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?

Phase 1 randomized, double-blinded, placebo controlled, dose escalation clinical trial of MF-300 in healthy adults

X
Trial Profile

Phase 1 randomized, double-blinded, placebo controlled, dose escalation clinical trial of MF-300 in healthy adults

Status: Planning
Phase of Trial: Phase I

Latest Information Update: 27 Dec 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 MF 300 (Primary)
  • Indications Sarcopenia
  • Focus Adverse reactions
  • Most Recent Events

    • 27 Dec 2024 New trial record
    • 23 Dec 2024 According to Epirium Bio media release, U.S. Food and Drug Administration (FDA) has cleared the Companys Investigational New Drug (IND) application for MF-300, a first-in-class orally administered, 15-hydroxyprostaglandin dehydrogenase (15-PGDH) enzyme inhibitor in development for the treatment of sarcopenia, or age-induced muscle weakness
    • 23 Dec 2024 According to Epirium Bio media release,the company expects to deliver MF-300 Phase 1 results in H2 2025

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