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News about "Jazz Pharmaceuticals "
US FDA Approves Ziihera for First-Line HER2+ Gastroesophageal Cancer
The US Food and Drug Administration (FDA) approves Ziihera plus tislelizumab and chemotherapy for first-line treatment of HER2+ advanced gastroesophageal adenocarcinoma regardless of PD-L1 status.
Jazz Pharmaceuticals | 26/08/2026 | By News Bureau
Jazz Pharmaceuticals has agreed to acquire Actio Biosciences for USD 820 million upfront and up to USD 500 million in contingent payments, expanding its rare epilepsy pipeline with investigational therapy ABS-1230.
Jazz Pharmaceuticals | 12/08/2026 | By News Bureau
U.S. Food and Drug Administration accepts sBLA for Ziihera with Priority Review, backed by Phase III data showing improved outcomes in HER2-positive advanced gastric and gastroesophageal cancers.
Jazz Pharmaceuticals | 29/04/2026 | By News Bureau | 199
Jazz and Saniona Enter Global License Deal for Preclinical Epilepsy Candidate SAN2355
Jazz Pharmaceuticals and Saniona have entered into a global licensing agreement, giving Jazz exclusive worldwide rights to develop and commercialise SAN2355, a highly selective Kv7.2/Kv7.3 activator currently in preclinical development for epilepsy and other neurological conditions. <br />
Jazz Pharmaceuticals | 21/08/2025 | By Dineshwori | 321
The US Food and Drug Administration (FDA) has granted accelerated approval for Jazz Pharmaceuticals' Modeyso (dordaviprone) for the treatment of adult and pediatric patients 1 year of age and older with H3 K27M-mutant diffuse midline glioma – a rare and highly aggressive brain tumour – with progressive disease following prior therapy.
Jazz Pharmaceuticals | 08/08/2025 | By Dineshwori | 577
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