Cantor Fitzgerald thinks U.S approval around the August 20 FDA action date for vorasidenib is “nearly assured” for given the drug has breakthrough designation in glioma, a tumor type of high unmet need, and led to a more than doubling of progression free survival in a Phase 3 trial. Investors had been underestimating the value of vorasidenib royalties to Agios Pharmaceuticals, the analyst tells investors in a research note after the company sold its 15% U.S. royalty interest in Servier’s vorasidenib to Royalty Pharma for $905M. . Agios will keep the $200M approval milestone, and will be entitled to a 3% royalty on annual U.S. sales above $1B, the firm notes. With Agios shares at a market cap of just below $1.8B, Cantor believes investors are paying nothing for Pyrukynd. Cantor believes Pyrukynd “could easily” become a $1B product and it recommends investors “take advantage of this market inefficiency.” It keeps an Overweight rating on the shares.
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