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NCT07232758

Safety, Tolerability and Pharmacokinetic Studies of HRS-2183 for Injection in Healthy Chinese Subjects After Single and Multiple Administration

Recruiting now Phase 1 Last updated 14 November 2025
What this trial tests

Phase 1 trial testing HRS-2183 in Chinese Healthy Adult Subjects in 42 participants. Currently enrolling.

Timeline
30 October 2025
Primary endpoint
1 February 2026
1 February 2026

Quick facts

Lead sponsorJiangsu HengRui Medicine Co., Ltd.
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment42
Start date30 October 2025
Primary completion1 February 2026
Estimated completion1 February 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Jiangsu HengRui Medicine Co., Ltd. — full company profile →

Who can join

Adults 18 to 45, any sex, with Chinese Healthy Adult Subjects. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study mainly evaluated the safety and tolerability, as well as the pharmacokinetic characteristics, of the injectable drug HRS-2183 after single and multiple administrations in healthy subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Jiangsu HengRui Medicine Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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