Sanofi-Aventis Administrative Office
Barcelona, Spain
NCT Number: NCT00421824
Primary:
* To assess complete pathological response rate of both strategies.
Secondary:
* Safety profile * To assess downstaging rate of both strategies. * To compare relative dose intensity of oxaliplatin and capecitabine of both strategies * To compare time to progression and overall survival of both strategies.
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Notify Me18 year–75 year
All sexes
Interventional
Phase 2
Barcelona, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
OXA 130 D1 + Capecitabine 2000 / day D1-D14 for 4 cycles. After 10 weeks of rest, XELOX-RT regimen x 5 weeks followed by surgery
Other names: Radiotherapy
Time frame: from the signature of Informed Consent up to the end of the study
Time frame: from the signature of Informed Consent up to end of the study
Time frame: from the signature of Informed Consent up to end of the study
Time frame: from the signature of Informed Consent up to end of the study
Sanofi
Industry
Phase II Randomized Trial of Neoadjuvant Chemotherapeutic Treatment (XELOX) Followed by Chemoradiotherapy (XELOX/RT) and Surgery Versus Chemoradiotherapy Followed by Surgery and Chemotherapy in Patients With High Risk Rectal Cancer
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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