participants. Completed in 6 June 2025.

Timeline
11 February 2025
Primary endpoint
6 June 2025
6 June 2025

Quick facts

Lead sponsorFujian Shengdi Pharmaceutical Co., Ltd.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment120
Start date11 February 2025
Primary completion6 June 2025
Estimated completion6 June 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Shengdi Pharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 18 to 45, any sex, with Overweight/Obesity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study is being conducted to evaluate the bioequivalence between a single-dose pen and a multi-dose pen of HRS9531 injection solution.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of HRS9531 injection

Trials testing the same drug.

Other recruiting trials for Overweight/Obesity

Currently open trials in the same condition.

Other Fujian Shengdi 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/NCT06792955.

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