US FDA's Woodcock: Sponsors Have To Make Right-To-Try Decisions

FDA must still determine internal procedures for receiving annual reports and handling adverse events through the controversial pathway that encourages access to unapproved therapies.

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BOSTON – Usually the US FDA encourages sponsors to seek its advice. But when it comes to tips on the Right To Try process, the agency appears intent on remaining silent.

Instead, FDA is placing the burden for deciding eligibility for the alternative expanded access pathway entirely on sponsors.

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