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Spots Global Cancer Trial Database for Evaluation of the Persistence of the Complete Molecular Remission After Stopping Imatinib Chronic Myeloid Leukemia

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Trial Identification

Brief Title: Evaluation of the Persistence of the Complete Molecular Remission After Stopping Imatinib Chronic Myeloid Leukemia

Official Title: Evaluation of the Persistence of the Complete Molecular Remission After Stopping Imatinib Chronic Myeloid Leukemia (STIM)

Study ID: NCT00478985

Interventions

Imatinib ending

Study Description

Brief Summary: The first purpose of this study is to evaluate the persistence of the complete molecular remission in patients with Chronic Myeloid Leukemia after stopping imatinib treatment (determine by Reverse Transcription real-time Polymerase Chain Reaction (RT-PCR) negative for bcr-abl transcripts). The second purpose is to determine clinicals and biologicals factors associated with the persistent complete molecular remission.

Detailed Description: Principal Objective : To evaluate the complete molecular remission persistence after stopping imatinib during six months as measured by RT-PCR negative for bcr-abl transcripts in patients with Chronic Myeloid Leukemia . Secondary Objective : * To determine clinicals factors associated with complete molecular remission before and after stopping imatinib in patients with Chronic Myeloid Leukemia. * To determine the biologics factors (immunologic and molecular) associated with complete molecular remission before and after stopping imatinib in patients with Chronic Myeloid Leukaemia. * To determine the molecular relapse level after more than six month of persistent complete molecular remission without imatinib. * To determine the complete molecular remission length. * To evaluate medical and economical impact of stopping imatinib treatment. Study design : multicentric trial

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University Hospital Angers, Angers Cedex 01, Angers, France

H么pital Henri-Mondor, Creteil, Cr茅teil, France

H么pital Saint Louis, PARIS Cedex, Paris, France

Institut Bergoni茅, BORDEAUX Cedex, , France

University Hospital Bordeaux, Groupe Hospitalier Pellegrin, Bordeaux cedex, , France

H么pital Morvan, Brest, , France

CHU de Grenoble, Grenoble, , France

Centre hospitalier-service de m茅decine interne Onco-H茅matologique, La Roche sur Yon, , France

H么pital Andr茅 Mignot, Le Chesnay Cedex, , France

H么pital Bic锚tre, AP-HP, Le Kremlin-bicetre, , France

H么pital Claude Huriez, Lille, , France

H么pital Edouard Herriot, Lyon, , France

Institut Paoli Calmet, Marseille Cedex 9, , France

CHR de Metz-Thionville, Metz Cedex 01, , France

University Hospital H么tel-Dieu, Nantes, , France

Centre Hospitalier de Nevers, Nevers, , France

University Hospital Nice, Nice, , France

H么pital Necker-Enfants Malades, Paris, , France

Haut L茅v锚que Hospital, Pessac, , France

University Hospital Poitiers, Poitiers, , France

University Hospital Strasbourg, H么pital Civil, Strasbourg, , France

University Hospital Toulouse, Purpan, Toulouse, , France

University Hospital Brabois, Vandoeuvre Les Nancy, , France

Centre Hospitalier Bretagne Atlantique, Vannes, , France

Contact Details

Name: Fran莽ois-Xavier MAHON, MD

Affiliation: University Hospital Bordeaux, France

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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