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$REGN

41 articles found
24 positive
3 negative
14 neutral
The Motley FoolThe Motley Fool··Prosper Junior Bakiny

Can Eli Lilly Become First $2T Healthcare Giant? Three Growth Catalysts in Focus

Eli Lilly eyes $2 trillion valuation from weight-loss drugs, Alzheimer's breakthroughs, and AI-powered R&D following recent market pullback.
PFENVDALLYREGNhealthcare stocksweight loss drugs
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

Hemophilia Treatment Revolution: 50+ Companies Race to Transform Patient Care

Over 50 drugmakers advance 55+ hemophilia treatments as Novo Nordisk and competitors pursue gene therapies and next-gen factors.
NVORHHBYREGNBAYRYMGXclinical trialsgene therapy
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

Complement Inhibitors Market Set for Robust Growth Through 2036 as C5, C3 Therapies Expand

Complement inhibitors market projected for strong growth through 2036, driven by rising disease prevalence and C5/C3-targeted drug approvals across multiple indications.
NVSSNYRHHBYAZNREGN+3clinical trialsmarket growth
BenzingaBenzinga··Piero Cingari

Oil Rallies 6% on Iran Tensions as Fed Holds Steady; Tech Earnings in Focus

Oil surges 5-6% on Iran tensions; Treasury yields top 4.4%. Fed holds rates at 3.75% as tech stocks fall 1-2% on OpenAI revenue miss.
METAMSFTAMZNGOOGGOOGL+14Federal Reservehyperscalers
GlobeNewswire Inc.GlobeNewswire Inc.··Not Specified

Intellia Therapeutics Raises $180M in Stock Offering to Fuel CRISPR Pipeline

Intellia Therapeutics raises $180M via stock offering at $10.75/share to advance CRISPR gene-editing therapies, with lead underwriters Jefferies, Goldman Sachs, Citigroup.
REGNNTLApublic offeringcapital raise
BenzingaBenzinga··Vandana Singh

Regeneron Strikes Landmark Deal With Trump Administration on Drug Pricing

Regeneron agrees with Trump Administration to lower drug prices via Medicaid benchmarking and free gene therapy access, receiving three years of tariff relief and regulatory certainty.
REGNFDA approvalgene therapy
GlobeNewswire Inc.GlobeNewswire Inc.··Fda

FDA Approves Regeneron's Landmark Gene Therapy for Genetic Hearing Loss in Record 61 Days

FDA approves $REGN's Otarmeni, first dual AAV gene therapy for genetic hearing loss, in record 61 days under priority voucher program. 80% of patients showed improved hearing.
REGNFDA approvalrare disease
GlobeNewswire Inc.GlobeNewswire Inc.··Na

Regeneron Strikes Historic Deal with U.S. Government on Drug Pricing

Regeneron offers gene therapy Otarmeni free and Praluent at lower pricing in exchange for tariff relief and exemption from future pricing mandates.
REGNgene therapytariff relief
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

65+ Pharma Giants Race to Dominate COPD Market with Next-Gen Biologics

Over 65 pharma companies advance 75+ COPD drugs, shifting from traditional bronchodilators to targeted biologics as AstraZeneca's tozorakimab validates new approaches.
AMGNPFESNYAZNUPB+2clinical trialsbiologics
BenzingaBenzinga··Vandana Singh

Sanofi Beats Earnings as Dupixent Expansion Into Pediatric Urticaria Broadens Growth

Sanofi's Dupixent gains FDA approval for pediatric urticaria as Q1 earnings beat expectations with 30.8% drug growth at $12.31B sales.
SNYREGNchronic spontaneous urticariaFDA approval
GlobeNewswire Inc.GlobeNewswire Inc.··Sanofi And Regeneron

Dupixent Wins FDA Nod for Young Children With Chronic Urticaria, Expanding Market Reach

FDA approves Dupixent for children ages 2-11 with uncontrolled chronic spontaneous urticaria, marking first biologic treatment for this pediatric population.
SNYREGNchronic spontaneous urticariaFDA approval
GlobeNewswire Inc.GlobeNewswire Inc.··Sanofi And Regeneron

Sanofi and Regeneron Win FDA Nod for Dupixent in Young Children With Chronic Urticaria

FDA approves Dupixent for children ages 2-11 with chronic spontaneous urticaria, marking first biologic treatment for this pediatric population.
SNYREGNchronic spontaneous urticariaFDA approval
GlobeNewswire Inc.GlobeNewswire Inc.··Researchandmarkets.Com

Bispecific Antibodies Poised for $60B Market by 2031 as 550+ Trials Reshape Therapeutics

Bispecific antibody market projected to reach $60 billion by 2031 from $16 billion in 2025, with 550+ clinical trials and 18 approved drugs driving sector transformation.
AMGNJNJPFEABBVRHHBY+3clinical trialsautoimmune diseases
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

Lung Cancer Drug Race Heats Up: 100+ Companies Pursue NSCLC Breakthroughs

Over 100 pharmaceutical companies compete to develop 120+ NSCLC pipeline drugs, with 30+ in late-stage trials. Precision oncology advances drive innovation in biomarker-selected populations.
JNJMRKPFEABBVLLY+6FDA approvalclinical trials
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

Myasthenia Gravis Market Poised for Transformation With 8 Late-Stage Drug Candidates

Generalized myasthenia gravis market valued at $5.9B in 2025, projected to grow 9.1% annually through 2036 as eight promising late-stage therapies advance.
NVSAZNREGNMKKGYROIV+3clinical trialsautoimmune disease
GlobeNewswire Inc.GlobeNewswire Inc.··Delveinsight

US Eosinophilic Esophagitis Market Poised for Explosive Growth as Novel Drug Classes Emerge

US eosinophilic esophagitis market valued at $647M in 2025 projected to grow 13.2% annually through 2036, driven by novel drug classes and improved diagnostics.
AMGNSNYAZNREGNEPRX+3market growthpharmaceutical pipeline
GlobeNewswire Inc.GlobeNewswire Inc.··Not Specified

Neomorph Raises $100M Series B to Accelerate Molecular Glue Degrader Pipeline

Neomorph closes $100M Series B led by Deerfield Management to advance NEO-811, its molecular glue degrader for kidney cancer, and expand its pipeline.
REGNclinical trialbiotechnology
BenzingaBenzinga··Vandana Singh

Telix Pharma Surges on $2.14B Regeneron Deal for Solid Tumor Radiotherapies

Telix Pharma secures $2.14B partnership with Regeneron for solid tumor radiopharmaceuticals while reporting 11% quarterly revenue growth and FDA acceptance of brain cancer imaging application.
TLXREGNFDA approvalsolid tumors
GlobeNewswire Inc.GlobeNewswire Inc.··Sanofi/Regeneron

Sanofi, Regeneron Win EU Approval for Dupixent in Pediatric Chronic Urticaria

Sanofi and Regeneron win EU approval for Dupixent as first targeted therapy for chronic urticaria in children ages 2-11, expanding the blockbuster drug's market reach.
SNYREGNDupixentdupilumab
GlobeNewswire Inc.GlobeNewswire Inc.··Sanofi And Regeneron

Sanofi, Regeneron Win EU Nod for Dupixent in Young Children with Chronic Urticaria

Dupixent gains European approval for treating moderate-to-severe chronic spontaneous urticaria in children ages 2-11, expanding the drug's pediatric portfolio.
SNYREGNchronic spontaneous urticariaDupixent