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Press Release: Dupixent late-breaking data from NOTUS confirmatory phase 3 COPD study presented at ATS and published in NEJM

Press Release: Dupixent late-breaking data from NOTUS confirmatory phase 3 COPD study presented at ATS and published in NEJM
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Sanofi: Dupixent® late-breaking data from NOTUS confirmatory phase 3 COPD study presented at ATS and published in NEJM

Dupixent® late-breaking data from NOTUS confirmatory phase 3 COPD study presented at ATS and published in NEJM NOTUS results confirm landmark data from the phase 3 BOREAS study and show Dupixent significantly ....

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Press Release: Dupixent® Late-Breaking Data From NOTUS Confirmatory Phase 3 COPD Study Presented At ATS And Published In NEJM

Press Release: Dupixent® Late-Breaking Data From NOTUS Confirmatory Phase 3 COPD Study Presented At ATS And Published In NEJM
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United States , France General , Tarik Elgoutni , Thomas Kudsk Larsen , Felix Lauscher , Timothy Gilbert , Nathalie Pham , Surya Bhatt , Evan Berland , Hanna Hodge , Corentine Driancourt , Vesna Tosic , Clinical Research Program , Regeneron Pharmaceuticals Inc , American Thoracic Society , Division Of Pulmonary , European Union , Us Department Of Justice , Dupilumab Development Program , Drug Administration , Exchange Commission , University Of Alabama At Birmingham , International Conference , Regeneron Genetics Center , Thoracic Society , New England Journal ,

Press Release: Dupixent® sBLA accepted for FDA Priority Review for treatment of COPD with type 2 inflammation -February 23, 2024 at 01:01 am EST

Dupixent® sBLA accepted for FDA Priority Review for treatment of COPD with type 2 inflammation Priority Review granted based on positive results from two Phase 3 trialsIf approved,. ....

France General , Felix Lauscher , Evan Berland , Corentine Driancourt , Vesna Tosic , Tarik Elgoutni , Timothy Gilbert , Nathalie Pham , Eva Schaefer Jansen , Hannah Kwagh , Sally Bain , Drug Administration , Dupilumab Development Program , Regeneron Genetics Center , Regeneron Pharmaceuticals Inc , Exchange Commission , Clinical Research Program , European Union , Priority Review , Biologics License Application , Private Securities Litigation Reform Act , Statement Regarding Forward Looking , Forward Looking Statements , Digital Media , Regeneron Pharmaceuticals , Product Candidates ,

Dupixent® (dupilumab) sBLA Accepted for FDA Priority Review for Treatment of COPD with Type 2 Inflammation

Priority Review granted based on positive results from two Phase 3 trials; if approved, Dupixent would be the only biologic therapy for COPD and the first new treatment approach for this disease in more than a decade Regulatory submissions are also under review in China and Europe Dupixent is the leading biologic treatment for all five of its FDA-approved indications in new-to-brand prescriptions in the U.S. TARRYTOWN, N.Y. and PARIS, Feb. 23, 2024 (GLOBE NEWSWIRE) Regeneron Pharmaceuticals, ....

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