Hansa Biopharma — Juni 2024
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Sarepta Therapeutics Announces Expanded US FDA Approval of ELEVIDYS to Duchenne Muscular Dystrophy Patients Ages 4 and Above
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Godmorgen
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Kursudviklingen for Sarepta Therapeutics efter børstid kommer ikke til at blive afspejlet direkte, da DMD-aftalen kun udgør en mindre del/værdi af Hansa Biopharmas portefølje, som eksempelvis nævnt i en tidligere analyse fra Penser Access (nu overtaget af Carnegie).
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Sarepta Therapeutics surges 36% after-hours following expanded FDA approval
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Det bliver spændende.
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Sarepta's DMD gene therapy secures much-sought-after label expansion https://firstwordpharma.com/story/5868924
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Sarepta Catapults 30% After Hitting A 'Grand Slam' Approval In Muscular Dystrophy
Sarepta Catapults 30% After Hitting A 'Grand Slam' Approval
Sarepta stock rocketed Friday after hitting a "grand slam" approval that expands the market for its Duchenne muscular dystrophy gene therapy.
Investor's Business Daily (www.investors.com)
"The approval expands the market for Elevidys by more than tenfold, Leerink Partners analyst Joseph Schwartz said. Under the original approval, about 7% of patients were eligible for the gene therapy. Now, about 80% are eligible, he said in a report."
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De bruger det ikke endnu, du har svaret her: https://clinicaltrials.gov/study/NCT06241950?term=Sarepta&aggFilters=status:act&rank=6&tab=history
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Det er ca. 14% af patienter som er potentielle. Ca. 3-400 nyfødte drengebørn i US om året som har DMD. Imlifidase er endnu ikke godkendt i US. Roche står for udrulning af Sareptas genterapi i Europ. Hansa modtager ca 10% i fee,
hvilket svarer til ca.
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