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Spots Global Cancer Trial Database for Study With Rituximab-Gemcitabine/Oxaliplatin in Relapsed Indolent Lymphoma

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study With Rituximab-Gemcitabine/Oxaliplatin in Relapsed Indolent Lymphoma

Official Title: Multicentric Phase I/II Study for the Efficacy of a Combination of Rituximab, Gemcitabine and Oxaliplatin in Relapsed/Refractory Indolent Lymphoma

Study ID: NCT00954005

Study Description

Brief Summary: The purpose of the phase I part is to determine the tolerability, the initial safety profile and maximum tolerated dose of oxaliplatin in combination with gemcitabine for indolent lymphoma. In the phase II part the investigators want to estimate the activity of gemcitabine and oxaliplatin in combination with rituximab for patients with relapsed/refractory indolent lymphoma.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Klinikum Ludwigshafen, Ludwigshafen, , Germany

Contact Details

Name: Martin Hoffmann, Dr.

Affiliation: German Low Grade Lymphoma Study Group

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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