Cardiol To Test Oral Cannabidiol Formulation In Acute Myocarditis Patients

  • The FDA has signed off Cardiol Therapeutics Inc's CRDL Investigational New Drug (IND) application for CardiolRx.
  • Cardiol will commence a Phase 2, multi-center, double-blind, randomized, placebo-controlled trial to assess the safety and tolerability of CardiolRx in acute myocarditis patients.
  • Myocarditis is an acute inflammatory condition of the myocardium, characterized by inflammation of the heart muscle.
  • The study will enroll 100 patients.
  • The primary endpoints of the trial, which will be evaluated after 12 weeks of double-blind therapy, consist of left ventricular function (ejection fraction and longitudinal strain) and myocardial edema (extra-cellular volume).
  • CardiolRx is a pharmaceutically produced oral cannabidiol formulation investigated in Phase 2/3 outcomes study (the LANCER trial) to evaluate CardiolRx as a cardioprotective therapy to reduce mortality and major cardiovascular events.
  • Related content: Benzinga's Full FDA Calendar.
  • Price Action: CRDL shares are up 9.90% at $3.33 during the premarket session on the last check Tuesday.
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