FDA hold PTG-300: Protagonist Therapeutics Reports... - MPN Voice

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FDA hold PTG-300

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Protagonist Therapeutics Reports FDA Clinical Hold on Rusfertide (PTG-300) Clinical Development Program due to tumorigenicity.

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Manouche

« Belviq had similar rat tumor issues but allowed to complete trial & ultimately FDA approval - & this was for obesity

Highly unlikely for a deadly disease like polycythemia with no approved therapy will not have clinical hold removed on Rusfertide »

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