‘Breakthrough’ Fee Eyed As Deterrent To Frivolous Requests

Companies currently face little risk in seeking the designation because there is no financial cost and FDA denial is confidential.

A “breakthrough therapy” user fee might help deter product sponsors from submitting frivolous designation requests with impunity, a cancer expert suggested at the Brookings meeting on the expedited regulatory program April 24.

George Demetri, a professor of medicine at Harvard and senior VP for experimental therapeutics at the Dana-Farber Cancer Institute, said that companies with questionable data might be less inclined to...

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