PRESS RELEASE published on 09/27/2024 at 15:35, 1 year 4 months ago Press Release: Dupixent approved in the US as the first-ever biologic medicine for patients with COPD US FDA approves Dupixent as the first-ever biologic medicine for COPD, based on phase 3 studies showing significant reduction in exacerbations and improved lung function. Dupixent is now leading in new-to-brand prescriptions for FDA-approved indications FDA Approval Dupixent COPD Treatment Biologic Medicine Phase 3 Studies
BRIEF published on 09/27/2024 at 13:05, 1 year 4 months ago Dupixent Authorized in China as First Biologic Medicine for COPD Patients China Approval COPD Dupixent Biologic Medicine
PRESS RELEASE published on 09/27/2024 at 13:00, 1 year 4 months ago Press Release: Dupixent approved in China as the first-ever biologic medicine for patients with COPD Dupixent approved in China as the first-ever biologic medicine for COPD patients, following landmark phase 3 studies. Approval crucial for addressing COPD burden in China China COPD Dupixent Biologic Medicine Phase 3 Studies
BRIEF published on 09/21/2024 at 00:41, 1 year 4 months ago Sarclisa Approved in the United States for the Treatment of Multiple Myeloma FDA Sanofi Multiple Myeloma Sarclisa First Line Treatment
BRIEF published on 09/20/2024 at 13:50, 1 year 4 months ago CHMP recommends approval of Dupixent for children aged 12 months and older Children Medicine Dupixent CHMP Esophagitis
PRESS RELEASE published on 09/20/2024 at 13:45, 1 year 4 months ago Press Release: Dupixent recommended for EU approval by the CHMP to treat eosinophilic esophagitis in children as young as 1 year old Dupixent recommended for EU approval by the CHMP to treat eosinophilic esophagitis in children as young as 1 year old based on positive phase 3 study results. Dupixent would be the first medicine indicated for EoE in this age group Children Dupixent CHMP EU Approval Eosinophilic Esophagitis
BRIEF published on 09/20/2024 at 11:35, 1 year 4 months ago Sanofi's Tolebrutinib Shows Promise in Delaying Disability Progression in MS Multiple Sclerosis ECTRIMS 2024 Tolebrutinib HERCULES Study Disability Progression
PRESS RELEASE published on 09/20/2024 at 11:30, 1 year 4 months ago Press Release: Tolebrutinib demonstrated a 31% delay in time to onset of confirmed disability progression in non-relapsing secondary progressive multiple sclerosis phase 3 study Study shows tolebrutinib delays disability progression in non-relapsing secondary progressive MS by 31%; global regulatory submissions in H2 2024. ECTRIMS 2024 data presented ECTRIMS 2024 Tolebrutinib Disability Progression Secondary Progressive MS Global Regulatory Submissions
BRIEF published on 09/16/2024 at 18:49, 1 year 4 months ago Sanofi Reports Share and Voting Rights Data for August 2024 Voting Rights Shares Investor Relations Sanofi August 2024
PRESS RELEASE published on 09/16/2024 at 18:44, 1 year 4 months ago Sanofi: Information concerning the total number of voting rights and shares - August 2024 Sanofi discloses total number of voting rights and shares as per French Commercial Code and AMF regulations Voting Rights French Commercial Code Shares AMF Regulations Sanofi
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