Foundation for Biomedical Research and Innovation (FBRI) in Kobe, Japan becomes first CAR-T cell therapy commercial manufacturing site in Asia
Novartis global CAR-T manufacturing footprint now spans four continents, bringing Kymriah closer to patients and healthcare professionals around the world
Prestigious FBRI is recognized for its world-class expertise and established practice in CAR-T cell therapy
Global CAR-T manufacturing growth includes recent FDA approval for further capacity expansion in the US, …
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Latest data show Cosentyx® provides fast and strong skin clearance, significant improvement in quality of life and a favorable safety profile1,2
Moderate-to-severe psoriasis affects more than 350,000 children worldwide3, with the physical and psychological burden disrupting important formative years4
FDA has accepted a submission for Cosentyx in moderate-to-severe plaque psoriasis in children and adolescents aged 6 to <18 years
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Acquisition expands the Novartis footprint in ophthalmology and enhances the company’s position as an AAV-based gene therapy powerhouse.
Novartis gains two pre-clinical optogenetic AAV gene therapy programs and novel delivery technology for treating inherited retinal dystrophies and geographic atrophy.
Inherited retinal dystrophies, including advanced retinitis pigmentosa, affect greater than 2 million patients worldwide, and geographic atrophy affects approximately 5 million patients worldwide.
Novartis has been granted an option to in-license global rights of MP0420 and MP0423 – multi-targeted direct acting antiviral therapeutic candidates demonstrating potential efficacy against COVID-19
MP0420 and MP0423 are potential medicines with a unique approach for both the prevention and treatment of COVID-19, with the possibility to manufacture at scale, easy administration and with the potential to bypass cold storage
Switzerland based Molecular Partners, a global leader in the development of DARPin …
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Q3 net sales from continuing operations1were in line with prior year (cc2, +1% USD):
Growth drivers included Entresto USD 632 million (+45% cc), Zolgensma USD 291 million (+79% cc), Cosentyx USD 1 012 million (+7% cc), Kisqali USD 183 million (+50% cc) and Promacta/Revolade USD 442 million (+16% cc)
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C3 glomerulopathy (C3G) is a rare renal disease, affecting young patients with a poor prognosis and significant unmet need.1–3
Iptacopan (LNP023) is a potential first-in-class, oral, potent and selective factor B inhibitor of the complement system’s alternative pathway, targeting the underlying cause of C3G.4–6
Data presented at the American Society of Nephrology (ASN) 2020 Annual Meeting shows that investigational iptacopan …
Orphan drug designation isreserved for medicines treating rare, life-threatening or chronically debilitating diseases
IgA nephropathy(IgAN), while rare,is the most common form ofglomerulonephritis, affectingmostly young adults with no approved treatment option and significant risk to progress to e …
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Orphan drug designation isreserved for medicines treating rare, life-threatening or chronically debilitating diseases
IgA nephropathy(IgAN), while rare,is the most common form ofglomerulonephritis, affectingmostly young adults with no approved treatment option and significant risk to progress to e …
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Orphan drug designation isreserved for medicines treating rare, life-threatening or chronically debilitating diseases
IgA nephropathy(IgAN), while rare,is the most common form ofglomerulonephritis, affectingmostly young adults with no approved treatment option and significant risk to progress to e …
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