EMD 521873 in Advanced Solid Tumors, MTD Finding

PHASE1CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

December 31, 2006

Primary Completion Date

February 28, 2011

Study Completion Date

January 31, 2012

Conditions
Non-Hodgkin Lymphoma
Interventions
BIOLOGICAL

EMD 521873

"Dose escalation steps:~Group 1: 0,075mg/kg - 0,15mg/kg - 0,225mg/kg - 0,3mg/kg - 0,45mg/kg - 0,6mg/kg - 0,9mg/kg (-1,8mg/kg - 2,1mg/kg - 2,5mg/kg - 3,0mg/kg)~Disease control and decision of continuation in patient who benefit from the treatment:~Every second cycle"

BIOLOGICAL

EMD 521873

"Dose escalation steps:~Group 2: CPA plus 0,6mg/kg - 0,9mg/kg~Disease control and decision of continuation in patient who benefit from the treatment:~Every second cycle"

BIOLOGICAL

EMD 521873

"Dose escalation steps:~Group 3: 0,9mg/kg - 1,2mg/kg - 1,5mg/kg (-1,8mg/kg - 2,1mg/kg - 2,5mg/kg - 3,0mg/kg)~Disease control and decision of continuation in patient who benefit from the treatment:~Every second cycle"

Trial Locations (5)

Unknown

Universitäts-Klinikum Mainz III.Medizinische Klinik, Mainz

Medizinische Klinik Universitätsklinikum Mannheim Medizinische Fakultät Mannheim, Mannheim

Istituto Oncologico della Svizzera Italiana Ospedale Regionale Bellinzona e Valli (IOSI), Bellinzona

University of Lausanne Hospitals (CHUV) and Hospitals of Riveria-Chablais, Lausanne

Kantonsspital St. Gallen, Sankt Gallen

All Listed Sponsors
lead

Merck KGaA, Darmstadt, Germany

INDUSTRY

NCT01032681 - EMD 521873 in Advanced Solid Tumors, MTD Finding | Biotech Hunter | Biotech Hunter