Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02269579

Pharmacokinetic and Pharmacodynamic Assessment of Treatment With CPX-351 (Cytarabine: Daunorubicin) Liposome for Injection in Acute Leukemias and MDS Patients With Moderate Hepatic Impairment

An Open Label Phase II Pharmacokinetic and Pharmacodynamic Assessment of Treatment With CPX-351 (Cytarabine: Daunorubicin) Liposome for Injection in Acute Leukemias and MDS Patients With Moderate Hepatic Impairment

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Jazz Pharmaceuticals · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To assess the impact of moderate hepatic impairment on cytarabine and daunorubicin pharmacokinetics and their metabolites following administration of CPX-351.

Conditions

Interventions

TypeNameDescription
DRUGCPX-351

Timeline

Start date
2015-04-01
Primary completion
2017-06-01
Completion
2017-06-01
First posted
2014-10-21
Last updated
2018-03-14

Locations

5 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02269579. Inclusion in this directory is not an endorsement.

Pharmacokinetic and Pharmacodynamic Assessment of Treatment With CPX-351 (Cytarabine: Daunorubicin) Liposome for Injecti (NCT02269579) · Clinical Trials Directory