Blinatumomab in Adult Patients With Minimal Residual Disease (MRD) of B-precursor Acute Lymphoblastic Leukemia

PHASE2CompletedINTERVENTIONAL
Enrollment

83

Participants

Timeline

Start Date

March 15, 2017

Primary Completion Date

August 15, 2021

Study Completion Date

March 10, 2023

Conditions
ALL, Recurrent, Adult
Interventions
DRUG

Blinatumomab

"Patients will receive blinatumomab at a dose of 28 µg/day as continuous intravenous infusion at constant flow rate for four weeks, followed by a two-week infusion free interval, defined as one treatment cycle. Up to of four cycles will be performed.~In case of defined toxicities, the dose of blinatumomab may be reduced to 9µg/day.~Patients with an MRD relapse may qualify to receive additional treatment with blinatumomab."

Trial Locations (22)

60590

University Hospital of Frankfurt (Main), Frankfurt am Main

Unknown

Charité - Campus Benjamin Franklin, Berlin

Uniklinik Dresden, Dresden

Uniklinik Düsseldorf, Düsseldorf

Univeristätsklinikum Essen, Essen

Universitätsklinikum Freiburg, Freiburg im Breisgau

Universitätsmedizin Göttingen, Göttingen

Uniklinik Hamburg Eppendorf, Hamburg

Medizinische Hochschule Hannover, Hanover

Uniklinik Heidelberg, Heidelberg

UKSH-Kiel, Kiel

Universitätsklinik Leipzig, Leipzig

Klinikum Mannheim, Mannheim

Universitätsklinkum Gießen und Marburg, Marburg

Klinikum Großhadern, München

Uniklinik Münster, Münster

Klinikum Nürnberg Nord, Nuremberg

Uniklinik Regensburg, Regensburg

Robert - Bosch - Krankenhaus, Stuttgart

Universitätsklinik Tübingen, Tübingen

Universitätsklinkum Ulm, Ulm

Uniklinik Würzburg, Würzburg

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Goethe University

OTHER