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A Phase IIa, Randomised, Double-blind, Placebo-controlled Trial to Evaluate the Safety, Efficacy, Pharmacokinetics and Pharmacodynamics of BI 706321 Orally Administered for 12 Weeks in Patients With Crohn's Disease (CD) Receiving Ustekinumab Induction Treatment

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Trial Profile

A Phase IIa, Randomised, Double-blind, Placebo-controlled Trial to Evaluate the Safety, Efficacy, Pharmacokinetics and Pharmacodynamics of BI 706321 Orally Administered for 12 Weeks in Patients With Crohn's Disease (CD) Receiving Ustekinumab Induction Treatment

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 06 Sep 2024

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At a glance

  • Drugs BI 706321 (Primary) ; Ustekinumab; Ustekinumab
  • Indications Crohn's disease
  • Focus Therapeutic Use
  • Acronyms InCharge
  • Sponsors Boehringer Ingelheim; Boehringer Ingelheim GmbH International
  • Most Recent Events

    • 19 Aug 2024 Status changed from active, no longer recruiting to discontinued.
    • 29 Apr 2024 Planned primary completion date changed from 24 Jun 2024 to 10 Jul 2024.
    • 19 Apr 2024 This trial has been completed in Denmark, according to European Clinical Trials Database record.

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