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Sanofi: ASCO: Sarclisa is first anti-CD38 to significantly improve progression-free survival in combination with VRd for newly diagnosed transplant-ineligible multiple myeloma in phase 3

ASCO: Sarclisa is first anti-CD38 to significantly improve progression-free survival in combination with VRd for newly diagnosed transplant-ineligible multiple myeloma in phase 3 Sarclisa, in combination ....

France General , United States , Tarik Elgoutni , Thomas Kudsk Larsen , Felix Lauscher , Keita Browne , Evan Berland , Peterc Adamson , Sandrine Guendoul , Timothy Gilbert , Thierry Facon , Nathalie Pham , French Academy Of Medicine , Drug Administration , American Society Of Clinical Oncology , Lille University Hospital , Global Development Head , European Hematology Association , World Health Organization , Congress On , European Union , Department Of Haematology , American Society , Clinical Oncology , New England Journal , French Academy ,

Press Release: ASCO: Sarclisa is first anti-CD38 to significantly improve progression-free survival in combination with VRd for newly diagnosed transplant-ineligible multiple myeloma in phase 3

Press Release: ASCO: Sarclisa is first anti-CD38 to significantly improve progression-free survival in combination with VRd for newly diagnosed transplant-ineligible multiple myeloma in phase 3
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France General , United States , Evan Berland , Tarik Elgoutni , Peterc Adamson , Sandrine Guendoul , Timothy Gilbert , Thomas Kudsk Larsen , Nathalie Pham , Felix Lauscher , Thierry Facon , Keita Browne , European Union , World Health Organization , Lille University Hospital , Drug Administration , Congress On , French Academy Of Medicine , American Society Of Clinical Oncology , Global Development Head , European Hematology Association , Department Of Haematology , American Society , Clinical Oncology , New England Journal , French Academy ,

Press Release: Update on FDA priority review of Dupixent for the treatment of COPD patients with type 2 inflammation

Press Release: Update on FDA priority review of Dupixent for the treatment of COPD patients with type 2 inflammation
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France General , United States , Timothy Gilbert , Sandrine Guendoul , Thomas Kudsk Larsen , Hannah Kwagh , Evan Berland , Nathalie Pham , Vesna Tosic , Tarik Elgoutni , Felix Lauscher , Corentine Driancourt , Dupilumab Development Program , Drug Administration , European Medicines Agency , Committee For Medicinal Products Human Use , Regeneron Pharmaceuticals Inc , Us Department Of Justice , Clinical Research Program , European Union , Exchange Commission , Regeneron Genetics Center , Biologics License Application , Medicinal Products , Human Use , Regeneron Genetics ,

Dupixent® (dupilumab) Recommended for EU Approval by the CHMP to Treat Patients with COPD

Recommendation for adults with uncontrolled COPD with raised blood eosinophils based on data from two landmark Phase 3 trials demonstrating Dupixent significantly reduced exacerbations and improved. ....

France General , United States , Georged Yancopoulos , Hannah Kwagh , Timothy Gilbert , Regeneron Velocimmune , Nathalie Pham , Sandrine Guendoul , Evan Berland , Felix Lauscher , Arnaud Delepine , Thomas Kudsk Larsen , Tarik Elgoutni , Corentine Driancourt , Vesna Tosic , Clinical Research Program , Us Department Of Justice , European Commission , Exchange Commission , European Union , Dupilumab Development Program , European Commission Of Dupixent , Regeneron Genetics Center , Globenewswire Inc , Drug Administration , Regeneron Pharmaceuticals Inc ,

Press Release: Dupixent recommended for EU approval by the CHMP to treat patients with COPD

Dupixent recommended for EU approval by the CHMP to treat patients with COPD Recommendation for adults with uncontrolled COPD with raised blood eosinophils based on data from two landmark Phase 3. ....

France General , United States , Evan Berland , Nathalie Pham , Sandrine Guendoul , Tarik Elgoutni , Thomas Kudsk Larsen , Corentine Driancourt , Vesna Tosic , Hannah Kwagh , Timothy Gilbert , Felix Lauscher , European Commission Of Dupixent , Drug Administration , Regeneron Pharmaceuticals Inc , Regeneron Genetics Center , Us Department Of Justice , Clinical Research Program , European Union , Exchange Commission , Dupilumab Development Program , European Commission , European Medicines Agency , Medicinal Products , Human Use , Respiratory Questionnaire ,