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, Double-Blind, Placebo-Controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Palmoplantar Pustulosis

Next Previous
Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Phase 2a Study to Evaluate the Efficacy and Safety of RIST4721 in Subjects with Palmoplantar Pustulosis

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 06 Apr 2022

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 RIST 4721 (Primary)
  • Indications Palmoplantar pustulosis
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Aristea Therapeutics

Most Recent Events

  • 30 Nov 2020 Primary endpoint (Relative change in total pustule count) has not been met as per results published in the European Clinical Trials Database Trial Registry
  • 30 Nov 2020 Primary endpoint (Relative change in fresh pustule count) has not been met as per results published in the European Clinical Trials Database Trial Registry
  • 30 Nov 2020 Results published in the European Clinical Trials Database Trial Registry

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