Myovant shows disappointing prostate cancer data on the way to the FDA, stock sinks
Myovant $MYOV has been prepping relugolix for advanced prostate cancer over the last several months, looking to improve upon the old standard in AbbVie’s Lupron. But new data out Tuesday will not help its cause.
Relugolix failed to meet a critical secondary endpoint in a Phase III trial and did not achieve statistical superiority for castration resistance-free survival after 48 weeks compared to the AbbVie drug. In the subgroup of men with metastatic prostate cancer, 74% of those treated with relugolix were alive and castration-resistance free through 48 weeks compared to 75% on Lupron. The p-value of the study was 0.84.
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