Vandetanib (ZD6474)
Drugonce daily oral dose
Other names: ZACTIMA™
NCT Number: NCT00494481
To assess the efficacy of ZD6474 in combination with docetaxel in the treatment of ABC using the progression event count methodology
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Notify Me18 year and older
Female
Interventional
Phase 2
Research Site, Budapest, Hungary
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
once daily oral dose
Other names: ZACTIMA™
intravenous infusion
Other names: Taxotere®
Time frame: RECIST tumour assessments carried out at screening (within 3 weeks before the 1st dose) and then as per site clinical practice until objective progression. The only additional mandatory RECIST assessment is at the point of data cut-off
Number of patients with objective disease progression or death (by any cause in the absence of objective progression)
Genzyme, a Sanofi Company
Industry
A Phase II, Double-blind, Placebo Controlled, Randomized Study to Assess the Efficacy and Safety of ZD6474 in Combination With Docetaxel (Taxotere™) vs Docetaxel Alone as 2nd Line Treatment for Advanced Breast Cancer (ABC).
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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