New ETF Book by Larry Connors - Click here to read more
The Orphan Drug Designation for Duchenne muscular dystrophy (DMD) entitles AMT to a ten year market exclusivity in Europe following marketing approval for AMT-080, if this product candidate is the first new drug with a major medical benefit receiving marketing approval for the European Union.
The designation also provides for special benefits, including research support, eligibility for protocol assistance and possible exemptions or reductions in certain regulatory fees during development or at the time of application for marketing approval.
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