The FDA has accepted Sanofi and Regeneron’s application to expand Dupixent’s use, with a decision expected by April 2025.

Regeneron and Sanofi's Dupixent sBLA for treating chronic spontaneous urticaria in patients 12+ gets FDA review, with a ...

Regeneron (REGN) and Sanofi (SNY) announced that the FDA has accepted for review the resubmission of the supplemental Biologics License ...

French drug major Sanofi (SNY) and Regeneron Pharmaceuticals, Inc. (REGN) announced Friday that the U.S. Food and Drug Administration ...

The FDA has provided a date of April 18, 2025, to review the application for Dupixent to treat patients with chronic ...

The FDA last year turned away the companies' application and asked for additional efficacy data. Regeneron and Sanofi said the resubmission adds results from an additional Phase 3 study of Dupixent in ...

This expansion positions Dupixent as the first targeted therapy for COPD ... Further boosting the pipeline, mid-stage drugs ...

A major news story from Sanofi this month is that "The European Medicines Agency has approved Dupixent (dupilumab) to treat ...

你是否曾经听说过嗜酸性食管炎（EoE）？这种慢性炎症性疾病在儿童中尤为常见，它会导致食管受损和功能障碍。想象一下，一个孩子因为吞咽困难、胃酸反流和腹部不适而无法正常进食，这对他们的成长和发育会带来多大的影响！近日，再生元（Regeneron Pharmaceuticals）与赛诺菲（Sanofi）联合宣布，其重磅疗法Dupixent（dupilumab）已获欧盟批准用于治疗1至11岁的EoE儿童患 ...

Resubmission includes new pivotal data which confirm Dupixent significantly reduced itch and hive activity More than 300,000 people in the U.S. suffer from CSU that is inadequately controlled by ...

The safety results from the EoE KIDS study were consistent with the known safety profile of Dupixent in adolescents and ...

Paris: Sanofi has announced that the European Medicines Agency has approved Dupixent (dupilumab) to treat eosinophilic ...