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 Randomized, Placebo-Controlled, Double-Blinded Trial of the Safety and Efficacy of Tecovirimat for the Treatment of Human Mpox Virus Disease

Trial Profile

A Randomized, Placebo-Controlled, Double-Blinded Trial of the Safety and Efficacy of Tecovirimat for the Treatment of Human Mpox Virus Disease

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 24 Apr 2026

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 Tecovirimat (Primary)
  • Indications Monkeypox
  • Focus Therapeutic Use
  • Acronyms STOMP

Most Recent Events

  • 27 Mar 2026 According to a European Medicines Agency media release, , CHMP, has recommended that Tecovirimat SIGA should no longer be used for the treatment of mpox followed by the review of data from four studies PALM007, STOMP, UNITY and PLATINUM-UK.
  • 10 Feb 2026 Status changed from active, no longer recruiting to discontinued, due to statistical futility.
  • 12 Mar 2025 Results presented in the ACTG Media Release.

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