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 1b/2a study of fezagepras for patients with high triglyceride levels (hypertriglyceridemia)

X
Trial Profile

A phase 1b/2a study of fezagepras for patients with high triglyceride levels (hypertriglyceridemia)

Status: Discontinued
Phase of Trial: Phase I/II

Latest Information Update: 03 Jun 2021

Price : $35 *
  • 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 Fezagepras (Primary)
  • Indications Hypertriglyceridaemia
  • Focus Adverse reactions; Therapeutic Use
  • Most Recent Events

    • 28 May 2021 According to a Liminal BioSciences media release, based on the interim pharmacokinetic results from the ongoing Fezagepras multiple ascending dose (MAD) study, the company has decided to stop its plans to move fezagepras into a phase Ia/IIb study in Hypertriglyceridemia.
    • 28 May 2021 Status changed from planning to discontinued, according to Liminal BioSciences media release.
    • 17 May 2021 According to a Liminal BioSciences media release, the company expects to initiate this study in the 2022.

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
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