Study to Evaluate Efficacy and Tolerance of R-GemOx in DLBCL and MCL

NCT01562977 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2017-10-30

No results posted yet for this study

Summary

The purpose of this study is to determine efficacy of rituximab, gemcitabine, oxaliplatin and dexametasone (R-GemOx) chemotherapy schedule.

Conditions

Interventions

DRUG

Rituximab, Gemcitabine, Oxaliplatin, Dexametasone

until progression or unacceptable toxicity develops, 8 cicles max Rituximab: 375 mg/m2, IV, day 1. Gemcitabine: 1000 mg/m2, IV, day 2. Oxaliplatin: 100 mg/m2, IV, day 2. Dexametasone: 20 mg/day, days 1-3, oral.

Sponsors & Collaborators

  • Grupo Español de Linfomas y Transplante Autólogo de Médula Ósea

    lead OTHER

Principal Investigators

  • Andrés López Hernández, MD · Hospital Vall d´Hebrón

  • Mª Dolores Caballero Barrigón, MD · Hospital Clínico de Salamanca

  • Jorge Gayoso Cruz, MD · Hospital Universitario Gregorio Marañón

  • Juan Alfonso Soler Campos, MD · Corporació Sanitari Parc Taulí

  • Carlos Montalbán Sanz, MD · Hospital Universitario Ramon y Cajal

  • Juan Manuel Sancho Cía, MD · Germans Trias i Pujol Hospital

  • Isidro Jarque, MD · Hospital La Fe de Valencia

  • Secundino Ferrer, MD · Hospital Dr. Peset

  • Carlos Grande, MD · Hospital 12 de Octubre

  • Pilar Martínez Barranco, MD · Fundación Hospital de Alcorcón

  • Miguel Ángel Canales Albendea, MD · Hospital La Paz

  • Jose Antonio García Marco, MD · Hospital Puerta de Hierro de Majadahonda

  • Roberto Hernández Martín, MD · Hospital Virgen de la Concha

  • José Manuel Calvo Villas, MD · Hospital Dr. Jose Molina Orosa

  • Miguel Hernández, García · Hospital Universitario de Canarias

  • Elena Pérez Ceballos, MD · Hospital Morales Meseguer

  • José M. Moraleda Jiménez, MD · Hospital Virgen de la Arrixaca

  • Eulogio Conde García, MD · Hospital Marqués de Valdecilla

  • Carlos Panizo Santos, MD · Clínica Universitaria Navarra

  • Mª Rosario Varela, MD · Complejo Hospitalario A Coruña

  • Jose Luis Bello López, MD · Complejo Hospitalario Universitario de Santiago

  • Maria José Ramírez Sánchez, MD · Hospital del SAS Jerez

  • Luis Palomera, MD · Hospital Clínico Lozano Blesa

  • Pilar Giraldo, MD · Hospital Miguel Servet

  • Antonio Gutiérrez, MD · Hospital Son Espasses

  • Joan Bargay Leonart, MD · Hospital Son Llàtzer

  • Eva González Barca, MD · Hospital Duran i Reynals

  • Javier Briones Meijide, MD · Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2015-04-30
Completion
2015-04-30

Countries

  • Spain

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01562977 on ClinicalTrials.gov