NOVARTIS

NOVARTIS logo
🇨🇭Switzerland
Ownership
Public, Private
Established
1996-01-01
Employees
76K
Market Cap
$242.6B
Website
https://www.novartis.com/our-science/novartis-institutes-biomedical-research
cen.acs.org
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Rewriting the health-care script in Africa

Kelly Chibale, from a Zambian village to Cambridge and Scripps, founded the Holistic Drug Discovery and Development Centre (H3D) at the University of Cape Town in 2010. H3D, supported by research and funding partners, focuses on malaria, tuberculosis, and antibiotic-resistant diseases, developing MMV390048, the first small-molecule clinical candidate discovered by an Africa-led team. Chibale emphasizes the need for global recognition and collaboration with African scientists to address diverse health challenges and foster innovation.
thirdeyenews.in
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Renal Cell Carcinoma Clinical Trial Pipeline Market | Application, Size, Share Analysis 2024-2031

The Renal Cell Carcinoma Clinical Trial Pipeline Market is projected to grow significantly from 2024 to 2031, driven by technological innovations, rising demand, and regulatory changes. The market is segmented by type and application, with key players including Amgen, AstraZeneca, and Pfizer. Clinical trials focus on novel therapies, drug combinations, and targeted treatments, aiming to improve outcomes for renal cell carcinoma patients.
investopedia.com
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Novartis Breast Cancer Drug Found To Cut Disease Recurrence

Novartis' Kisqali, combined with endocrine therapy, reduced breast cancer recurrence risk by 28.5% beyond the three-year treatment period. The company expects an FDA decision on approval this quarter.
cnbc.com
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Drugmakers bet billions that targeted radiation could become the next cancer breakthrough

Drugmakers like Bristol Myers Squibb, AstraZeneca, and Eli Lilly invest billions in radiopharmaceuticals, which deliver radiation directly to tumors. These drugs, in development for various cancers, attach radioactive material to targeting molecules, sparing healthy cells. Novartis' successes with Lutathera and Pluvicto have spurred interest, but manufacturing and logistics remain complex. The market potential ranges from $5 billion to tens of billions, depending on efficacy across cancer types.
globenewswire.com
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Cell-Free DNA Isolation and Extraction Market 2024: Growing

The cell-free DNA isolation and extraction market is projected to grow from $1.81 billion in 2023 to $2.49 billion by 2028, driven by increasing cancer prevalence, advancements in genomics, and demand for personalized medicine. Key trends include product innovation, strategic partnerships, and technological advancements in DNA extraction techniques.
sdbj.com
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Novartis Plans $40M Facility in Carlsbad

Novartis invests over $200 million in a new 10,000 sq ft radiotherapy facility in Carlsbad, creating 30+ jobs. The facility focuses on radioligand therapy manufacturing, aiming to improve cancer treatment precision. This marks Novartis' first U.S. manufacturing facility in California.
whatech.com
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Global Statins Market Insights Discussed Regarding Key Insights and Leading Countries

The statins market, valued at $22B, is projected to reach $15B by 2021, driven by cardiovascular disease prevalence, cholesterol management awareness, and statin formulation advancements. Challenges include generic competition, alternative therapies, and side effects. Opportunities lie in combination therapies and emerging markets.
novartis.com
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Novartis Kisqali® shows deepening benefit in new analysis, reducing the risk of recurrence ...

Kisqali (ribociclib) + endocrine therapy (ET) reduces recurrence risk by 28.5% beyond 3 years in HR+/HER2- early breast cancer, with consistent iDFS benefits across subgroups, including node-negative disease. Safety aligns with prior findings, and FDA action is expected in Q3.
globenewswire.com
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Novartis Kisqali® shows deepening benefit in new analysis

Kisqali (ribociclib) + endocrine therapy (ET) reduces recurrence risk by 28.5% beyond 3 years in HR+/HER2- early breast cancer, with consistent benefits across subgroups, including node-negative disease. Safety remains consistent with low-grade adverse events. Results to be presented at ESMO; FDA action expected in Q3.
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