Study identifier:D4200C00088
ClinicalTrials.gov identifier:NCT01298323
EudraCT identifier:2010-023428-26
CTIS identifier:N/A
A Randomized,Int.,Open-Label Phase III Study to Assess the Effect of a Patient Outreach Program on the Percentage of Time Patients with Locally Advanced or Metastatic MTC Experience Grade 2 or Higher AEs in the First 12 Months of Treatment with Vandetanib
Locally Advanced or Metastatic Medullary Thyroid Cancer
Phase 3
No
Vandetanib
All
217
Interventional
18 Years - 130 Years
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Mar 2016 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Active Comparator: Vandetanib Control Control - treatment 300mg vandetanib opel label | Drug: Vandetanib Treatment 300mg vandetanib opel label. |
Experimental: Experimental Experimental - treatment 300mg vandetanib opel label | Behavioral: Patient outreach Patients will be contacted at week 1 and then every 2 weeks until completion of 52 weeks to detect/treat AEs sooner Drug: Vandetanib Treatment 300mg vandetanib opel label. |