82
Participants
Start Date
May 22, 2019
Primary Completion Date
January 1, 2022
Study Completion Date
April 24, 2030
Venetoclax
"Venetoclax is administered according to the usual schedule an escalating dose from 20 milligram per day the first week, then 50 milligram per day the second week, 100 milligram per day the third week, 200 milligram per day the fourth week and then 400 milligram per day.~* For patient achieving a Compete Response with Minimal Residual Disease inferior to 0,01 percent in bone marrow at month 12, treatment will be stopped at month18 (18 months for total duration of treatment ).~* For responding patients at month12 (Complete Response or Partial Response) with bone marrow Minimal Residual Disease inferior to 0.01 percent, treatment will be continued until month 24 (24 months for total duration of treatment)."
CHU CAEN, Caen
Hopitaljean Minjoz, Besançon
Institut Bergonie, Bordeaux
Bordeaux Pessac, Pessac
Ch Beziers, Béziers
Hôpital Privé Sévigné, Cesson-Sévigné
Hôpital Bretonneau - Hématologie et Thérapie Cellulaire, Tours
Chu Grenoble, Grenoble
CH BLOIS, Blois
Chu Angers, Angers
Centre Hospitalier Regional Metz Thionville, Metz
Hopital Huriez, Lille
Chu Estaing, Clermont-Ferrand
Ch Cote Basque, Bayonne
Centre leon berard, Lyon
Centre Hospitalier Lyon Sud, Pierre-Bénite
Chd Le Mans, Le Mans
Ch Annecy, Annecy
Centre Henri Becquerel - Service Hématologie Clinique, Rouen
Chu Amiens, Amiens
Chd Vendee, La Roche-sur-Yon
Chu Creteil, Créteil
Institut Paoli Calmette, Marseille
French Innovative Leukemia Organisation
OTHER