Safety, Dose Tolerance, Pharmacokinetics, and Pharmacodynamics Study of CPX-POM in Patients With Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

January 15, 2018

Primary Completion Date

May 31, 2020

Study Completion Date

May 31, 2020

Conditions
Advanced Solid Tumors
Interventions
DRUG

CPX-POM - 30 mg/m^2

CPX-POM

DRUG

CPX-POM - 60 mg/m^2

CPX-POM

DRUG

CPX-POM - 120 mg/m^2

CPX-POM

DRUG

CPX-POM - 240 mg/m^2

CPX-POM

DRUG

CPX-POM - 360 mg/m^2

CPX-POM

DRUG

CPX-POM - 600 mg/m^2

CPX-POM

DRUG

CPX-POM - 900 mg/m^2

CPX-POM

DRUG

CPX-POM - 1200 mg/m^2

CPX-POM

Trial Locations (5)

34232

Florida Cancer Specialists & Research Institute, Sarasota

37203

Tennessee Oncology PLLC, Nashville

66160

University of Kansas Medical Center, Kansas City

73104

Stephenson Cancer Center, Oklahoma City

80218

Sarah Cannon Research Institute, Denver

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Cmed Clinical Services

OTHER

lead

CicloMed LLC

INDUSTRY

NCT03348514 - Safety, Dose Tolerance, Pharmacokinetics, and Pharmacodynamics Study of CPX-POM in Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter