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 2b, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of EDP-938 in Non-hospitalized Adults with Acute Respiratory Syncytial Virus Infection Who Are At High Risk for Complications

Trial Profile

A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of EDP-938 in Non-hospitalized Adults with Acute Respiratory Syncytial Virus Infection Who Are At High Risk for Complications

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 09 Jul 2025

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 Zelicapavir (Primary)
  • Indications Respiratory syncytial virus infections; Respiratory tract infections
  • Focus Therapeutic Use
  • Acronyms RSVHR
  • Sponsors Enanta Pharmaceuticals

Most Recent Events

  • 01 Jul 2025 Status changed from active, no longer recruiting to completed.
  • 05 Jun 2025 Status changed from recruiting to active, no longer recruiting.
  • 12 May 2025 According to an Enanta Pharmaceuticals media release, trial met target enrollment of 180 participants for RSVHR and plan to complete enrollment in late May to capture the remainder of the current Northern Hemisphere RSV season. Company is on track to report topline data in late 3Q 2025.

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