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A Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Oral ISM4808 in Healthy Adult Subjects in China.

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Oral ISM4808 in Healthy Adult Subjects in China.

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 23 Feb 2026

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At a glance

  • Drugs ISM 4808 (Primary)
  • Indications Anaemia
  • Focus Adverse reactions

Most Recent Events

  • 24 Dec 2025 New trial record
  • 12 Dec 2025 According to a Taigen media release,ISM-4808 received Investigational New Drug (IND) approval from the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) in China in 2023.

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