A Phase 1b Open-Label Study to Assess the Safety and Pharmacokinetics of Subcutaneously Administered Golimumab, a Human Anti-TNFalpha Antibody, in Pediatric Subjects With Moderately to Severely Active Ulcerative Colitis

Trial Profile

A Phase 1b Open-Label Study to Assess the Safety and Pharmacokinetics of Subcutaneously Administered Golimumab, a Human Anti-TNFalpha Antibody, in Pediatric Subjects With Moderately to Severely Active Ulcerative Colitis

Active, no longer recruiting
Phase of Trial: Phase I

Latest Information Update: 17 Jul 2017

At a glance

  • Drugs Golimumab (Primary)
  • Indications Ulcerative colitis
  • Focus Pharmacokinetics
  • Acronyms PURSUIT-PEDS-PK
  • Sponsors Janssen Research & Development
  • Most Recent Events

    • 24 May 2016 Results assessing pharmacokinetics, efficacy, and safety of golimumab at week 14 presented at the Digestive Disease Week 2016.
    • 27 Nov 2015 Planned primary completion date changed from 1 Oct 2015 to 1 Feb 2017 as reported by ClinicalTrials.gov.
    • 08 Jan 2015 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov .
Restricted Access

Oops, it looks like you don’t have a valid subscription to this content. To gain full access to the content and functionality of the AdisInsight database try one of the following.

  • with a username/password associated to an account with a valid subscription
  • Contact your organization’s admin about adding this content to your AdisInsight subscription
  • Request a trial

If you are a subscriber to this content then contact us at AsktheExpert.AdisInsight@springer.com so we can help.

Back to top