Logo

Mitsubishi Tanabe Pharma America Reports 48-Week P-III Trial (MT-1186-A01) Results of Radicava ORS (edaravone) for Amyotrophic Lateral Sclerosis

Share this
Mitsubishi Tanabe Pharma

Mitsubishi Tanabe Pharma America Reports 48-Week P-III Trial (MT-1186-A01) Results of Radicava ORS (edaravone) for Amyotrophic Lateral Sclerosis

Shots:

  • The P-III trial (MT-1186-A01) evaluating the long-term safety and tolerability of Radicava ORS (edaravone) in 185 patients with ALS for ~48wks. of treatment across 50 sites in the US, Canada, EU, and Japan. The study was funded and conducted by MTPA and MTDA
  • The results showed that Radicava ORS was well tolerated with no new safety signals. The study results were published in Muscle & Nerve, no serious TEAEs were reported, the discontinuation rate during the treatment period was 25%, and TEAEs led to treatment discontinuation was 8.6%. These results were based on the 24wk. results
  • Additionally, Radicava ORS was approved in the US on May 2022, as an oral suspension form of edaravone

Ref: PRNewswire | Image: Mitsubishi Tanabe

Related News:- EditForce Entered into a License Agreement with Mitsubishi Tanabe Pharma to Develop and Commercialize Gene Therapies for Central Nervous System

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions