Press Release: Dupixent approved in the US as the first-ever biologic medicine for patients with COPD [Yahoo! Finance]
Sanofi - American Depositary Shares (SNY)
US:NYSE Investor Relations:
sanofi.com/en/investors
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Source: Yahoo! Finance
Dupixent is indicated for the approximately 300,000 adults in the US with inadequately controlled COPD and an eosinophilic phenotype Following recent approvals in the EU and China, the US approval is based on two landmark phase 3 studies that showed Dupixent achieved significant reduction in exacerbations, and also showed improvements in lung function and health-related quality of life compared to placebo Dupixent is the leading biologic medicine for all of its FDA-approved indications in new-to-brand prescriptions, and the most prescribed biologic by pulmonologists in the US Paris and Tarrytown, NY, September 27, 2024. The US Food and Drug Administration (FDA) has approved Dupixent (dupilumab) as an add-on maintenance treatment of adults with inadequately controlled chronic obstructive pulmonary disease (COPD) and an eosinophilic phenotype. Dupixent is the first biologic medicine approved in the US to treat these patients. Jean Wright, M.D. Chief Executive Officer at The C
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News
- FDA greenlights Regeneron's Dupixent for the treatment of COPD [Yahoo! Finance]Yahoo! Finance
- Regeneron/ Sanofi granted FDA label expansion for Dupixent in COPD Sep. 27, 2024 1:16 PM ET By: Dulan Lokuwithana , SA News Editor [Seeking Alpha]Seeking Alpha
- Sanofi/Regeneron's Dupixent set to dominate COPD biologics market following FDA approval [Yahoo! Finance]Yahoo! Finance
- Press Release: Dupixent approved in the US as the first-ever biologic medicine for patients with COPDGlobeNewswire
- Press Release: Dupixent approved in China as the first-ever biologic medicine for patients with COPDGlobeNewswire
SNY
Sec Filings
- 9/24/24 - Form 6-K
- 9/13/24 - Form 6-K
- 9/3/24 - Form 6-K
- SNY's page on the SEC website