Minoryx Therapeutics has made a significant step forward in its bid to get lead candidate leriglitazone on the market with EU regulators accepting a file for the drug as a potential treatment for the devastating rare orphan disease, X-linked adrenoleukodystrophy (X-ALD).
The Spanish central nervous system specialist has confirmed that the marketing authorization application for leriglitazone, its oral PPAR gamma agonist, has been validated by the European Medicines Agency and is...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?