This study is a post-marketing surveillance of lenvatinib in participants with unresectable thyroid cancer. The objectives of this study are to capture unknown adverse reactions, incidences of adverse drug reaction, efficacy, factors considered to have effect to safety and effectiveness, and incidences of hypertension, hemorrhagic events and thromboembolic event, and liver disorder.
Study Type
OBSERVATIONAL
Enrollment
629
24mg once daily oral dosing to Unresectable thyroid cancer patients
Unnamed facility
Osaka, Japan
Unnamed facility
Tokyo, Japan
Number of participants with adverse events (AEs)/adverse drug reactions (ADRs)
Time frame: up to 1 year
Overall survival (OS)
Time frame: up to 1 year
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