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A Phase I, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of Subcutaneous Administration of Single Ascending Doses of HRS-5817 in Obese Participants

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Trial Profile

A Phase I, Randomized, Double-blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of Subcutaneous Administration of Single Ascending Doses of HRS-5817 in Obese Participants

Status: Recruiting
Phase of Trial: Phase 0

Latest Information Update: 20 Jan 2026

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At a glance

  • Drugs HRS 5817 (Primary)
  • Indications Obesity
  • Focus Adverse reactions
  • Sponsors Atridia

Most Recent Events

  • 16 Jan 2026 Status changed from not yet recruiting to recruiting.
  • 01 Dec 2025 New trial record

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