Patients who are morbidly obese or who have other high-risk diseases may get more attention from pharma companies in years to come if the US Food and Drug Administration takes the recommendation of The President’s science advisors, who unveiled a plan to double the number of prescription drug approvals for certain diseases on Tuesday (September 25).
The advisory panel proposed that the FDA approve certain drugs with side effects that may otherwise prevent approval, for use in patients who have no other options for treatment, but restrict those drugs from being used in the general population. For example, an individual with morbid obesity may be willing to take a drug with more severe side effects than a patient with moderate obesity if that drug is effective at reducing the obesity. However, those with milder obesity could not be prescribed the drug.
The move could "help deliver promising new medications to ...
