- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04697160
Observational Retrospective Cohort Study of Systemic Therapies for R/R DLBCL (RE-MIND2)
October 12, 2021 updated by: MorphoSys AG
An Observational Retrospective Cohort Study of Systemic Therapies for Relapsed or Refractory Diffuse Large B Cell Lymphoma (R/R DLBCL), to Compare Outcomes to Those From Tafasitamab + Lenalidomide in the L-MIND Study
To compare the efficacy outcomes of the L-MIND cohort with the effectiveness in a matched patient population treated with systemic NCCN/ESMO guideline listed regimens administered in routine clinical care.
Study Overview
Status
Completed
Conditions
Detailed Description
This retrospective observational cohort study aims to generate a historical control consisting of R/R DLBCL patients who received currently guideline recommended therapies.
Study Type
Observational
Enrollment (Actual)
3573
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Adelaide, Australia, 5000
- MorphoSys Research Site
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Benowa, Australia, 4217
- MorphoSys Research Site
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Concord, Australia, 2139
- MorphoSys Research Site
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Darlinghurst, Australia, 2010
- MorphoSys Research Site
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East Melbourne, Australia, 3002
- MorphoSys Research Site
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Fitzroy, Australia, 3065
- MorphoSys Research Site
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Frankston, Australia, 3099
- MorphoSys Research Site
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Kingswood, Australia, 2747
- MorphoSys Research Site
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Nedlands, Australia, 6009
- MorphoSys Research Site
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Leoben, Austria, 8700
- MorphoSys Research Site
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Linz, Austria, 4021
- MorphoSys Research Site
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Salzburg, Austria, 5020
- MorphoSys Research Site
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Sankt Pölten, Austria, 3100
- MorphoSys Research Site
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Wels, Austria, 4600
- MorphoSys Research Site
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Wien, Austria, 1090
- MorphoSys Research Site
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Edmonton, Canada, T6G
- MorphoSys Research Site
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Montréal, Canada, H1T
- MorphoSys Research Site
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Aalborg, Denmark, 9100
- MorphoSys Research Site
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Albi, France, 81000
- MorphoSys Research Site
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Amiens, France, 80054
- MorphoSys Research Site
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Angers, France, 49100
- MorphoSys Research Site
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Caen, France, 14000
- MorphoSys Research Site
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Carcassonne, France, 11010
- MorphoSys Research Site
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Castres, France, 81108
- MorphoSys Research Site
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Chambéry, France, 73000
- MorphoSys Research Site
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Grenoble, France, 38043
- MorphoSys Research Site
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La Roche-sur-Yon, France, 85925
- MorphoSys Research Site
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Lille, France, 59020
- MorphoSys Research Site
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Montpellier, France, 34295
- MorphoSys Research Site
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Narbonne, France, 11100
- MorphoSys Research Site
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Nice, France, 06200
- MorphoSys Research Site
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Nîmes, France, 30029
- MorphoSys Research Site
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Orléans, France, 45100
- MorphoSys Research Site
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Paris, France, 75015
- MorphoSys Research Site
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Paris, France, 75013
- MorphoSys Research Site
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Perpignan, France, 66000
- MorphoSys Research Site
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Pessac, France, 33600
- MorphoSys Research Site
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Pierre-Bénite, France, 69495
- MorphoSys Research Site
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Quimper, France, 29107
- MorphoSys Research Site
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Rodez, France, 12027
- MorphoSys Research Site
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Rouen, France, 76031
- MorphoSys Research Site
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Saint-Brieuc, France, 22027
- MorphoSys Research Site
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Saint-Priest-en-Jarez, France, 42271
- MorphoSys Research Site
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Saint-Quentin, France, 02321
- MorphoSys Research Site
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Toulouse, France, 31100
- MorphoSys Research Site
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Tours, France, 37044
- MorphoSys Research Site
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Troyes, France, 10003
- MorphoSys Research Site
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Vandœuvre-lès-Nancy, France, 54500
- MorphoSys Research Site
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Aschaffenburg, Germany, 63739
- MorphoSys Research Site
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Augsburg, Germany, 86152
- MorphoSys Research Site
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Bad Liebenwerda, Germany, 04924
- MorphoSys Research Site
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Donauwörth, Germany, 86609
- MorphoSys Research Site
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Dresden, Germany, 01127
- MorphoSys Research Site
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Dresden, Germany, 01307
- MorphoSys Research Site
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Flensburg, Germany, 24939
- MorphoSys Research Site
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Frechen, Germany, 50226
- MorphoSys Research Site
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Freiburg im Breisgau, Germany, 79106
- MorphoSys Research Site
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Göttingen, Germany, 37073
- MorphoSys Research Site
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Halle, Germany, 06120
- MorphoSys Research Site
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Hamburg, Germany, 22081
- MorphoSys Research Site
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Hannover, Germany, 30161
- MorphoSys Research Site
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Hannover, Germany, 30171
- MorphoSys Research Site
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Heidelberg, Germany, 69115
- MorphoSys Research Site
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Heilbronn, Germany, 74078
- MorphoSys Research Site
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Köln, Germany, 51103
- MorphoSys Research Site
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Landshut, Germany, 84036
- MorphoSys Research Site
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Lebach, Germany, 66822
- MorphoSys Research Site
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Lübeck, Germany, 23538
- MorphoSys Research Site
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Mainz, Germany, 55131
- MorphoSys Research Site
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Münster, Germany, 48149
- MorphoSys Research Site
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Neustadt, Germany, 31535
- MorphoSys Research Site
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Oldenburg, Germany, 26121
- MorphoSys Research Site
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Oldenburg In Holstein, Germany, 23758
- MorphoSys Research Site
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Potsdam, Germany, 14467
- MorphoSys Research Site
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Ratingen, Germany, 40878
- MorphoSys Research Site
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Saarbrücken, Germany, 66113
- MorphoSys Research Site
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Schorndorf, Germany, 73614
- MorphoSys Research Site
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Stuttgart, Germany, 70376
- MorphoSys Research Site
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Villingen Schwenningen, Germany, 78052
- MorphoSys Research Site
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Villingen-Schwenningen, Germany, 78052
- MorphoSys Research Site
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Wilhelmshaven, Germany, 26389
- MorphoSys Research Site
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Wolfsburg, Germany, 38440
- MorphoSys Research Site
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Alessandria, Italy, 15100
- MorphoSys Research Site
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Ancona, Italy, 60126
- MorphoSys Research Site
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Aviano, Italy, 33081
- MorphoSys Research Site
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Bergamo, Italy, 24127
- MorphoSys Research Site
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Bologna, Italy, 40138
- MorphoSys Research Site
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Como, Italy, 22100
- MorphoSys Research Site
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Cremona, Italy, 26100
- MorphoSys Research Site
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Firenze, Italy, 50134
- MorphoSys Research Site
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Lecce, Italy, 73100
- MorphoSys Research Site
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Milano, Italy, 20132
- MorphoSys Research Site
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Modena, Italy, 41124
- MorphoSys Research Site
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Napoli, Italy, 80131
- MorphoSys Research Site
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Palermo, Italy, 90146
- MorphoSys Research Site
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Perugia, Italy, 06129
- MorphoSys Research Site
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Piacenza, Italy, 29121
- MorphoSys Research Site
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Ponderano, Italy, 13875
- MorphoSys Research Site
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Ravenna, Italy, 48121
- MorphoSys Research Site
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Reggio Calabria, Italy, 89124
- MorphoSys Research Site
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Rimini, Italy, 47923
- MorphoSys Research Site
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Roma, Italy, 00128
- MorphoSys Research Site
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Roma, Italy, 00161
- MorphoSys Research Site
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Roma, Italy, 00189
- MorphoSys Research Site
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Terni, Italy, 05100
- MorphoSys Research Site
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Udine, Italy, 33100
- MorphoSys Research Site
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Vicenza, Italy, 36100
- MorphoSys Research Site
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Busan, Korea, Republic of, 49201
- MorphoSys Research Site
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Busan, Korea, Republic of, 49241
- MorphoSys Research Site
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Seoul, Korea, Republic of, 3080
- MorphoSys Research Site
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Seoul, Korea, Republic of, 5505
- MorphoSys Research Site
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Seoul, Korea, Republic of
- MorphoSys Research Site
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Ulsan, Korea, Republic of, 44033
- MorphoSys Research Site
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Badalona, Spain, 08916
- MorphoSys Research Site
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Barcelona, Spain, 08035
- MorphoSys Research Site
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Hospitalet de Llobregat, Spain, 08908
- MorphoSys Research Site
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Lugo, Spain, 27003
- MorphoSys Research Site
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Madrid, Spain, 28040
- MorphoSys Research Site
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Madrid, Spain, 28007
- MorphoSys Research Site
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Madrid, Spain, 28023
- MorphoSys Research Site
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Madrid, Spain, 28050
- MorphoSys Research Site
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Madrid, Spain, 28006
- MorphoSys Research Site
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Majadahonda, Spain, 28222
- MorphoSys Research Site
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Palma De Mallorca, Spain, 07120
- MorphoSys Research Site
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Palma De Mallorca, Spain, 07198
- MorphoSys Research Site
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Pamplona, Spain, 31008
- MorphoSys Research Site
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Pozuelo De Alarcón, Spain, 28223
- MorphoSys Research Site
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Sabadell, Spain, 08208
- MorphoSys Research Site
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Salamanca, Spain, 37007
- MorphoSys Research Site
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Santander, Spain, 39008
- MorphoSys Research Site
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Sevilla, Spain, 41013
- MorphoSys Research Site
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Valencia, Spain, 46015
- MorphoSys Research Site
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Valencia, Spain, 46026
- MorphoSys Research Site
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Valladolid, Spain, 47003
- MorphoSys Research Site
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Valladolid, Spain, 47012
- MorphoSys Research Site
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Taichung, Taiwan, 40705
- MorphoSys Research Site
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Tainan, Taiwan, 71004
- MorphoSys Research Site
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Taipei city, Taiwan, 100
- MorphoSys Research Site
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Brighton, United Kingdom, BN2
- MorphoSys Research Site
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Manchester, United Kingdom, M20
- MorphoSys Research Site
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Sunderland, United Kingdom, SR4
- MorphoSys Research Site
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Taunton, United Kingdom, TA1
- MorphoSys Research Site
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Truro, United Kingdom, TR1
- MorphoSys Research Site
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Westcliff-on-Sea, United Kingdom, SS0
- MorphoSys Research Site
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Arizona
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Scottsdale, Arizona, United States, 85258
- MorphoSys Research Site
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California
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Clovis, California, United States, 93611
- MorphoSys Research Site
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Los Angeles, California, United States, 90015
- MorphoSys Research Site
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Orange, California, United States, 92868
- MorphoSys Research Site
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Torrance, California, United States, 90502
- MorphoSys Research Site
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Colorado
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Broomfield, Colorado, United States, 80021
- MorphoSys Research Site
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Illinois
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Chicago, Illinois, United States, 60637
- MorphoSys Research Site
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Skokie, Illinois, United States, 60077
- MorphoSys Research Site
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Indiana
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Indianapolis, Indiana, United States, 46260
- MorphoSys Research Site
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Kansas
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Wichita, Kansas, United States, 67214
- MorphoSys Research Site
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Michigan
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Ann Arbor, Michigan, United States, 48109
- MorphoSys Research Site
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Minnesota
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Minneapolis, Minnesota, United States, 55455
- MorphoSys Research Site
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Rochester, Minnesota, United States, 55905
- MorphoSys Research Site
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Mississippi
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Jackson, Mississippi, United States, 39216
- MorphoSys Research Site
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New Jersey
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Morristown, New Jersey, United States, 07960
- MorphoSys Research Site
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New York
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New York, New York, United States, 10029
- MorphoSys Research Site
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New York, New York, United States, 10075
- MorphoSys Research Site
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North Carolina
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Charlotte, North Carolina, United States, 28204
- MorphoSys Research Site
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Oregon
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Portland, Oregon, United States, 97239
- MorphoSys Research Site
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Tennessee
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Nashville, Tennessee, United States, 37232
- MorphoSys Research Site
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Utah
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Salt Lake City, Utah, United States, 84112
- MorphoSys Research Site
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Washington
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Spokane, Washington, United States, 99218
- MorphoSys Research Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with relapsed or refractory DLBCL
Description
Eligibility Criteria:
- Age ≥ 18 years at the initial DLBCL diagnosis.
- One of the following histologically confirmed diagnosis: DLBCL not otherwise specified (NOS); T-cell/histiocyte rich large B-cell lymphoma (THRLBCL); Epstein-Barr virus (EBV) positive DLBCL of the elderly (EBV-positive DLBCL), Grade 3b Follicular Lymphoma (FL), Composite lymphoma with a DLBCL component with a subsequent DLBCL relapse, according to the Revised European American Lymphoma/World Health Organization (REAL/WHO) classification. Additionally, patients with the evidence of histological transformation to DLBCL from an earlier diagnosis of low grade lymphoma (i.e., an indolent pathology such as FL, marginal zone lymphoma, chronic lymphocytic leukemia) into DLBCL with a subsequent DLBCL relapse are also eligible.
- Relapsed or refractory DLBCL and received at least 2 systemic regimens for the treatment of DLBCL, including at least 1 anti-CD20 containing therapy.
Non-Eligibility Criteria:
- Patients with central nervous system (CNS) involvement by lymphoma at initial DLBCL diagnosis.
- Patients who were treated with CD19-targeted therapy or immunomodulatory drugs (IMiDs) (e.g., thalidomide, LEN) as a frontline DLBCL therapy.
- Patients who underwent an allogeneic stem cell transplant.
Patients who had a prior history of malignancies other than DLBCL, unless the patient has been free of the disease for ≥5 years prior to inclusion.
Note: Patients with the following malignancies within the 5 years period are still eligible:
- basal cell carcinoma of the skin
- squamous cell carcinoma of the skin
- carcinoma in situ of the cervix
- carcinoma in situ of the breast
- carcinoma in situ of the bladder
- incidental histological finding of prostate cancer (Tumor/Node/Metastasis [TNM] stage of T1a or T1b)
- Patients who received tafasitamab.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Patients who received systemic therapies for R/R DLBCL
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Overall Survival (OS)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Overall/Objective Response Rate (ORR)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Complete Response Rate (CR)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Duration of Response (DoR)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Event Free Survival (EFS)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Progression Free Survival (PFS)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Time to next treatment (TTNT)
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Treatment discontinuation rate due to adverse events
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Duration of treatment exposure
Time Frame: through study completion, an average of 1 year
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through study completion, an average of 1 year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Eva Waltl, MorphoSys AG
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
April 1, 2020
Primary Completion (ACTUAL)
May 7, 2021
Study Completion (ACTUAL)
May 7, 2021
Study Registration Dates
First Submitted
December 23, 2020
First Submitted That Met QC Criteria
January 5, 2021
First Posted (ACTUAL)
January 6, 2021
Study Record Updates
Last Update Posted (ACTUAL)
October 20, 2021
Last Update Submitted That Met QC Criteria
October 12, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MOR208C213
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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