A Phase I Study of IGN523 in Subjects With Relapsed or Refractory AML

PHASE1CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

February 28, 2014

Primary Completion Date

March 31, 2015

Study Completion Date

June 30, 2015

Conditions
Acute Myelogenous LeukemiaAcute Myeloid Leukemia
Interventions
DRUG

IGN523

Given intravenously every week for 8 weeks. Dosing beyond 8 weeks will be permitted for subjects meeting criteria for ongoing clinical benefit and acceptable safety.

Trial Locations (6)

30322

Winship Cancer Institute, Emory University, Atlanta

46237

Indiana Blood and Marrow Transplantation Clinic, Indianapolis

48109

University of Michigan Health System, Ann Arbor

77030

MD Anderson Cancer Center, Houston

92037

UCSD Medical Center / Thornton Hospital, La Jolla

98109

University of Washington, Seattle

Sponsors
All Listed Sponsors
lead

Igenica Biotherapeutics, Inc.

INDUSTRY