Eplontersen fda approval

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Actual: FDA Approves WAINUA (Eplontersen) for Treatment of Hereditary ATTR Amyloidosis Polyneuropathy BREAKING NEWS: The U.S. Food and Drug Administration has approved AstraZeneca and Ionis WAINUA (eplontersen) for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults, commonly referred to as hATTR-PN or ATTRv-PN.

4.6 rating 2025-04-24

Comments

User8164

Did the author obtain approval of the FDA to post?

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User5264

You do realize that silicone breast implants were banned by the FDA in 1992, right?

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User1170

As I began mentally selling my billions, though, I realized that the FDA would never allow this product to be sold, and that most likely I'd have to do testing on my own.
What the hell would the FDA have to do with it? This is a piece of machinery. They would have NO say about it whatsoever.

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FDA for the treatment of transthyretin-mediated amyloid cardiomyopathy (ATTR-CM) in adults. Eplontersen was previously approved for the

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The FDA has approved vutrisiran (Amvuttra), patisiran (Onpattro), inotersen (Tegsedi), and eplontersen (Wainua) for treatment of polyneuropathy

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Decem - AstraZeneca and Ionis announced the FDA approval of Wainua (eplontersen), for the treatment of the polyneuropathy of

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In December 2024, the FDA approved eplontersen, a ligand conjugated antisense oligonucleotide, as a treatment for patients with ATTRv-PN.

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The FDA has granted regulatory approval for WAINUA for the Wainua (eplontersen; Ionis, Astrazeneca) is currently the only approved

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The FDA has approved eplontersen (Wainua) to treat hereditary transthyretin-mediated amyloidosis (hATTR)-associated polyneuropathy.

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The United States Food and Drug Administration (FDA) has approved AstraZeneca and Ionis' Wainua (eplontersen) for treating polyneuropathy of

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FDA approved for the treatment of the cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis (ATTR-CM). Eplontersen

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WAINUA (eplontersen) Approved in US for Adult Polyneuropathy in Hereditary Transthyretin Amyloidosis In the United States, the FDA has

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