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.
Study Type
OBSERVATIONAL
Enrollment
10
As per product label
Bristol Myers Squibb Pharmaceutical Korea Ltd
Seoul, South Korea
Number of participants experiencing adverse events
Adverse events include: adverse drug reaction (ADR), serious adverse event (SAE), serious adverse drug reaction (SADR), unexpected adverse event (AE), unexpected ADR, unexpected SAE or SADR and adverse events of special interest (AESI)
Time frame: Up to 12 months
Number of participants achieving objective tumor response according to RECIST version 1.1
Time frame: Up to 12 months
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