FDA approves Allergan’s eye pressure drug
The Lumigan first-line indication is in addition to the product’s already established use as a second-line treatment, for which the FDA approved the drug in 2001. Since its
The European Commission (EC) has granted orphan designation to Lundbeck’s investigational monoclonal antibody asedebart (Lu AG13909) for the treatment of Cushing’s syndrome of endogenous origin.