AEG35156 in Combination With High-dose Cytarabine and Idarubicin in AML Following Failure of a Single Standard Dose Cytarabine Based Frontline Induction Regimen

PHASE2TerminatedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

October 31, 2010

Study Completion Date

October 31, 2010

Conditions
Leukemia
Interventions
DRUG

AEG35156

2 hr infusion of 650 mg of AEG35156 on days 1, 2, 3 and 8. Idarubicin 12 mg/m2 over 30 minutes daily on each of days 4, 5 and 6. The dose of cytarabine will be 1.5 g/m2 daily by continuous infusion x 4 days (days 4-7) in patients under age 65 and x 3 days (days 4-6) in patients age 65 and above.

Trial Locations (18)

10595

New York Medical College, Valhalla

20246

Universitatsklinikum Hamburg-Eppendorf, Hamburg

24116

2. Medizinische Klinik und Poliklinik im Stadtischen Krankenhaus Kile GmgH, Kiel

45147

Universitatsklinimum Essen, Essen

47166

St. Johannes Hospital, Duisburg

48129

Medizinische Klinik a Hamatologie und Onkologie, Münster

55131

III. Medizinische Klinik und Poliklinik der Johannes Gutenberg-Universitat, Mainz

60611

Northwestern University Med School, div. Oncology & Hematology, Chicago

70376

Robert Boasch Krankenhaus Stuttgart, Stuttgart

76502

Cancer Research Institute of Scott & White Hospital, Temple

77303

MD Anderson Cancer Center University of Texas, Houston

80218

Rocky Mountain Blood & Marrow Transplant Program, Denver

90095

UCLA School of Medicine, Los Angeles

Unknown

Princess Margaret Hospital, Toronto

Hopital Maisonneuve-Rosemont, Montreal

Hopital Sacre Coeur, Montreal

J4V 2H1

Hopital Charles Lemoyne, Greenfield Park

09113

Klinikum Chemnitz gGmbH, Chemnitz

Sponsors
All Listed Sponsors
lead

Aegera Therapeutics

INDUSTRY

NCT01018069 - AEG35156 in Combination With High-dose Cytarabine and Idarubicin in AML Following Failure of a Single Standard Dose Cytarabine Based Frontline Induction Regimen | Biotech Hunter | Biotech Hunter