Source: Medthority

Nuvation Bio: FDA accepts NDA for taletrectinib, sets PDUFA date

The FDA has accepted Nuvation Bio's NDA for taletrectinib to treat advanced ROS1-positive NSCLC, with a PDUFA date set for June 23, 2025

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Annual Revenue
$5.0-25M
Employees
100-250
David Hung's photo - President & CEO of Nuvation Bio

President & CEO

David Hung

CEO Approval Rating

84/100

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