Preemptive Therapy for High Risk Chronic Lymphoid Leukemia Stage a

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

82

Participants

Timeline

Start Date

May 22, 2019

Primary Completion Date

January 1, 2022

Study Completion Date

April 24, 2030

Conditions
Chronic Lymphoid Leukemia
Interventions
DRUG

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)."

Trial Locations (23)

14033

CHU CAEN, Caen

25000

Hopitaljean Minjoz, Besançon

33076

Institut Bergonie, Bordeaux

33604

Bordeaux Pessac, Pessac

34500

Ch Beziers, Béziers

35510

Hôpital Privé Sévigné, Cesson-Sévigné

37044

Hôpital Bretonneau - Hématologie et Thérapie Cellulaire, Tours

38043

Chu Grenoble, Grenoble

41000

CH BLOIS, Blois

49933

Chu Angers, Angers

57085

Centre Hospitalier Regional Metz Thionville, Metz

59037

Hopital Huriez, Lille

63000

Chu Estaing, Clermont-Ferrand

64109

Ch Cote Basque, Bayonne

69008

Centre leon berard, Lyon

69495

Centre Hospitalier Lyon Sud, Pierre-Bénite

72000

Chd Le Mans, Le Mans

74374

Ch Annecy, Annecy

76038

Centre Henri Becquerel - Service Hématologie Clinique, Rouen

80054

Chu Amiens, Amiens

85925

Chd Vendee, La Roche-sur-Yon

94000

Chu Creteil, Créteil

130009

Institut Paoli Calmette, Marseille

All Listed Sponsors
lead

French Innovative Leukemia Organisation

OTHER