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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
fintechmagazine.com
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Novartis

Novartis, a Swiss global healthcare company with 79,000 employees, focuses on innovative pharmaceutical solutions, led by CEO Vasant Narasimhan. The company's diverse portfolio includes pharmaceuticals, generics, and eye care, leveraging biotechnology for treatments. Novartis invests in clinical trials and patient support, committed to pioneering new treatments through robust R&D.

Opthea Limited announces key executive leadership changes and senior hires

Opthea Limited has made executive leadership changes in finance and commercial areas, and hired senior staff in biometrics, clinical operations, and market access. These changes are in preparation for the anticipated clinical trial data in 2025. Key hires include Dan Geffken as interim CFO, Mike Campbell as CCO, Dayong Li as SVP of Biometrics, Jen Watts as VP of Global Clinical Operations, and Anthony Bonifazio as VP of Market Access.
springermedizin.de
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Relacorilant or surgery improved hemostatic markers in Cushing syndrome

Glucocorticoid-induced hypercoagulopathy in endogenous Cushing syndrome (CS) increases thromboembolic risk, with CS patients having an 18-fold higher risk of venous thromboembolism (VTE) compared to the general population. VTE risk is highest postoperatively, with up to 5.6% incidence. Hypercoagulopathy persists post-surgery and improves within 6 months. Relacorilant, a selective glucocorticoid receptor modulator, showed improvements in coagulation markers without undesirable effects, suggesting potential benefits for CS patients, particularly those at high VTE risk.
neurologylive.com
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End-of-Dose Phenomena Observed With Multiple Sclerosis Medication Ofatumumab

34% of 103 MS patients on ofatumumab experienced end-of-dose phenomena, linked to higher disability, longer disease duration, and older age. Ofatumumab showed lower odds of wearing-off effect vs. ocrelizumab and higher persistence rates compared to other DMTs.
oncnursingnews.com
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Neoadjuvant Dato-DXd, Durvalumab Response Rates Vary in Breast Cancer

Dato-DXd plus durvalumab achieved a 50% pathologic complete response (pCR) rate in stage II/III high-risk HER2-negative breast cancer patients, according to the I-SPY 2.2 trial. The study emphasizes evaluating treatment response per response predictive subtype (RPS) and suggests further investigation in immune-positive and hormone receptor (HR)-negative/DNA damage repair deficiency (DRD)-negative subtypes. The combination's efficacy was supported by the BEGONIA trial, showing a 79% objective response rate in metastatic triple-negative breast cancer. The I-SPY 2.2 trial design uses RPS to optimize drug assignment, aiming to improve efficacy and minimize toxicity.
dataintelo.com
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Type 1 Diabetes (T1D) Market Research Report 2032

The global Type 1 Diabetes (T1D) market, valued at $6.5 billion in 2023, is projected to grow to $11.3 billion by 2032, driven by increasing diabetes prevalence, technological advancements, and rising healthcare expenditure. Innovations like CGM systems and artificial pancreas devices enhance patient outcomes. Insulin therapy remains central, with advancements in delivery methods and digital health integration. Regional growth is led by North America, with Asia Pacific showing rapid expansion. Challenges include treatment costs and access, with efforts underway to improve affordability and equity.
economica.ma
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Personalized Precision Medicine Market Share | 2031 Forecast

The global Personalized Precision Medicine Market report offers detailed segmentation and strategic guidance, covering manufacturers, regions, product categories, and applications. Key insights include market evolution, current conditions, future projections, and analysis of key players like Agilent Technologies, Biogen, Johnson & Johnson, and Novartis. The report aids stakeholders in navigating market dynamics and capitalizing on opportunities.
finance.yahoo.com
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Pharma Stock Roundup: FDA Approvals for LLY, MRK, AZN & JNJ Drugs

FDA approves Eli Lilly’s Ebglyss for eczema, Novartis’ Kisqali for early breast cancer, Merck’s Keytruda for malignant pleural mesothelioma, J&J’s Rybrevant for advanced lung cancer, and AstraZeneca’s Fasenra for eosinophilic granulomatosis with polyangiitis.

Biotechs investigate ways to adapt to new clinical trial regulation and economic flux

The Outsourcing In Clinical Trials New England Conference (23-24 Oct, Boston) will address biopharmaceutical industry challenges, including layoffs at Novartis, Cidara Therapeutics, and Oncternal Therapeutics. Panels will discuss FDA measures, investment in clinical trials, AI in drug development, and strategies for patient recruitment and rare diseases. Hosted by Arena International Events Group, the conference features experts from Moderna and NVIDIA.
mmm-online.com
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Rx Rundown: MaxCyte, Roche, and more

MaxCyte partners with Kamau Therapeutics, Arvato Systems with Advanco, Revance Therapeutics' acquisition impacted by Crown Laboratories, Lifebit and CanPath strategic partnership, Kajeet and Avery Telehealth partnership. FDA approves Apple's sleep apnea detection, Roche's Ocrevus injectable, Novartis Kisqali, Lilly's EBGLYSS, issues alert on Astellas' Veozah, clears Eversense CGM system. Nura Bio raises $68 million, Arzeda $38 million. Cigna's Express Scripts sues FTC, Burson launches Decipher Health, short interest in healthcare stocks rises, Hill Holliday's Quest, Ascendis Pharma's positive Phase 3 results, WHO approves Bavarian Nordic's mpox vaccine, J&J's talc verdict overturned, Prime Therapeutics' new vision, Blue Matter acquires Sam Brown Inc.
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