A Study of Orally Administered Pimodivir in Adult Participants With Renal Impairment

NCT ID: NCT03947814

Last Updated: 2025-02-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 29 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-07-02
• Study Completion Date: 2020-09-09

Brief Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) of pimodivir after a single oral dose of 600 milligrams (mg) in adult participants with severe renal impairment who are not on dialysis and in adult participants with end-stage renal disease (ESRD) who are not yet on dialysis compared to adult participants with normal renal function (Part A). Optionally, to evaluate the PK in adult participants with mild and/or moderate renal impairment compared to adult participants with normal renal function (Part B).

Conditions

Kidney Failure, Chronic

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Part A: Normal renal function (control group)

Participants with normal renal function (glomerular filtration rate \[GFR\] greater than or equal to \[\>=\] 90 milliliters per minute \[mL/min\]) will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Group Type: EXPERIMENTAL

Pimodivir

Intervention Type: DRUG

Participants will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Part A: Severe renal impairment or ESRD

Participants with severe renal impairment (GFR \>=15 to less than \[\<\]30 mL/min) who are not on dialysis or end stage renal disease (ESRD) (GFR \<15 mL/min) not yet on dialysis will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Group Type: EXPERIMENTAL

Pimodivir

Intervention Type: DRUG

Participants will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Part B (Optional): Mild renal impairment

Participants with mild renal impairment (GFR \>=60 mL/min to \<90 mL/min) will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Group Type: EXPERIMENTAL

Pimodivir

Intervention Type: DRUG

Participants will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Part B (Optional): Moderate renal impairment

Participants with moderate renal impairment (GFR \>=30 to \<60 mL/min) will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Group Type: EXPERIMENTAL

Pimodivir

Intervention Type: DRUG

Participants will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Interventions

Pimodivir

Participants will receive single oral dose of 600 mg pimodivir as 2\*300 mg tablets.

Intervention Type: DRUG

Other Intervention Names

JNJ-63623872

Eligibility Criteria

Inclusion Criteria

• Participant must have a body mass index (Body Mass Index [BMI]; body weight (Kilograms per height^2 [kg/m^2]) between 18.0 and 38.0 kg/m^2, inclusive, and body weight not less than 50 kg, inclusive, at screening
• Participants with normal renal function must have normal values for alanine aminotransferase (ALT) and aspartate aminotransferase (AST) (less than or equal to [<=]1.5*upper limit of laboratory normal range [ULN]) at screening and Day -1 and participants with renal impairment and end-stage renal disease (ESRD) must have values for ALT and AST <=3.0*ULN at screening and Day -1
• Participants with normal renal function must have glomerular filtration rate (GFR) greater than or equal to (>=) 90 milliliters per minute (mL/min) and participants with renal impairment (mild, moderate and severe) and ESRD must have >=60 mL/min to <90 mL/min (for Mild renal impairment); >=30 to <60 mL/min (for Moderate renal impairment); >=15 mL/min to <30 mL/min (for Severe renal impairment not on dialysis); and <15 mL/min (for ESRD not on dialysis)
• Participants with normal renal function must have a systolic blood pressure (after the participant is supine for 5 minutes) between 90 millimeters of mercury (mmHg), extremes included, and diastolic blood pressure no higher than 90 mmHg and participants with renal impairment (mild, moderate and severe) and ESRD must have a systolic blood pressure (after the participant is supine for 5 minutes) between 90 and 159 mmHg, extremes included, and diastolic blood pressure no higher than 99 mmHg. If blood pressure is out of range, 1 repeated assessment is permitted after an additional 5 minutes of rest
• A woman, except if postmenopausal, must have a negative highly sensitive serum pregnancy test (beta human chorionic gonadotropin [beta hCG]) at screening and a negative urine pregnancy test on Day -1

Exclusion Criteria

• Participant has any surgical or medical condition that potentially may alter the absorption, metabolism, or excretion of the study drug (for example [e.g.], Crohn's disease), with the exception of renal impairment
• Participant has a history of hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibody or any other clinically active liver disease at screening
• Participant has a history of clinically significant drug allergy such as, but not limited to, sulfonamides and penicillin, or drug allergy diagnosed in previous studies with experimental drugs
• Participant has known allergies, hypersensitivity, or intolerance to pimodivir or its excipients
• Participant has evidence of an active infection

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 79 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Janssen-Cilag International NV

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Janssen-Cilag International NV Clinical Trial

Role: STUDY_DIRECTOR

Janssen-Cilag International NV

Locations

CRS Clinical Research Services Kiel GmbH

Kiel, , Germany

APEX GmbH

München, , Germany

Countries

Germany

Other Identifiers

63623872FLZ1014

Identifier Type: OTHER

Identifier Source: secondary_id

2018-002818-12

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CR108616

Identifier Type: -

Identifier Source: org_study_id