A Study of GDX012 in Adults With Relapsed or Refractory Acute Myeloid Leukemia

PHASE1/PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

14

Participants

Timeline

Start Date

July 11, 2023

Primary Completion Date

August 19, 2025

Study Completion Date

May 12, 2026

Conditions
Leukemia
Interventions
DRUG

GDX012

GDX012 suspension for IV infusion.

DRUG

Chemotherapy Agents

Chemotherapy agents (fludarabine/cyclophosphamide) as per standard of care.

Trial Locations (14)

77030

MD Anderson Cancer Center, Houston

35205-5802

University of Alabama at Birmingham (UAB) Hospital, Birmingham

91010-3012

City of Hope, Duarte

94304-1812

Stanford University, Palo Alto

80218-1258

Sarah Cannon/CBCI, Denver

60611-3124

Comprehensive Cancer Center of Northwestern University, Chicago

02215

Dana-Farber Cancer Institute, Boston

63110-1010

Washington University, St Louis

14263-0001

Roswell Park Comprehensive Cancer Center, Buffalo

10065-4870

Thomas Jefferson University, New York

44195-0001

Cleveland Clinic, Cleveland

97239-3011

OHSU Knight Cancer Institute, Portland

37203-6521

Tri-Star BMT/Sarah Cannon Nashville, Nashville

53226-3522

Medical College of Wisconsin, Milwaukee

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Takeda

INDUSTRY

NCT05886491 - A Study of GDX012 in Adults With Relapsed or Refractory Acute Myeloid Leukemia | Biotech Hunter | Biotech Hunter