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NCT07599007Not yet recruiting

Repotrectinib Post-Marketing Surveillance in Korean Patients With ROS1-Positive Non-Small Cell Lung Cancer (NSCLC) or Solid Tumors Harboring a Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion

AUGTYRO™ (Repotrectinib) Post-Marketing Surveillance in Korean Patients With Locally Advanced or Metastatic Ros1-Positive NSCLC or Solid Tumors Harboring a NTRK Gene Fusion

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

This observational study evaluates the real-world safety and effectiveness of repotrectinib in Korean participants with locally advanced or metastatic ROS1-positive non-small cell lung cancer or solid tumors harboring neurotrophic tyrosine receptor kinase (NTRK) gene fusions. Participants receiving repotrectinib in routine clinical practice will be followed for up to 12 months or until the end of the 2-year surveillance period, whichever occurs first.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
10 (estimated)
First submitted
14 May 2026
Start date
31 Oct 2026
Primary completion date
30 Dec 2027
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT07599007

What you commit to

  • Study type: Observational
  • Planned participants: 10
  • From 31 Oct 2026 to the primary completion date, 30 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with repotrectinib for indications not approved in Korea
  • Treatment with repotrectinib at dosages not approved in Korea

Other

  • Contraindication to repotrectinib according to MFDS prescribing information

Who the study is looking for

  • Participants aged ≥19 years with histologically OR cytologically confirmed locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC)
  • Participants aged ≥12 years with solid tumors harboring Neurotrophic Tyrosine Receptor Kinase (NTRK) gene fusions
  • Documented ROS1 or NTRK 1-3 gene fusion by validated local testing
  • Written informed consent

Age in the registry: 12 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bristol Myers Squibb Pharmaceutical Korea Ltd
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.