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In this registry it is planned to include all Belgian patients diagnosed with aggressive and symptomatic unresectable locally advanced or metastatic Medullary Thyroid Cancer (MTC) who have been prescribed Caprelsa® (vandetanib).
The characteristics of patients receiving Caprelsa® (vandetanib) will be described. Therefore real life data regarding demographic characteristics, evolution of the disease, RET mutation status, the treatment before, during and after vandetanib, dose and duration of treatment with Caprelsa® (vandetanib) and time of progression or death (if applicable) will be included.
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Inclusion and exclusion criteria
Inclusion criteria
The subject population that will be observed in this registry, must fulfil all of the following criteria:
The prescription of the medicinal product is clearly separated from the decision to include the subject in the registry.
Exclusion criteria Not applicable since patients participating in another study can take part in this registry.
10 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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