Efficacy and Safety of BST-236 in Newly Diagnosed Acute Myeloid Leukemia Patients, Unfit for Standard Induction Therapy

PHASE2CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

August 14, 2018

Primary Completion Date

March 16, 2023

Study Completion Date

March 16, 2023

Conditions
Acute Myeloid Leukemia
Interventions
DRUG

BST-236

1 to 4 courses

Trial Locations (16)

10065

Memorial Sloan Kettering Cancer Center New York, New York

19104

Abramson Cancer Center, Philadelphia

29425

Hollings Cancer Center, Charleston

30912

Augusta University Georgia Cancer Center, Augusta

43210

Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Columbus

46237

Franciscan Physician Network Oncology and Hematology Specialists, Indianapolis

48109

University of Michigan Comprehensive Cancer Center, Ann Arbor

49100

Rabin Medical Center, Petah Tikva

60611

Northwestern Memorial Hospital, Chicago

75246

Baylor Scott & White Research Institute Dallas Texas, Dallas

4655202

Rambam medical center hematology department, Haifa

6423906

Tel Aviv Sourasky Medical Center, Tel Aviv

98109-4433

Seattle Cancer Care Alliance, Seattle

26506-9162

West Virginia University, Morgantown

PO Box 151

Soroka University Medical Center, Beersheba

P.O.B 3235

Shaare Zedek Medical Center, Jerusalem

All Listed Sponsors
lead

BioSight Ltd.

INDUSTRY

NCT03435848 - Efficacy and Safety of BST-236 in Newly Diagnosed Acute Myeloid Leukemia Patients, Unfit for Standard Induction Therapy | Biotech Hunter | Biotech Hunter