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Masitinib AB Science (masitinib)

Orphan
Region
🇪🇺 EU
Active substance
masitinib
Company
AB Science
Status
Refused
Therapeutic area
Amyotrophic Lateral Sclerosis
CHMP opinion
Thu 27 Jun 2024
Designations
Orphan
Application
EMEA/H/C/005897
ATC
L01EX06
Official record
www.ema.europa.eu

Indication

In combination with riluzole for the treatment of adult patients with amyotrophic lateral sclerosis (ALS)

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.