A Phase 2 Open-Label Multicenter Study Of The Garft Inhibitor AG2037 In Patients With Metastatic Colorectal Cancer Who Failed Treatment With A 5-Fluorouracil/Leucovorin Regimen.
Colección de datos
Enfermedades del colon+8
+ Enfermedades del Sistema Digestivo
+ Neoplasias del sistema digestivo
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de diciembre de 2003
Fecha en la que se inscribió al primer participante.To determine the response rate in patients with metastatic colorectal cancer who failed treatment with a 5-Fluorouracil/Leucovorin regimen and up to one other chemotherapeutic regimen (not including adjuvant chemotherapy).
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 56 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: * Histologically or cytologically confirmed metastatic adenocarcinoma of the colon or rectum * Stage IV or recurrent disease * Measurable disease * Disease progression or recurrence during or after completion of prior first-line chemotherapy with fluorouracil and leucovorin calcium (5-FU/LV) * Prior irinotecan or oxaliplatin as part of the 5-FU/LV regimen or as subsequent therapy allowed * Only 2 prior regimens for metastatic disease allowed * One additional regimen as adjuvant therapy allowed provided patient remained disease-free for \> 6 months after completion of therapy\* * Newer, targeted investigational agents (e.g., cetuximab or bevacizumab) are not counted as a chemotherapeutic regimen unless used in combination with a cytotoxic regimen NOTE: \*If evidence of failure occurred within \< 6 months after completion of adjuvant therapy, patients may have received only 1 additional regimen for metastatic disease * No active brain metastases (requiring treatment or progressing) Exclusion Criteria: * History of blood transfusion within 14 days * Need of concurrent Administration of allopurinol * History of Radiotherapy or Chemotherapy within 4 weeks * Any psychological or sociological condition, addidtive disorder or family problems that might preclude compliance with the protocol * Any unstable or severe intercurrent medical condition that in the opinion of th einvestigator might interfere with achievement of study objectives * Receipt of an investigational agent within 28 days prior to first day of dosing with AG-2037 * Pregnant or breast feeding * Previous treatment with GARFT inhibitors * History of a malignancy (other than colorectal cancer) excpet those treated with curative intent for skin cancer (other than melanoma) or in situ breast or cervical cancer or those treated with curative intent for any other cancer with no evidence of disease for 5 years * Active brain metastases (requiring treatment or progression)
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Objetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene 4 ubicaciones
Pfizer Investigational Site
Washington, United StatesPfizer Investigational Site
Tampa, United StatesPfizer Investigational Site
New York, United States