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Kyndrisa ()

Generic
Region
🇪🇺 EU
Company
BioMarin International Limited
Status
Application withdrawn
Therapeutic area
Muscular Dystrophy, Duchenne
Designations
Generic
Application
EMEA/H/C/003846
ATC
M09AX04
Official record
www.ema.europa.eu

Indication

Treatment of Duchenne muscular dystrophy (DMD).

Regulatory milestones

No milestones recorded in the last year.

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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.