Status:
COMPLETED
A Study of Orally Administered Pimodivir in Adult Participants With Hepatic Impairment
Lead Sponsor:
Janssen-Cilag International NV
Conditions:
Hepatic Impairment
Eligibility:
All Genders
18-79 years
Phase:
PHASE1
Brief Summary
The purpose is to evaluate the pharmacokinetics (PK) of a single oral dose of 600 milligram (mg) pimodivir in adult participants with impaired hepatic function compared to adult participants with norm...
Eligibility Criteria
Inclusion
- Participant must have a stable hepatic function as confirmed by albumin levels, prothrombin time (PT), International Normalized Ratio (INR), and platelet count measured during screening and those measured within 24 hours prior to study drug administration. Participants with a Transjugular Intrahepatic Portosystemic Shunt procedure will be allowed to participate in the study
- Participant must have a body mass index (BMI; weight \[Kilogram {kg}/height\^2 \[meter {m}\^2\]) between 18.0 and 38.0 kg/m\^2, extremes included, and body weight not less than 50 kg at screening
- Participant must have a 12-lead electrocardiogram (ECG) consistent with normal cardiac conduction and function at screening, including: (a) Sinus rhythm; (b) Pulse rate between 45 and 100 beats per minute (bpm); (c) QT interval corrected for heart rate (QTc) according to Fridericia formula (QTcF) less than or equal to (\<=) 450 millisecond (ms) for male participant and \<= 470 ms for female participant; (d) QRS interval of less than (\<) 120 ms; (e) PR interval \<= 220 ms and (f) Electrocardiogram morphology consistent with healthy cardiac conduction and function. Participant with pacemaker is eligible as long as all criteria mentioned above are met
- 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
- Contraceptive use by men or women should be consistent with local regulations regarding the use of contraceptive methods for participants participating in clinical studies
Exclusion
- Participant has known allergies, hypersensitivity, or intolerance to pimodivir or its excipients
- Participant has donated blood or blood products or had substantial loss of blood (more than 500 milliliter \[mL\]) within 3 months before administration of the study drug or intention to donate blood or blood products during the study
- Participant has received an experimental drug (including investigational vaccines) or used an experimental medical device within 1 month or within a period less than 10 times the drug's half-life, whichever is longer, before administration of the study drug is scheduled
- Participant has preplanned surgery or procedures that would interfere with the conduct of the study
- Participant is a woman who is pregnant, breast-feeding, or planning to become pregnant while enrolled in this study or a woman of childbearing potential who is unwilling to use an acceptable method of contraception
Key Trial Info
Start Date :
May 28 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 27 2020
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT03816631
Start Date
May 28 2019
End Date
April 27 2020
Last Update
February 3 2025
Active Locations (2)
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1
CRS Clinical Research Services Kiel GmbH
Kiel, Germany, 24105
2
APEX GmbH
München, Germany, 81241