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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Huntington’s disease is a rare, inherited neurodegenerative disease that leads to progressive disability and death
There are no approved disease modifying therapies that delay disease onset or slow progression of the disease
Branaplam (LMI070) is an orally administered, small molecule RNA splicing modulator that could potentially reduce the levels of mutant huntingtin protein
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If approved, inclisiran will be the first and only small interfering RNA(siRNA) in Europe for patients with hypercholesterolemia or mixed dyslipidemia1
Cardiovascular disease (CVD) claims 3.9 million lives annually in Europe2,and 80% of high-risk patients do not reach guideline-recommended low-density lipoprotein cholesterol (LDL-C) targets despite the widespread …
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