FSD Pharma Inc. (NASDAQ: HUGE), a biopharma company developing innovative assets and biotech solutions for the treatment of neurodegenerative, inflammatory and metabolic disorders, announced the first cohort of participants on its Phase 1 study assessing Lucid-21-302, or Lucid-MS, has completed dosing.

Conducted by the company’s wholly-owned subsidiary Lucid Psycheceuticals, the randomized, double-blind, placebo-controlled and both single- and multiple-ascending dose trial aims to assess Lucid-MS, a small molecule inhibitor of hypercitrullination, as a …

Full story available on Benzinga.com

A note to our visitors

This website has updated its privacy policy in compliance with changes to European Union data protection law, for all members globally. We’ve also updated our Privacy Policy to give you more information about your rights and responsibilities with respect to your privacy and personal information. Please read this to review the updates about which cookies we use and what information we collect on our site. By continuing to use this site, you are agreeing to our updated privacy policy.