9-ING-41 in Pediatric Patients With Refractory Malignancies.

PHASE1TerminatedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

June 5, 2020

Primary Completion Date

July 7, 2025

Study Completion Date

July 7, 2025

Conditions
Refractory CancerRefractory NeoplasmCancer PediatricRefractory TumorPediatric CancerPediatric Brain TumorNeuroblastomaNeuroblastoma RecurrentPediatric LymphomaPediatric MeningiomaDiffuse Intrinsic Pontine Glioma
Interventions
DRUG

9-ING-41

9-ING-41 will be administered by intravenous infusion twice weekly at an initial dose of 9.3 mg/kg. Cycle duration is 21 days.

DRUG

Irinotecan

Irinotecan 50 mg/m2/day administered over 90 minutes IV on days 1-5 every 21 days.

DRUG

Temozolomide

Temozolomide will be administered at a dose of 100 mg/m2/dose by mouth on Days 1 through 5 of a 21 day cycle.

DRUG

Cyclophosphamide

Cyclophosphamide 400 mg/m2/dose administered intravenously over 30 min on Days 1 through 5 of a 21 day cycle.

DRUG

Topotecan

Topotecan 1.2 mg/m2/dose administered intravenously over 30 min once on Days 1 through 5 of a 21 day cycle.

Trial Locations (9)

27708

Duke Children's Hospital and Health Center, Duke University Medical Center, Durham

28204

Levine Cancer Center, Charlotte

48109

Mott Children's Hospital, Ann Arbor

60637

University of Chicago, Chicago

77030

Texas Children's Hospital, Houston

80045

Children's Hospital Colorado, Aurora

98101

Seattle Children's Research Institute, Seattle

94158-2549

University of California, San Francisco, San Francisco

02912

Brown University, Providence

Sponsors
All Listed Sponsors
lead

Actuate Therapeutics Inc.

INDUSTRY

NCT04239092 - 9-ING-41 in Pediatric Patients With Refractory Malignancies. | Biotech Hunter | Biotech Hunter