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

Treating meibomian gland dysfunction and glaucoma

80% of glaucoma patients on prostaglandin analogs (PGAs) have Grade 2-3 meibomian gland dysfunction (MGD), worsening ocular surface disease (OSD). Benzalkonium chloride (BAK) in chronic drops disrupts tear film stability. Symptoms like redness and tearing can lead to poor medication compliance and glaucoma progression. Innovative non-preserved or non-BAK glaucoma medications, sustained-release drug delivery systems, and non-drug treatments like selective laser trabeculoplasty (SLT) or minimally invasive glaucoma surgeries (MIGS) offer solutions. Preservative-free drops and procedural interventions aim to mitigate MGD and OSD effects.
finance.yahoo.com
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Legend Biotech Corporation (LEGN): Among Hedge Funds' Top Biotech Stock Picks

Legend Biotech Corporation (NASDAQ:LEGN) ranks 10th among hedge funds' top biotech stock picks, with 24 hedge fund investors and RA Capital's $332 million stake. LEGN, a commercial-stage biotech developing cancer treatments, focuses on its Carvytki drug for myeloma, which saw $186 million in Q2 sales, a 19% sequential growth.
healio.com
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Data support pembrolizumab regimen as 'new standard' for advanced cervical cancer

Pembrolizumab plus chemoradiotherapy significantly improved OS for women with high-risk locally advanced cervical cancer, making it the new standard of care.
theglobeandmail.com
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Where Will Merck Stock Be in 5 Years?

Merck's stock has risen 72% in 5 years, driven by Keytruda's success, but faces uncertainty as Keytruda's patent expires in 2028. Merck forecasts 2024 revenue growth of 5-7% and seeks new blockbusters, while competition from biosimilars and alternative treatments poses risks.
ajmc.com
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Experts Highlight New Dermatological Treatments, Importance of Clinical Trial Diversity

Experts at the Skin of Color Update discussed recent FDA approvals for dermatology treatments, emphasizing the importance of clinical trial diversity. Key approvals included roflumilast and tapinarof for psoriasis, roflumilast for seborrheic dermatitis, and roflumilast for atopic dermatitis. Additionally, biologic therapies such as bimekizumab for psoriasis, secukinumab for hidradenitis suppurativa, and nemolizumab for prurigo nodularis were highlighted. The FDA is developing a diversity action plan to ensure more inclusive clinical trials.
nature.com
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Datopotamab–deruxtecan plus durvalumab in early-stage breast cancer

R.A.S., M.S.T., C.Y., R.N., H.S.R., M.D., A.J.C., E.S.-R., J.C.B., C.O., K.K., A.D.E., C.V., N.W., K.S.A., A.S.C., C.F., C.I., A.T., J.T., K.Y., L.H., K.G., F.M.H., T.S., A.L.A., P.B., P.N., G.L.H., W.F.S., J.P., P.P., A.D.M., D.Y., L.J.v.V., N.M.H., L.J.E. report various institutional research funding, advisory roles, consultancy, honoraria, patents, and stock ownership.
prnewswire.com
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Experts ensure that early detection and proper prevention are key to tackling the future

MEDSIR hosted an informational breakfast at the ESMO congress in Barcelona, bringing together key players in cancer research to discuss the future of breast and lung cancer treatments, emphasizing the importance of early detection, international collaboration, and the integration of AI and new technologies.
yahoo.com
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US FDA approves injectable version of Roche's multiple sclerosis therapy

The FDA approved Roche's Ocrevus Zunovo, an under-the-skin injection for multiple sclerosis, expanding treatment options to centers unable to administer the IV version. The 10-minute injection, given twice a year, targets CD20-positive B cells and is based on a study showing no significant difference in Ocrevus levels when administered subcutaneously.
aacrjournals.org
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CSF1R Inhibition in Patients with Advanced Solid Tumors or Tenosynovial Giant Cell Tumor

Various researchers report financial relationships with pharmaceutical companies, including Deciphera, during and outside the conduct of the study.
biopharmadive.com
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Subcutaneous Tecentriq gets FDA OK; Gilead shot succeeds in second HIV trial

Roche's subcutaneous Tecentriq approved for cancer treatment; Gilead's twice-yearly HIV shot reduces infection risk by 96%; Biogen appoints Lloyd Minor and Menelas Pangalos as independent directors; Sanofi secures rights to a rare cancer radiopharmaceutical; Eli Lilly to expand Irish manufacturing for Alzheimer's drug Kisunla.
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