MedPath

BAYER AG

BAYER AG logo
🇩🇪Germany
Ownership
Public
Established
1863-08-01
Employees
99.7K
Market Cap
$30.1B
Website
http://www.bayer.com
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.
media.market.us
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Agricultural Biotechnology Market Hits $232 Billion By 2033

The agricultural biotechnology market is projected to grow from USD 111 billion in 2023 to USD 232 billion by 2033, driven by advancements in technology and sustainable practices. Innovations like biofertilizers, biopesticides, and genetic enhancements improve yields and reduce environmental impact. Key players include Corteva, BASF, and Bayer AG, with strategic developments focusing on gene editing and regenerative agriculture. The market faces challenges such as high costs and environmental concerns, but is essential for meeting global food demands.
openpr.com
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Hemophilia B Clinical Trials 2024: EMA, PDMA, FDA Approvals

DelveInsight's 'Hemophilia B Pipeline Insight, 2024' report details the global Hemophilia B treatment market, including clinical trials, therapies, and company developments. Key companies and therapies in various stages of development are highlighted, along with market drivers and barriers.
openpr.com
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Adrenoleukodystrophy Clinical Trials 2024: EMA, PDMA, FDA

DelveInsight's 'Adrenoleukodystrophy Pipeline Insight, 2024' report details 11+ treatment therapies by 10+ companies, including Autobahn Therapeutics, Viking Therapeutics, and SwanBio Therapeutics. Emerging therapies like ABX-002, VK0214, and SBT101 are expected to impact the market. Minoryx Therapeutics plans to re-examine Nezglyal's approval after CHMP's refusal.
pmc.ncbi.nlm.nih.gov
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Artificial intelligence as a tool in drug discovery

AI revolutionizes drug discovery by enhancing efficiency and accuracy in identifying drug candidates and predicting pharmacological properties. It integrates machine learning and deep learning to optimize decision-making and accelerate drug design, despite challenges like data privacy and model interpretability. AI's potential in uncovering therapeutic targets and repurposing drugs is significant, with applications in target identification, lead optimization, and predictive modeling.
genengnews.com
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The Great Pharma Wasteland

Pharmaceutical industry inefficiencies stem from high costs per drug approval, frequent C-level executive changes, and strategic R&D restructuring unrelated to science. AI-drug discovery companies should commit to programs until Phase I completion to avoid waste and maximize patient benefit.
medcitynews.com
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Organon Gets More Skin in the Game by Acquiring Roivant's Dermatology Subsidiary

Organon plans to acquire Dermavant for up to $1.2 billion, gaining its commercialized plaque psoriasis drug Vtama, which is under FDA review for atopic dermatitis. Vtama sales grew to $75.1 million in FY2023, but face competition in a crowded market. Organon aims to leverage its global scale to expand Vtama's reach.
prweek.com
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Brands2Life launches pharma tech offer with MHP hire

Brands2Life appoints Isabelle Scali as head of pharma to lead new service aiding pharmaceutical companies in navigating health and technology, aiming for more agile and creative healthcare communications.
medpagetoday.com
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Survival Win for Pembrolizumab in Early Triple-Negative Breast Cancer

PD-1 inhibition with pembrolizumab before and after surgery significantly improves 5-year overall survival (86.6% vs 81.7%) in high-risk early triple-negative breast cancer, according to KEYNOTE-522 trial results.
pharmabiz.com
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Phase III ARANOTE trial of darolutamide plus ADT significantly reduced the risk

Darolutamide plus ADT significantly reduced the risk of radiological progression or death by 46% in patients with metastatic hormone-sensitive prostate cancer (mHSPC), with consistent benefits across subgroups. Treatment emergent adverse events were low and similar between groups. The ARANOTE trial results were presented at the 2024 ESMO Congress and published in The Journal of Clinical Oncology, supporting the potential of darolutamide as a foundational therapy in prostate cancer.
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