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A Phase I, Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of CM383 Following Intravenous and Subcutaneous Administration in Healthy Adult Subjects

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Trial Profile

A Phase I, Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of CM383 Following Intravenous and Subcutaneous Administration in Healthy Adult Subjects

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 28 Jan 2026

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At a glance

  • Drugs CM 383 (Primary) ; CM 383 (Primary)
  • Indications Alzheimer's disease
  • Focus Pharmacokinetics
  • Sponsors KeyMed Biosciences

Most Recent Events

  • 23 Jan 2026 Planned initiation (estimated date of first participant enrollment) date changed from 1 Dec 2025 to 1 Jan 2026.
  • 23 Jan 2026 Status changed from not yet recruiting to recruiting.
  • 25 Dec 2025 New trial record

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