FDA approval for lung cancer drug Gavreto

7 September 2020

The US Food and Drug Administration (FDA) has approved Gavreto (pralsetinib) for the treatment of adult patients with metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer (NSCLC) as detected by an FDA approved test, US precision cancer therapy specialist Blueprint Medicines (Nasdaq: BPMC) announced on Friday, when the firm’s shares moved up 2.9% to $75.00 in after-hours trading.

The approval is based on data from the Phase I/II ARROW clinical trial, which showed efficacy for Gavreto in patients with RET fusion-positive NSCLC with or without prior therapy, and regardless of RET fusion partner or central nervous system involvement.

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