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A Multicentre, Phase II, Open Label, Single Arm Study of Pixantrone in Patients With CD20-positive Relapsed or Refractory Aggressive Non-Hodgkin Lymphoma Treated With Rituximab, Ifosfamide and Etoposide.
This study will evaluate the efficacy of Pixantrone with rituximab, ifosfamide and etoposide as measured by the overall metabolic response rate after 2 cycles of treatment or at permanent treatment discontinuation.
This study will evaluate the efficacy of Pixantrone with rituximab, ifosfamide and etoposide as measured by the overall metabolic response rate after 2 cycles of treatment or at permanent treatment discontinuation.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
AZ Sint Jan
Bruges, Belgium
Institut Jules Bordet - Centre des tumeurs de l'ULB
Brussels, Belgium
Centre Hospitalier de Jolimont
Haine-Saint-Paul, Belgium
CH d'Avignon
Avignon, France
Centre Hospitalier de la Côte Basque
Bayonne, France
CHU Jean Minjoz
Besançon, France
Hôpital Haut-Lévèque
Bordeaux, France
Centre Hospitalier William Morey
Chalon-sur-Saône, France
Clinique Victor Hugo
Le Mans, France
CHRU de Lille
Lille, France
Start Date
December 26, 2018
Primary Completion Date
December 24, 2024
Completion Date
December 24, 2024
Last Updated
March 10, 2026
74
ACTUAL participants
Pixantrone
DRUG
Ifosfamide
OTHER
Etoposide
OTHER
Rituximab
OTHER
Transplant
PROCEDURE
Lead Sponsor
The Lymphoma Academic Research Organisation
NCT03749018
NCT01787409
Data Source & Attribution
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