drugset / Trial / NCT01991678

A Study in Cancer Patients With Hepatic Impairment to Evaluate the Pharmacokinetics and Safety of NKTR-102 (Etirinotecan Pegol)

NCT01991678

Phase 1 Completed 25 enrolled Nektar Therapeutics
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate the PK and safety of NKTR-102 in patients with mild, moderate, or severe hepatic impairment.

Timeline

Start
2013-11
Primary completion
2017-05
Completion
2017-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Etirinotecan Pegol Other / unclassified 50 mg/m2 Intravenous
Subject Etirinotecan Pegol Other / unclassified 120 mg/m2 Intravenous
Subject Etirinotecan Pegol Other / unclassified 145 mg/m2 Intravenous

Indications

No indication recorded.