Turning Point Therapeutics granted fast-track designation for repotrectinib in NTRK positive TKI pre-treated advanced solid tumours

Turning Point Therapeutics

24 August 2020 - Turning Point Therapeutics today announced the FDA granted a third fast-track designation to its lead drug candidate repotrectinib.

The designation was granted for the treatment of patients with advanced solid tumours that have an NTRK gene fusion who have progressed following treatment with at least one prior line of chemotherapy and one or two prior TRK tyrosine kinase inhibitors (TKIs) and have no satisfactory alternative treatments. 

Repotrectinib was previously granted two fast track designations for the treatment of ROS1 positive advanced non-small cell lung cancer patients, first for patients with one prior line of platinum-based chemotherapy and one prior ROS1 TKI, and second for patients without prior ROS1 TKI treatment.

Read Turning Point Therapeutics press release

Michael Wonder

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Michael Wonder

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Cancer , Medicine , US , Fast track