Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 5:03 PM
Ignite Modification Date: 2025-12-24 @ 5:03 PM
NCT ID: NCT02109250
Eligibility Criteria: Inclusion criteria The subject population that will be observed in this registry, must fulfil all of the following criteria: 1. Provision of subject Informed Consent 2. Patients diagnosed with aggressive and symptomatic unresectable locally advanced or metastatic MTC 3. Patients who already received a prescription for vandetanib in accordance with the scientific leaflet and fulfilling the reimbursement criteria of vandetanib and who are currently treated or have been treated with vandetanib 100 mg or 300 mg tablets. 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.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT02109250
Study Brief:
Protocol Section: NCT02109250