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Tuesday, March 26, 2019

Aimmune data sets stage for EU submission in mid-2019, says JMP

JMP Securities analyst Liisa Bayko said Aimmune’s “strong” efficacy and safety data from the Phase 3 ARTEMIS study sets the stage for a marketing authorization application to the European Medicines Agency in mid-2019. The analyst, who assigns a 90% probability of success for AR101 in peanut allergy, keeps an Outperform rating and $40 price target on Aimmune shares.

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