On Wednesday, Sanofi (NASDAQ: SNY) and partner Regeneron (NASDAQ: REGN) won European Union approval for wider use of their Dupixent injection in patients with chronic lung disease, a rare case of the EU clearing a drug faster than the United States.
The EU Commission approved Dupixent to treat chronic obstructive pulmonary disease (COPD) in patients that cannot be helped by standard inhaled drugs, Sanofi said in a statement, following a recommendation by the European Medicines Agency (EMA) at the end of May.
The debilitating disease is also known as ‘smoker’s lungs’ because in Western countries it primarily affects cigarette smokers.
For its part, the U.S. Food and Drug Administration (FDA) in May pushed back the deadline for reviewing Dupixent in COPD by three months to Sept. 27 as it demanded additional efficacy data.
The potentially deadly disease, which causes restricted airflow and breathing problems, affects nearly 16 million U.S. adults and over 35 million people in Europe, according to government data.
French drugmaker Sanofi said in April it expects the target patient population eligible for the drug to be roughly 300,000 in the U.S. alone.
In Europe, the final decision rests with the European Commission, which usually follows EMA’s guidance.
The drug is already approved in many countries for various immune system-related conditions like asthma and eczema.
Sanofi reported 10.7 billion euros in 2023 Dupixent revenues, which includes Regeneron’s share, and has forecast about 13 billion euros for this year.
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(Source: ReutersReuters)
