Safety Study to Assess AFM11 in Patients With Relapsed or Refractory Adult B-precursor ALL

PHASE1TerminatedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

September 30, 2018

Study Completion Date

April 30, 2019

Conditions
Leukemia, B-Cell
Interventions
DRUG

AFM11

Accelerated-titration dose-escalation with 1 patient per dose-level, followed by standard dose-escalation (3 + 3 design), Treatment duration: 2 weeks

Trial Locations (12)

197022

First Pavlov State Medical University, Saint Petersburg

Unknown

LKH-Universitätsklinikum Graz, Graz

Kepler Universitätsklinikum Linz, Linz

Uniklinikum Salzburg, Salzburg

University Hospital, Brno

Rambam Medical Center, Haifa

Hadassah Medical Center, Jerusalem

Rabin Medical Center, Petah Tikva

Independent Public Healthcare Municipal Hospital, Chorzów

University Hospital, Krakow

Baranov Republican Hospital, Petrozavodsk

Almazov NW Federal Medical Research Center, Saint Petersburg

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Affimed GmbH

INDUSTRY

NCT02848911 - Safety Study to Assess AFM11 in Patients With Relapsed or Refractory Adult B-precursor ALL | Biotech Hunter | Biotech Hunter