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A 14 Week Phase 2b, Randomized, Double-Blind, Dose-Ranging Study to Determine the Pharmacokinetics, Efficacy, Safety and Tolerability of TEV-48574 in Adult Patients With Ulcerative Colitis or Crohn's Disease (RELIEVE UCCD)

Trial Profile

A 14 Week Phase 2b, Randomized, Double-Blind, Dose-Ranging Study to Determine the Pharmacokinetics, Efficacy, Safety and Tolerability of TEV-48574 in Adult Patients With Ulcerative Colitis or Crohn's Disease (RELIEVE UCCD)

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 21 Mar 2025

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At a glance

  • Drugs Duvakitug (Primary)
  • Indications Crohn's disease; Ulcerative colitis
  • Focus Therapeutic Use
  • Acronyms RELIEVE UCCD
  • Sponsors Teva Branded Pharmaceutical Products R&D

Most Recent Events

  • 22 Feb 2025 According to a Sanofi media release, company presented new, detailed results from the RELIEVE UCCD phase 2b study in two oral presentations at the 20th Congress of the European Crohns and Colitis Organisation (ECCO) in Berlin, Germany.
  • 22 Feb 2025 Results presented in the sanofi media release.
  • 18 Feb 2025 According to a Teva Pharmaceutical Industries media release, company will conduct a conference call and live webcast at 8 am E.T. on Monday, February 24, 2025 discuss new data presented for duvakitug (anti-TL1A) positive Phase 2b results at the 20th Annual Congress of the European Crohn's and Colitis Organization (ECCO).

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