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Trial Summary

Phase 1 dose escalation will determine the first cycle dose-limiting toxicities (DLTs), themaximum tolerated dose (MTD), the biologically effective dose and recommended Phase 2 dose(RP2D) of repotrectinib given to adult subjects with advanced solid malignant tumors.



ACTRN/NCT /ethics:


Scientific title:

A Study of Repotrectinib (TPX-0005) in Patients With Advanced Solid Tumors Harboring ALK, ROS1, or NTRK1-3 Rearrangements

Sponsor / Cooperative group:

Turning Point Therapeutics

Trial & Patient Characteristics

Cancer TypeAll cancers
Trial TypeTreatment
PhasePhase I; Phase II
Age Range18 years and older
Tumour Stream -
Cancer StageLocally Recurrent or Locally Advanced; Metastatic or Widespread
Anticipated Start Date2017-02-27
Anticipated End Date2022-12-31

Participating Hospitals

HospitalFlinders Medical Centre
Clinical Trial CoordinatorAlison Richards
Phone08 8206 4835
Principal InvestigatorProfessor Chris Karapetis
Recruitment StatusRecruiting