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A Randomized, Single-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety and Tolerability of ALRN-5281 Administered by Subcutaneous Injection in Healthy Adult Volunteers

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Trial Profile

A Randomized, Single-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety and Tolerability of ALRN-5281 Administered by Subcutaneous Injection in Healthy Adult Volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 24 Jan 2025

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At a glance

  • Drugs ALRN 5281 (Primary)
  • Indications Somatotropin deficiency
  • Focus Adverse reactions
  • Sponsors Aileron Therapeutics; Rein Therapeutics

    • Most Recent Events

    • 10 Jan 2025 According to Rein Therapeutics media release, Aileron Therapeutics announces rebranding to Rein Therapeutics
    • 04 Dec 2013 New trial record

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