PRESS RELEASE published on 09/27/2024 at 15:35, 1 year 8 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
PRESS RELEASE published on 09/27/2024 at 15:35, 1 year 8 months ago Communiqué de presse : Dupixent est le premier médicament biologique approuvé aux États-Unis pour le traitement de la BPCO La FDA approuve Dupixent comme premier médicament biologique pour la BPCO aux États-Unis, offrant un nouveau traitement aux patients inadéquatement contrôlés. Résultats positifs des études BOREAS et NOTUS FDA Traitement Études BPCO Dupixent
BRIEF published on 09/27/2024 at 13:05, 1 year 8 months ago Dupixent Authorized in China as First Biologic Medicine for COPD Patients China Approval COPD Dupixent Biologic Medicine
BRIEF published on 09/27/2024 at 13:05, 1 year 8 months ago Dupixent autorisé en Chine comme premier médicament biologique pour les patients atteints de BPCO Chine MPoC Approbation Dupixent Médecine Biologique
PRESS RELEASE published on 09/27/2024 at 13:00, 1 year 8 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
PRESS RELEASE published on 09/27/2024 at 13:00, 1 year 8 months ago Communiqué de presse : Dupixent, premier médicament biologique approuvé en Chine pour le traitement de la BPCO Dupixent, premier médicament biologique approuvé en Chine pour le traitement de la BPCO, réduit les exacerbations et améliore la fonction respiratoire. Approbation suite à études de phase III Traitement Chine Approbation BPCO Dupixent
BRIEF published on 09/21/2024 at 00:41, 1 year 9 months ago Approbation du Sarclisa aux États-Unis pour le traitement du myélome multiple FDA Sanofi Myélome Multiple Sarclisa Traitement De Première Ligne
BRIEF published on 09/21/2024 at 00:41, 1 year 9 months ago Sarclisa Approved in the United States for the Treatment of Multiple Myeloma FDA Sanofi Multiple Myeloma Sarclisa First Line Treatment
PRESS RELEASE published on 09/21/2024 at 00:36, 1 year 9 months ago Communiqué de presse : Approbation du Sarclisa aux États-Unis : premier anti-CD38, en association avec un traitement conventionnel, pour les patients atteints d’un myélome multiple nouvellement diagnostiqué (...) La FDA approuve le Sarclisa aux États-Unis en association avec un traitement conventionnel pour les patients atteints de myélome multiple nouvellement diagnostiqué, non éligibles à une transplantation. Sanofi comble un vide thérapeutique important FDA Traitement Sanofi Myélome Multiple Sarclisa
BRIEF published on 09/20/2024 at 13:50, 1 year 9 months ago Le CHMP recommande l'approbation du Dupixent pour les enfants de 12 mois et plus Médicament Dupixent Enfants CHMP Œsophagite
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