One of the drug industry’s best-selling therapies could be closer than expected to becoming the first biologic to treat COPD, or chronic obstructive pulmonary disease.
In announcing third-quarter results on Thursday, Regeneron said an interim analysis of a Phase III COPD study could support filing Dupixent for approval with the FDA. The New York biotech said the data monitoring committee plans to take a look at the interim data later this year and recent feedback from the FDA supported this plan.
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