Registry for Molecular Testing, Treatment and Outcome of Patients With Solid Tumors Harboring a N… (NCT04557813) | Clinical Trial Compass
CompletedNot Applicable
Registry for Molecular Testing, Treatment and Outcome of Patients With Solid Tumors Harboring a NTRK Gene Fusion
Germany88 participantsStarted 2020-12-02
Plain-language summary
The objective of this registry is to analyze treatment reality and outcome of patients with locally advanced or metastatic solid tumors harboring a fusion of NTRK1, NTRK2 or NTRK3
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Locally advanced or metastatic solid tumor with a documented NTRK gene fusion, based on a validated assay (according to current ESMO recommendations), or the provision of tumor material for central retesting
* Molecular pathology or molecular diagnostics report with details on NTRK gene fusion testing must be available
* Aged ≥ 18 years
* Signed and dated informed consent form (ICF) (only if patient is alive at time of data entry into the project; not applicable for inclusion of deceased patients' data)
Exclusion Criteria:
* Treatment with a TRK inhibitor prior to Sept 19th, 2019 (Germany) or May 28th, 2020 (Switzerland)
* Participation in a clinical trial with a TRK inhibitor before or at enrolment (liv-ing patients) or before inclusion (deceased patients)
* Deceased patients who have explicitly contradicted further use of data
What they're measuring
1
Overall response rate
Timeframe: through study completion, at least 1 year