Phase IIa Study Evaluating Safety and Efficacy of BL-8040 in Relapsed/Refractory AML Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

April 30, 2013

Primary Completion Date

March 31, 2016

Study Completion Date

July 20, 2023

Conditions
Acute Myeloid Leukemia
Interventions
DRUG

Ara-C

IV (intravenous administration)

DRUG

BL-8040

SC (subcutaneous injection)

Trial Locations (10)

10065

Memorial Sloan-Kettering Cancer Center, New York

21231

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore

31096

Rambam Medical Center, Haifa

32224

Mayo Clinic, Jacksonville

52621

Chaim Sheba Medical Center, Ramat Gan

63110

Washington University School of Medicine, St Louis

64239

Tel-Aviv Sourasky Medical Center, Tel Aviv

77030

MD Anderson Cancer Center, Houston

91031

Shaare Zedek Medical Center, Jerusalem

Unknown

Meir Medical Center, Kfar Saba

Sponsors

Lead Sponsor

All Listed Sponsors
lead

BioLineRx, Ltd.

INDUSTRY

NCT01838395 - Phase IIa Study Evaluating Safety and Efficacy of BL-8040 in Relapsed/Refractory AML Patients | Biotech Hunter | Biotech Hunter