Viewing Study NCT02109250


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Study NCT ID: NCT02109250
Status: COMPLETED
Last Update Posted: 2017-05-02
First Post: 2014-03-27
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: CAPRELSA® REGISTRY: a Belgian Registry to Evaluate the Use of Vandetanib (Caprelsa®) in Current Clinical Practice
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Study Design

Study Type: OBSERVATIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: True
Target Duration: 16 Months
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Bio Spec Retention: None
Bio Spec Description: None
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