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A Randomized, Double Blind, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of CM310 in Patients With Moderate-to-severe Atopic Dermatitis

Trial Profile

A Randomized, Double Blind, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of CM310 in Patients With Moderate-to-severe Atopic Dermatitis

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 11 Nov 2024

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At a glance

  • Drugs Stapokibart (Primary)
  • Indications Atopic dermatitis
  • Focus Registrational; Therapeutic Use
  • Sponsors KeyMed Biosciences

Most Recent Events

  • 08 Nov 2024 Status changed from active, no longer recruiting to completed.
  • 12 Sep 2024 According to KeyMed Biosciences media release, the National Medical Products Administration of China has recently approved the new drug application for Stapokibart (anti-IL-4Ra monoclonal antibody, trade name: Kangyueda for the indication of moderate-to-severe atopic dermatitis in adults.
  • 02 Jun 2024 According to KeyMed Biosciences media release, company announced the long-term efficacy and safety data of a Phase III clinical trial of stapokibart injection in patients with moderate-to-severe atopic dermatitis (AD) has been released by way of oral presentation at the European Academy of Allergy and Clinical Immunology (EAACI) Congress 2024.

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