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?

Single Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Effects of SR-878 in Healthy Volunteers

Trial Profile

Single Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Effects of SR-878 in Healthy Volunteers

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 10 Jun 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 SR-878 (Primary)
  • Indications Autoimmune disorders; Inflammatory bowel diseases; Rheumatoid arthritis
  • Focus Adverse reactions; First in man
  • Sponsors SciRhom

Most Recent Events

  • 03 Jun 2025 Status changed from recruiting to discontinued. Reason the study was stopped: Sponsor decision.
  • 02 Dec 2024 Status changed from not yet recruiting to recruiting.
  • 17 Oct 2024 According to a SciRhom media release, the company announced the initiation of the first patient dosing in this trial, with readouts expected in the second half of 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