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15-Oct-2019 04:36

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Chief among them would be inebilizumab, the anti-CD19 drug that’s being ushered through the BLA approval process for neuromyelitis optica spectrum disorder, prepped for commercialization and explored in additional indications.

Amgen, which is pushing a biosimilar to the complement inhibitor, filed the IPR in an effort to overturn patents on the composition eculizumab (the active ingredient in Soliris), its formulation, and its use to treat certain diseases, including the key indication of paroxysmal nocturnal hemoglobinuria.Earlier this month Sarepta confirmed to us that the post-marketing study the FDA required in their controversial OK for the Duchenne MD drug Exondys 51 — now on the market at

Amgen, which is pushing a biosimilar to the complement inhibitor, filed the IPR in an effort to overturn patents on the composition eculizumab (the active ingredient in Soliris), its formulation, and its use to treat certain diseases, including the key indication of paroxysmal nocturnal hemoglobinuria.

Earlier this month Sarepta confirmed to us that the post-marketing study the FDA required in their controversial OK for the Duchenne MD drug Exondys 51 — now on the market at $1 million a year — was years behind schedule.

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Amgen, which is pushing a biosimilar to the complement inhibitor, filed the IPR in an effort to overturn patents on the composition eculizumab (the active ingredient in Soliris), its formulation, and its use to treat certain diseases, including the key indication of paroxysmal nocturnal hemoglobinuria.Earlier this month Sarepta confirmed to us that the post-marketing study the FDA required in their controversial OK for the Duchenne MD drug Exondys 51 — now on the market at $1 million a year — was years behind schedule.

million a year — was years behind schedule.



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