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Zacks Investment Research on MSNAlnylam Gets FDA Nod for Expanded Use of Amvuttra in CardiomyopathyAlnylam Pharmaceuticals ALNY announced that the FDA had approved its regulatory filing seeking the label expansion of its ...
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Zacks Investment Research on MSNPharma Stock Roundup: PFE's Final Haleon Stake Sale, AZN, SNY M&A DealsThis week, the FDA approved J&J’s JNJ Tremfya for its second inflammatory bowel disease (“IBD”) condition, Crohn’s disease ...
Novartis was announced as an official partner of this year’s Eurovision competition last fall, after the song entry from Switzerland won the 2024 iteration, making it the host country for the ...
Novartis' Fabhalta receives FDA approval for C3 glomerulopathy, expanding its kidney disease portfolio as global regulatory ...
The FDA on Thursday approved Fabhalta (iptacopan) to treat complement 3 glomerulopathy (CG3), a progressive, ultrarare kidney ...
From new hires to departures, promotions and transfers, here are the latest comings and goings in the pharmaceutical industry ...
This is the third indication for Fabhalta after Novartis won FDA approval of the small molecule in paroxysmal nocturnal hemoglobinuria and primary immunoglobulin A nephropathy.
Novartis' Fabhalta has become the first treatment approved by the FDA for the ultra-rare kidney disease C3G. But analysts spotted several shortfalls in the drug's label, leaving more to be desired—and ...
The FDA approved oral iptacopan (Fabhalta; Novartis) to reduce proteinuria in adults with C3 glomerulopathy (C3G), according ...
Data incorporated for this study were collected from 9 centers in the UK focused on third-line and beyond chimeric antigen ...
Novartis has a third FDA-approved indication for its oral therapy for complement-mediated diseases – Fabhalta – after getting ...
The U.S. Health and Human Services Department is weighing plans to drastically cut federal government funding for domestic ...
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