A Study to Investigate the Effect of Severely Diminished Liver Function on the Metabolism, Safety, and Tolerability of a Single Oral Dose of Enzalutamide in Men

Severe Hepatic Impairment Clinical Trial

Official title:

A Phase 1, Non-randomized, Open-label, Single-dose Study to Investigate the Pharmacokinetics, Safety and Tolerability of Enzalutamide in Male Subjects With Severe Hepatic Impairment and Normal Hepatic Function

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02138162
• Other study ID #: 9785-CL-0404
• Secondary ID: 2012-004858-29
• Status: Completed
• Phase: Phase 1
• First received: May 12, 2014
• Last updated: May 12, 2014
• Start date: August 2013
• Est. completion date: March 2014

Study information

• Verified date: May 2014
• Source: Astellas Pharma Inc
• Contact: n/a
• Is FDA regulated: No
• Health authority: Bulgaria: Bulgarian Drug AgencyUnited States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The influence of severely diminished liver function on the metabolism, safety, and tolerability of a single oral dose of enzalutamide in a group of 8 men. The results are compared to the data gained from 8 age- and BMI-matched men with normal liver function.

Description:

Screening takes place between Day -22 and Day -2, and subjects are admitted to the clinic on Day -1. Each subject receives a single oral dose of enzalutamide on Day 1, under fasted conditions. They are discharged on Day 7; ambulant visits take place until Day 50. An End of Study Visit (ESV) occurs 7-10 days after the last PK sampling or early withdrawal.

Full PK profiles are obtained for enzalutamide, metabolite 1 of enzalutamide (M1) and metabolite 2 of enzalutamide (M2) up to 1176 hours (Day 50) after administration.

Safety assessments are performed throughout the study. For subjects with severe hepatic impairment, additional Child-Pugh classification and laboratory safety tests (including liver function tests) are performed regularly after administration.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 69 Years

Eligibility

Inclusion Criteria:

• Male subject and their female spouse/partners who are of childbearing potential must be using highly effective contraception consisting of two forms of birth control starting at Screening and continue throughout the study period and for 90 days after the final study drug administration.

• Male subject must not donate sperm starting at Screening and throughout the study period and for 90 days after the final study drug administration.

• Subject has a Body Mass Index (BMI) range of 18.5 - 34.0 kg/m2 inclusive. The subject weighs at least 50 kg [at Screening].

Inclusion Criteria:Subjects with severe hepatic impairment must also meet the following inclusion criteria:

• Subject has a Child-Pugh classification Class C (severe, 10 to 15 points).

Inclusion Criteria: For Healthy Subjects Only:

• Age- and BMI-matched to subjects with severe liver hepatic impairment.

Exclusion Criteria:

• Subject has known or suspected hypersensitivity to enzalutamide, or any components of the formulation used.

• Subject has history of seizure or any condition that may predispose to seizure. Also history of loss of consciousness or transient ischemic attack within 12 months of enrollment (Day 1 visit).

• Subject has used grapefruit (or grapefruit containing products) or marmalade in the week prior to admission to the clinical unit (Day -1), as reported by the subject.

Exclusion Criteria: For Healthy Subjects Only:

• Subject has any of the liver function tests above the upper limit of normal.

Exclusion Criteria: Subjects with severe hepatic impairment must also not have any of the following characteristics:

• Subject has fluctuating or rapidly deteriorating hepatic function, as indicated by strongly varying or worsening of clinical and/or laboratory signs of hepatic impairment within the screening period.

• Subject has surgical porto-systemic shunts, including TIPSS (Trans-jugular intrahepatic portosystemic shunt).

• Subject has presence of severe hepatic encephalopathy (grade > 2).

• Subject has advanced ascites.

• Subject has esophageal variceal bleeding in the medical history (within 6 months before Day -1).

• Subject has thrombocyte level below 40x109 /L and /or hemoglobin below 90 g/L.

• Subject has significant renal dysfunction (creatinine clearance below 50 mL/min, estimated according to the method of Modification of Diet in Renal Disease (MDRD) formula).

• Subject has had previous liver transplantation.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Liver Diseases
• Normal Hepatic Function
• Severe Hepatic Impairment

Intervention

Drug:
• enzalutamide
oral

Locations

Country	Name	City	State
Bulgaria	Comac Medical Ltd.	Sofia

Sponsors (2)

Lead Sponsor	Collaborator
Astellas Pharma Europe B.V.	Medivation, Inc.

Country where clinical trial is conducted

Bulgaria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pharmacokinetics (PK) of enzalutamide after a single oral dose	area under the plasma concentration - time curve (AUC) extrapolated to infinity (AUC0-inf)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No
Primary	PK of enzalutamide after a single oral dose	maximum concentration (observed) (Cmax)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No
Primary	PK of enzalutamide plus N-desmethyl enzalutamide (M2) after a single oral dose	area under the plasma concentration - time curve (AUC) extrapolated to infinity (AUC0-inf)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No
Primary	PK of enzalutamide plus N-desmethyl enzalutamide (M2) after a single oral dose	maximum concentration (observed) (Cmax)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No
Secondary	PK of enzalutamide, M1, M2 and the sum of enzalutamide plus N-desmethyl enzalutamide (M2)	Cmax and AUC0-inf (M1, M2 only), time to attain Cmax (tmax), AUC up to last quantifiable concentration (AUC0-last), apparent terminal elimination half life (t1/2), apparent volume of distribution during the terminal phase after extra vascular dosing (Vz/F), apparent total body clearance after extra vascular dosing (CL/F) (parent compound only), Metabolite-to-Parent Ratio (MPR), percent extrapolated for AUC0-inf (%AUC)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No
Secondary	Additional pharmacokinetic variables for enzalutamide, and, as appropriate, for M1 and M2, based upon unbound plasma concentrations	Unbound Cmax (Cmax,u), unbound AUC0-inf (AUC0-inf,u), and unbound AUC0-last (AUC0-last,u). Unbound CL/F (CLu/F) and unbound Vz/F (Vz,u/F) (parent only)	Days 1-6, 8, 12, 15, 19, 22, 26, 29, 36, 43, 50	No