A Trial to Evaluate the Potential Impact of Renal Impairment on the Pharmacokinetics and Safety of CPX-351

PHASE1CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

November 20, 2018

Primary Completion Date

May 26, 2021

Study Completion Date

May 26, 2021

Conditions
Hematologic MalignancyAcute Myeloid LeukemiaAcute Lymphocytic LeukemiaAcute Lymphoblastic LeukemiaMyelodysplastic Syndromes
Interventions
DRUG

CPX-351

CPX-351 is administered as an intravenous (IV) infusion over approximately 90 minutes.

DRUG

CPX-351

CPX-351 is administered as an intravenous (IV) infusion over approximately 90 minutes.

Trial Locations (13)

10021

Weill Cornell Medical College, New York

10595

New York Medical/Westchester, Valhalla

20007

Georgetown University Medical Center, Washington D.C.

27157

Wake Forest Baptist Health, Winston-Salem

30342

Northside Hospital - Blood and Bone Marrow Transplant Group of Georgia, Atlanta

53226

Medical College of Wisconsin, Milwaukee

66205

University of Kansas Cancer Center, Westwood

75246

Baylor University Medical Center, Dallas

97239

Oregon Health and Science University, Portland

98109

Fred Hutchinson Cancer Research Center, Seattle

07601

Hackensack University Medical Center, Hackensack

V5Z 1M9

Vancouver General Hospital, Vancouver

M5G 1Z5

University Health Network/Princess Margaret Cancer Center, Toronto

Sponsors
All Listed Sponsors
lead

Jazz Pharmaceuticals

INDUSTRY