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A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of QLS7305 Following Subcutaneous Administration in Healthy Chinese Participants.

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Trial Profile

A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of QLS7305 Following Subcutaneous Administration in Healthy Chinese Participants.

Status: Not yet recruiting
Phase of Trial: Phase I

Latest Information Update: 07 Jan 2026

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At a glance

  • Drugs QLS 7305 (Primary)
  • Indications Unspecified
  • Focus Adverse reactions
  • Sponsors Qilu Pharmaceutical

Most Recent Events

  • 07 Jan 2026 New trial record

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