Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Phase 2 Open-Label Study to Evaluate the Efficacy and Safety of Ustekinumab, a Human Monoclonal Anti-IL-12/IL-23 Antibody, in Patients With Behcet Disease

Trial Profile

A Phase 2 Open-Label Study to Evaluate the Efficacy and Safety of Ustekinumab, a Human Monoclonal Anti-IL-12/IL-23 Antibody, in Patients With Behcet Disease

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 13 Dec 2021

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Ustekinumab (Primary)
  • Indications Behcet's syndrome; Genital ulcer; Oral ulcer; Panuveitis; Posterior uveitis; Retinal disorders; Vasculitis
  • Focus Proof of concept; Therapeutic Use
  • Acronyms STELABEC

Most Recent Events

  • 02 Dec 2021 Primary endpoint has been met (Number of oral ulcers at week 24 compared to baseline)as per Results published in the Journal of the American Academy of Dermatology
  • 02 Dec 2021 Results published in the Journal of the American Academy of Dermatology
  • 12 Nov 2020 Status changed from active, no longer recruiting to completed.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top