FDA setujui Afrezza untuk pasien diabetes anak

FDA AS telah menyetujui Afrezza bagi anak-anak dan remaja penderita diabetes berusia 6 tahun ke atas. MannKind Corporation mengadakan panggilan konferensi pada 29 Mei 2026, untuk membahas keputusan tersebut.

MannKind Corporation mengumumkan persetujuan tersebut dalam sebuah panggilan yang dipimpin oleh CEO Michael Castagna. Ia menggambarkan hari tersebut sebagai momen bersejarah bagi perusahaan, komunitas diabetes, dan pasien muda. Castagna mencatat bahwa pendiri Al Mann telah lama membayangkan perawatan ini dapat menjangkau anak-anak, dan perusahaan kini memenuhi tujuan tersebut.

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Illustration showing long COVID patients revitalized by fluvoxamine treatment in a clinical trial, with scientists and physician highlighting study results.
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Fluvoxamine eases severe fatigue in long COVID patients

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A study shows the antidepressant fluvoxamine reduces severe fatigue in long COVID patients. In a randomized trial of 399 adults, it was compared with metformin and placebo. Physician Judith Bruchfeld describes the findings as interesting.

A new experimental oral medication called elecoglipron improved blood sugar control and promoted weight loss in adults with type 2 diabetes during a phase 2b trial. Results from the SOLSTICE study were presented at the American Diabetes Association's Scientific Sessions and published in The Lancet.

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The US Food and Drug Administration approved Foundayo, a new once-daily pill for obesity treatment, on Wednesday. Eli Lilly, the manufacturer, also produces the weight-loss injection Zepbound. The approval positions Foundayo as the second obesity pill cleared by the FDA.

A Japanese health panel has approved national health insurance coverage for Sumitomo Pharma's Amchepry, an iPS cell-derived treatment for Parkinson’s disease. The move makes it the world's first commercialized medical product from iPS cells.

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A new treatment called Daraxonrasib has shown strong results against advanced pancreatic cancer in a recent clinical trial. The drug targets a genetic mutation long considered impossible to treat effectively.

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