Synonyms: Augtyro® | example 93 [US20170334929A1] | TPX-0005 | TPX0005
repotrectinib is an approved drug (FDA (2023))
Compound class:
Synthetic organic
Comment: Repotrectinib (TPX-0005) is a next-generation oral ROS1/NTRK/ALK inhibitor that was rationally designed to overcome tumour resistance due to acquired mutations in these kinases [3-4]. The chemical structure is claimed as example 93 in TP Therapeutics' patent US20170334929A1 [1].
Ligand Activity Visualisation ChartsThese are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts. ✖ |
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No information available. |
Summary of Clinical Use |
Repotrectinib (TPX-0005) was advanced to a first-in-human dose-escalation Phase 1/2 clinical evaluation in ALK-, ROS1-, or NTRK1-3-rearranged solid and hematological malignancies. Click here to link to ClinicalTrials.gov's full list of TPX-0005 trials. The FDA granted Breakthrough Therapy Designation for repotrectinib in October 2021, as a treatment for NTRK gene fusion +ve advanced solid tumours that have progressed following prior treatment with ≥1 tyrosine kinase inhibitor therapies, and for which there is no other suitable treatment. FDA approval was granted in November 2023 [2], to treat locally advanced or metastatic ROS1-positive non-small cell lung cancer. FDA approval was expanded in June 2024 to include treatment of any patients ≥12 years old with locally advanced/metastatic or unresectable NTRK gene fusion +ve solid tumours, and for which there is no satisfactory alternative therapy. |
Clinical Trials | |||||
Clinical Trial ID | Title | Type | Source | Comment | References |
NCT03093116 | A Study of Repotrectinib (TPX-0005) in Patients With Advanced Solid Tumors Harboring ALK, ROS1, or NTRK1-3 Rearrangements | Phase 1/Phase 2 Interventional | Turning Point Therapeutics, Inc. | ||
NCT04094610 | A Study of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations | Phase 1/Phase 2 Interventional | Turning Point Therapeutics, Inc. |