Supernus provides regulatory update for SPN-830

8 April 2024 - Supernus Pharmaceuticals today announced a regulatory update for SPN-830. ...

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Stealth BioTherapeutics announces FDA acceptance of new drug application for elamipretide for the treatment of Barth syndrome

8 April 2024 - If approved, elamipretide would become the first approved therapy for Barth syndrome. ...

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Phanes Therapeutics' PT217 granted fast track designation by the FDA

8 April 2024 - Phanes Therapeutics announced today that the US FDA has granted fast track designation to PT217 for the ...

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ARS Pharmaceuticals submits response to FDA complete response letter for neffy (epinephrine nasal spray)

3 April 2024 - Submission of complete response letter response triggers up to six month review period by the FDA. ...

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FDA grants breakthrough therapy designation to sunvozertinib for the first-line treatment of patients with advanced non-small cell lung cancer harboring EGFR exon 20 insertion mutations

7 April 2024 - Dizal today announced that the US FDA has granted breakthrough therapy designation to its sunvozertinib as ...

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FDA grants accelerated approval to fam-trastuzumab deruxtecan-nxki for unresectable or metastatic HER2 positive solid tumours

5 April 2024 - Today, the FDA granted accelerated approval to fam-trastuzumab deruxtecan-nxki (Enhertu, Daiichi Sankyo) for adult patients with ...

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Amylyx Pharmaceuticals announces formal intention to remove Relyvrio/Albrioza from the market

4 April 2024 - Based on top-line results from the Phase 3 PHOENIX trial of AMX0035 in ALS, Amylyx has started ...

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FDA accepts supplemental biologics license applications for Bimzelx (bimekizumab-bkzx) for moderate to severe hidradenitis suppurativa and additional 2 mL device presentations

4 April 2024 - Application in moderate to severe hidradenitis suppurativa based on results from two Phase 3 studies where ...

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Vanda Pharmaceuticals' Fanapt (iloperidone) receives US FDA approval for the acute treatment of bipolar I disorder

2 April 2024 - Fanapt treatment is now available to adult patients for the acute treatment of manic or mixed episodes ...

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FDA approves new antibiotic for three different uses

3 April 2024 - Today, the US FDA approved Zevtera (ceftobiprole medocaril sodium for injection) for the treatment of adults with ...

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RemeGen's telitacicept (RC18) granted fast track designation by US FDA for treatment of primary Sjögren's syndrome

2 April 2024 - RemeGen has obtained fast track designation by the US FDA recently for its innovative BLyS/APRIL dual-target ...

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Zanidatamab biologics license application for previously treated HER2 positive metastatic biliary tract cancer completed

2 April 2024 - Zymeworks is pleased to announce, along with our partners Jazz Pharmaceuticals, completion of the rolling submission of ...

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TME Pharma receives US FDA fast track designation for lead asset NOX-A12 in brain cancer

2 April 2024 - Fast track designation for NOX-A12 follows recently announced FDA clearance of investigational new drug application for Phase ...

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Datopotamab deruxtecan biologics license application accepted in the US for patients with previously treated metastatic HR positive, HER2 negative breast cancer

2 April 2024 - Application based on results from the TROPION-Breast01 Phase 3 trial. ...

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Voydeya approved in the US as add-on therapy to ravulizumab or eculizumab for treatment of extravascular haemolysis in adults with the rare disease PNH

1 April 2024 - Approval of first in class, oral, Factor D inhibitor based on results from pivotal ALPHA Phase ...

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