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, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Effects of EDP-235 in Non-hospitalized Adults With Mild or Moderate COVID-19

Trial Profile

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Effects of EDP-235 in Non-hospitalized Adults With Mild or Moderate COVID-19

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 21 Aug 2024

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 EDP-235 (Primary)
  • Indications COVID 2019 infections
  • Focus Adverse reactions
  • Acronyms SPRINT
  • Sponsors Enanta Pharmaceuticals

Most Recent Events

  • 19 Aug 2024 Status changed from active, no longer recruiting to completed.
  • 17 Apr 2024 According to Enanta Pharmaceuticals media release, data from the study has been accepted for a poster presentation at ESCMID Global 2024 (formerly ECCMID) being held April 27-30 in Barcelona, Spain.
  • 08 May 2023 According to Enanta Pharmaceuticals media release, full data from SPRINT will be presented at a future medical meeting or in a peer-reviewed publication.

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