A Multicenter, Randomized Double-blind Placebo Controlled Phase III Study of the Efficacy of Xaliproden in Preventing the Neurotoxicity of Oxaliplatin in First-line Treatment of Patients With Metastatic Colorectal Cancer Treated With Oxaliplatin / 5-FU/LV

CompletadoFase 3ClinicalTrials.gov

ID: NCT00305188Tipo: INTERVENTIONALInicio: 1 de dic de 2005Fin estimado: 1 de oct de 2009

Traducción no disponible, mostrando original

Resumen

Primary Objective : Compare the risk of occurrence of Grade3-4 cumulative peripheral sensory neuropathy (PSN) relative to cumulative dose of oxaliplatin between treatment group and placebo group. Main Secondary Objective : Compare the response rate (RR) between treatment group and placebo group in order to ensure that the efficacy of the chemotherapy is not compromised by the addition of xaliproden to the chemotherapeutic regimen. Other Secondary Objectives : study of the neurotoxicity parameters (Duration of oxaliplatin-induced PSN (G2,3,4); overall incidence of PSN during treatment; dose of onset of PSN ; incidence of dose-reduction and dose delay due to PSN; incidence of oxaliplatin treatment discontinuation due to PSN; change in Nerve Conduction Studies (NCS)) ; study of the safety profile (other than PSN) ; study of the chemotherapy efficacy (progression free survival, overall survival).

Elegibilidad

Edad mínima: 18 YearsSexo: ALL

Criterios de inclusión

Measurable disease.
Histologically or cytologically-proven metastatic cancer of the colon or rectum.
Metastatic disease not amenable to potentially curative treatment (eg: inoperable metastatic disease).
Male or female aged \>18 years.
WHO Performance Status (PS) : 0 or 1.
No prior chemotherapeutic regimen for metastatic disease.
Disease-free interval from end of adjuvant therapy of at least 6 months (1 year if oxaliplatin was part of the adjuvant therapy).
Prior radiotherapy is permitted if it was not administered to target lesions identified for this study - unless progression within the radiation portal is documented - and provided it has been completed at least 3 weeks before randomization.
Signed written informed consent prior to study entry.

Criterios de exclusión

Any condition or past medical history that contra-indicates treatment with oxaliplatin and 5-FU, as reported in approved labeling information.
Received chemotherapeutic agents other than 5-FU, LV, Levamisole, irinotecan, capecitabine, oxaliplatin as part of adjuvant therapy.
Peripheral neuropathy \>Grade 1.
Concomitant treatments with drugs/ingredients reported to have a potential activity in preventing peripheral sensory neuropathy.
Concurrent active cancer originating from a primary site other than colon or rectum.
Presence of any symptom suggesting brain metastasis.

Intervenciones

drug

Xaliproden (SR57746A)

oral administration

drug

Placebo

oral administration

drug

Oxaliplatin

IV administration

drug

5-Fluorouracil

IV administration

drug

Leucovorin

IV administration

Ubicaciones

Sanofi-Aventis Administrative Office

Buenos Aires, Argentina

Patrocinadores

PrincipalSanofi

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