Skip to content
Study details
Enrolling now

A Study of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations

Turning Point Therapeutics, Inc.
NCT IDNCT04094610ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

75

Study length

about 7.6 years

Ages

≤25

Locations

20 sites in CA, CO, FL +12

About this study

This trial is testing a treatment called repotrectinib to see if it's safe and effective for children and young adults with certain types of cancer. The goal is to find the best dose level and determine if this drug can help fight the cancer.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Oral repotrectinib (TPX-0005)
PhasePhase 1/Phase 2
DrugOral repotrectinib (TPX-0005)
Routeoral
Primary goalOverall Response Rate (ORR) (Phase 2)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

repotrectinib

Drug routes

oral (Oral Capsule)

Endpoints

Primary: Overall Response Rate (ORR) (Phase 2)

Secondary: Area under the concentration versus time curve of repotrectinib in plasma (AUC), Central Nervous System Progression-Free Survival (CNS-PFS) (Phase 2), Duration of response (DOR) (Phase 1 and Phase 2), Intracranial objective response rate (IC-ORR) (Phase 1 and Phase 2), Maximum concentration of repotrectinib in plasma (Cmax), Overall Response Rate (ORR) (Phase 1), Overall survival (OS) (Phase 2), Progression-free survival (PFS) (Phase 2)

Body systems

Oncology