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Sanofi

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Sanofi shelves mRNA seasonal flu effort, pivots to proven vaccines
business1 month ago

Sanofi shelves mRNA seasonal flu effort, pivots to proven vaccines

Sanofi has deprioritized its phase 1 mRNA seasonal flu program, scrapping the effort as part of a broader strategic shift, while continuing to pursue an mRNA vaccine for an H5 pandemic and focusing on established influenza vaccines (Fluzone High-Dose, Flublok). The influenza/COVID vaccine franchise generated €2.3 billion last year, a 6% decline from 2024 amid lower US immunization rates, and the company underscored a multi‑platform vaccine strategy, including the Dynavax acquisition, as its growth path.

FDA slows two fast-track drug reviews amid safety flags in voucher plan
health1 month ago

FDA slows two fast-track drug reviews amid safety flags in voucher plan

Reuters reports the U.S. FDA has delayed reviews of two drugs selected for the National Priority Voucher fast-track program after agency scientists flagged safety and efficacy concerns, including a treatment-related death linked to one drug. Disc Medicine's experimental therapy for a rare blood disorder was pushed back due to questions about trial data and abuse risk, while Sanofi's Tzield for late-stage type 1 diabetes was delayed over adverse events, including seizures and a death. Two other program drugs—Boehringer Ingelheim's zongertinib and Lilly's weight-loss pill—were also delayed by weeks. The delays underscore the program’s aim to accelerate reviews only when warranted by robust safety/efficacy data, amid ongoing scrutiny of how political factors may influence drug decisions.

Sanofi's $2.2 Billion Acquisition of Dynavax Boosts Vaccine Portfolio
business2 months ago

Sanofi's $2.2 Billion Acquisition of Dynavax Boosts Vaccine Portfolio

Sanofi is acquiring U.S. biotech Dynavax for $2.2 billion to expand its adult vaccine portfolio, including hepatitis B and shingles vaccines, aiming to diversify and boost revenue growth amid regulatory and market pressures. The deal, expected to close in early 2026, also includes an experimental shingles vaccine with potential long-term sales, while Sanofi faces setbacks with an FDA rejection of its multiple sclerosis drug.

European Markets Reach New Highs Amid Pharma Gains and Economic Growth
business2 months ago

European Markets Reach New Highs Amid Pharma Gains and Economic Growth

European markets closed mixed with Novo Nordisk shares jumping 9.2% after FDA approval for a GLP-1 pill, while Sanofi announced a $2.2 billion acquisition. Gold and silver futures hit new highs, and U.S. visa bans were imposed on EU officials involved in social media censorship. Asia-Pacific markets traded mostly higher, and U.S. futures remained flat despite record closes for the S&P 500.

Apogee's Eczema Drug Shows Promising Results, Challenging Industry Leaders
healthcare7 months ago

Apogee's Eczema Drug Shows Promising Results, Challenging Industry Leaders

Apogee Therapeutics' promising eczema drug showed strong efficacy in Phase 2 trials, outperforming rivals like Sanofi's Dupixent, but its shares fell sharply after the announcement. The drug could potentially rival Sanofi's top revenue-generating treatments if further trials succeed, with plans for Phase 3 testing in 2026.

Sanofi's Rilzabrutinib Shows Promise in Treating Rare Platelet Disorder
health1 year ago

Sanofi's Rilzabrutinib Shows Promise in Treating Rare Platelet Disorder

Sanofi's rilzabrutinib, an oral treatment for immune thrombocytopenia (ITP), showed promising results in a Phase 3 trial, improving platelet response and reducing bleeding episodes. The drug, a bruton's kinase inhibitor, is safer and better tolerated than existing treatments, potentially setting a new standard for ITP therapy. Meanwhile, Novo Nordisk's etavopivat reduced severe pain crises in sickle cell disease patients in a Phase 2 study, though results were not statistically significant. Beam Therapeutics' CRISPR-based therapy for sickle cell disease also showed consistent positive results, with no severe pain crises reported among treated patients.

"GLP-1 Diabetes Drug Slows Parkinson's Progression in Small Trial"
health-medical-research1 year ago

"GLP-1 Diabetes Drug Slows Parkinson's Progression in Small Trial"

A small mid-stage trial has shown that the diabetes drug lixisenatide, similar to Ozempic, helped slow the progression of motor disability in patients with early-stage Parkinson's disease. The drug, made by Sanofi, demonstrated potential in mitigating symptoms such as tremors and stiffness, but was also associated with an increased risk of gastrointestinal side effects. Larger and longer studies are needed to fully determine the efficacy and safety of this treatment for Parkinson's disease.

Sanofi Settles Thousands of Zantac Cancer Lawsuits in US
legalpharmaceuticals1 year ago

Sanofi Settles Thousands of Zantac Cancer Lawsuits in US

Sanofi has reached an agreement in principle to settle 4,000 U.S. lawsuits linking the discontinued heartburn drug Zantac to cancer, without disclosing the financial terms. The settlement, which still needs to be finalized, will resolve most of the lawsuits against the French pharmaceutical company in U.S. state courts, except for Delaware. Sanofi did not admit any liability in the settlement and stated that it is settling to avoid the expense and ongoing distraction of the litigation. The company still faces about 20,000 lawsuits over Zantac in Delaware state court, and a judge is considering the fate of approximately 70,000 cases filed against Sanofi and other defendants.

Sanofi and AstraZeneca's RSV Antibody Faces Limited Supply Amid High Demand
healthcare2 years ago

Sanofi and AstraZeneca's RSV Antibody Faces Limited Supply Amid High Demand

Sanofi anticipates limited supply of its infant RSV antibody Beyfortus, co-developed with AstraZeneca, in the first quarter of this year due to overwhelming demand, with plans to boost production but uncertainty about the extent of progress that can be made in 2024. CEO Paul Hudson highlighted efforts to address manufacturing bottlenecks and increase capacity to tackle supply constraints.

Sanofi's $2.2 Billion Acquisition of Inhibrx for Rare-Disease Drug
business2 years ago

Sanofi's $2.2 Billion Acquisition of Inhibrx for Rare-Disease Drug

French healthcare company Sanofi has agreed to acquire U.S. biotech firm Inhibrx for up to $2.2 billion, gaining access to the experimental drug INBRX-101 designed to treat Alpha-1 Antitrypsin Deficiency. The deal includes spinning off Inhibrx's other experimental drugs into a separate company, with Sanofi retaining an 8% stake, and Inhibrx shareholders receiving $30 per share in cash plus shares in the spun-off company. This acquisition aligns with Sanofi's strategy to focus on differentiated and potential best-in-class products, reinforcing its rare disease portfolio.

Sanofi's $2.2B Acquisition of Inhibrx Strengthens Drug Pipeline
business-healthcare2 years ago

Sanofi's $2.2B Acquisition of Inhibrx Strengthens Drug Pipeline

Sanofi is acquiring California-based biotech company Inhibrx for up to $2.2 billion to bolster its pipeline of inflammation-targeting drugs, with a focus on Inhibrx’s experimental therapy for AATD, a disease affecting the lungs and liver. Inhibrx's other drug candidates, including cancer-targeting immunotherapies, will be part of a new company led by Inhibrx's founder and CEO.