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Terminated

An Efficacy and Safety Study With Vandetanib to Treat Inoperable or Relapsed Malignant Mesothelioma

By April 24, 2017No Comments

Condition

Mesothelioma

Estimated Enrollment: 25

Age Group: 18 Years and older   (Adult, Senior)

Gender: All

Study Type: Interventional

Study Design Allocation: Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Open Label|Primary Purpose: Treatment

Study ID Numbers: D4200C00075|EUDRACT Number 2007-003633-16

Study First Received: January 9, 2008

Last Updated: August 29, 2016

Estimated Primary Completion Date: January 2010

 

Primary Outcome Measures:

Number of Participants With Disease Control.|Number of Participants With Objective Response.|Progression-free Survival (PFS)|Overall Survival (OS)

Sponsors and Collaborators:

Genzyme, a Sanofi Company|Sanofi

Website Link: https://ClinicalTrials.gov/show/NCT00597116

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