PRESS RELEASE published on 12/24/2025 at 07:15, 7 months 19 days ago Communiqué de presse : Sanofi va acquérir Dynavax et ajouter un vaccin commercialisé contre l’hépatite B pour adultes et un candidat vaccin de phase 1/2 contre le zona au pipeline Sanofi acquiert Dynavax pour renforcer sa présence dans la vaccination des adultes avec un vaccin contre l'hépatite B et un candidat vaccin contre le zona. La transaction est estimée à environ 2,2 milliards de dollars. Accord approuvé par le Conseil d'administration de Dynavax Acquisition Sanofi Vaccin Hépatite B Zona
PRESS RELEASE published on 12/24/2025 at 07:15, 7 months 19 days ago Press Release: Sanofi to acquire Dynavax, adding a marketed adult hepatitis B vaccine and phase 1/2 shingles candidate to the pipeline Sanofi announces acquisition of Dynavax Technologies Corporation, expanding adult vaccine portfolio with hepatitis B and shingles candidates. Merger valued at $2.2 billion Acquisition Sanofi Vaccines Dynavax Hepatitis B
BRIEF published on 12/24/2025 at 07:05, 7 months 19 days ago Sanofi Faces Delay in FDA Approval for Tolebrutinib in MS Treatment FDA Sanofi Tolebrutinib MS Treatment Regulatory Delay
BRIEF published on 12/24/2025 at 07:05, 7 months 19 days ago Sanofi fait face à un retard dans l'approbation par la FDA du tolebrutinib pour le traitement de la SEP. FDA Sanofi Tolebrutinib Retard Réglementaire Traitement De La SEP
PRESS RELEASE published on 12/24/2025 at 07:00, 7 months 19 days ago Press Release: Sanofi provides update on tolebrutinib regulatory submission in non-relapsing secondary progressive multiple sclerosis Sanofi provides update on tolebrutinib regulatory submission for non-relapsing secondary progressive multiple sclerosis, with FDA issuing a complete response letter and further guidance expected in Q1 2026 FDA Multiple Sclerosis Sanofi Tolebrutinib Regulatory Submission
PRESS RELEASE published on 12/24/2025 at 07:00, 7 months 19 days ago Communiqué de presse : Sanofi fait le point sur la soumission réglementaire du tolebrutinib dans la sclérose en plaques secondaire progressive non-récurrente Sanofi fait le point sur la soumission réglementaire du tolebrutinib dans la sclérose en plaques secondaire progressive non-récurrente. La FDA émet une lettre de réponse complète pour le tolebrutinib contre la SEPSPnr FDA Sclérose En Plaques Sanofi Tolebrutinib SEPSPnr
BRIEF published on 12/23/2025 at 15:11, 7 months 20 days ago Sanofi's Wayrilz Gets EU Approval for Treating Immune Thrombocytopenia Sanofi EU Approval BTK Inhibitor Wayrilz Immune Thrombocytopenia
BRIEF published on 12/23/2025 at 15:11, 7 months 20 days ago Sanofi's Wayrilz receives EU approval for the treatment of IPT EU Sanofi TPI Wayrilz BTK
BRIEF published on 12/23/2025 at 15:11, 7 months 20 days ago Le Wayrilz de Sanofi obtient l'approbation de l'UE pour le traitement de la thrombocytopénie immunitaire Sanofi Wayrilz Inhibiteur De BTK Thrombocytopénie Immunitaire Approbation De L'UE
BRIEF published on 12/23/2025 at 15:11, 7 months 20 days ago Wayrilz de Sanofi reçoit l'approbation de l'UE pour le traitement de la TPI EU Sanofi TPI Wayrilz BTK
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