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Clinical Trials/NCT03864601
NCT03864601
Completed
Phase 1

A Phase 1, Open-label Study to Determine the Absorption, Metabolism, and Routes of Excretion, Following Oral Administration of (14C) Radiolabeled JNJ-56136379 in Healthy Male Subjects

Janssen Research & Development, LLC1 site in 1 country6 target enrollmentStarted: April 9, 2019Last updated:
ConditionsHealthy
Interventions14C-JNJ-56136379

Overview

Phase
Phase 1
Status
Completed
Enrollment
6
Locations
1
Primary Endpoint
AUC(0-last): Ratio of JNJ-56136379 Concentration and Total Radioactivity in Plasma

Overview

Brief Summary

The purpose of this study is to investigate the absorption, the metabolic pathways, the route and rate of elimination, and total recovery of 14C-JNJ-56136379 and/or total drug derived radioactivity in healthy male adult participants after administration of a single oral dose of 14C-JNJ-56136379.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • During the study (from the day of study drug intake onwards) and for a minimum of 1 spermatogenesis cycle (defined as approximately 90 days) after receiving study drug, a male participant: must agree: (a) to wear a condom when engaging in any activity that allows for passage of ejaculate to another person (male participant should also be advised of the benefit for a female partner to use a highly effective method of contraception as condom may break or leak); (b) not to donate sperm for the purpose of reproduction.
  • Contraceptive use should be consistent with local regulations regarding the use of contraceptive methods for participants participating in clinical studies
  • Must have a body mass index (BMI; weight \[kg\]/height\^2 \[m\]\^2) between 18.0 and 30.0 kilogram per meter square (kg/m\^2) (inclusive), and body weight not less than 50 kilogram (kg) at screening
  • Healthy on the basis of physical examination, medical history and surgical history, and vital signs performed at screening. If there are abnormalities, the participant may be included only if the investigator judges the abnormalities to be not clinically significant or to be appropriate and reasonable for the population under study. This determination must be recorded in the participant's source documents and initialed by the investigator
  • Healthy on the basis of clinical laboratory tests performed at screening
  • Must have a normal 12-lead electrocardiogram (ECG) at screening

Exclusion Criteria

  • Any evidence of heart block or bundle branch block at screening
  • Human immunodeficiency virus 1 (HIV-1) or HIV-2 infection (confirmed by antibodies) at screening
  • History of hepatitis A, B, C, or E infection, or current hepatitis A infection (confirmed by hepatitis A antibody immunoglobulin M \[IgM\]), or hepatitis B virus (HBV) infection (confirmed by hepatitis B surface antigen), or hepatitis C virus (HCV) infection (confirmed by HCV antibody), or hepatitis E infection (confirmed by hepatitis E \[HEV\] antibody IgM \[in case HEV IgM positive, a confirmatory HEV ribonuclic acid {RNA} test should be performed\]) at screening
  • Any current, or history of, confirmed clinically significant skin disease requiring intermittent or chronic treatment such as, but not limited to, dermatitis, eczema, drug rash, psoriasis, food allergy, and urticaria
  • A history of clinically significant drug allergy such as, but not limited to, sulfonamides and penicillins, or drug allergy witnessed in previous studies with experimental drugs

Arms & Interventions

14C-JNJ-56136379

Experimental

Participants will receive a single oral 25 milligram (mg) dose of 14C-JNJ-56136379 on Day 1 under fed conditions.

Intervention: 14C-JNJ-56136379 (Drug)

Outcomes

Primary Outcomes

AUC(0-last): Ratio of JNJ-56136379 Concentration and Total Radioactivity in Plasma

Time Frame: Up to 552 hours postdose

Ratio of JNJ-56136379 concentration (plasma) and total radioactivity (plasma) for area under the plasma concentration-time curve from time zero to last quantifiable concentration time (AUC\[0-last\]) will be assessed.

Cmax: Ratio of JNJ-56136379 Concentration and Total Radioactivity in Plasma

Time Frame: Up to 552 hours postdose

Ratio of JNJ-56136379 concentration (plasma) and total radioactivity (plasma) for maximum observed plasma concentration (Cmax) will be assessed.

AUC(0-infinity): Ratio of JNJ-56136379 Concentration and Total Radioactivity in Plasma

Time Frame: Up to 552 hours postdose

Ratio of JNJ-56136379 concentration (plasma) and total radioactivity (plasma) for area under the plasma concentration- time curve from time zero to infinite time (AUC \[0-infinity\]) will be assessed.

Total Recovery of Radioactive Dose in Feces and Urine for 14C-JNJ-56136379

Time Frame: Up to 552 hours postdose

The amount of 14C-JNJ-56136379 recovered from the total administered radioactive dose in the feces and urine will be calculated.

Total Radioactivity in Whole Blood, Plasma, Feces and Urine for 14C-JNJ-56136379

Time Frame: Up to 552 hours postdose

The total radioactivity of 14C-JNJ-56136379 in the whole blood plasma, feces and urine will be calculated.

Secondary Outcomes

  • Area Under the Plasma Concentration-Time Curve from Time Zero to Infinite Time (AUC [0-infinity]) of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Apparent Terminal Elimination Half-Life (t1/2) of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Apparent Terminal Elimination Rate Constant (Lambda[z]) of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Amount of JNJ-56136379 Excreted in Feces (Fe)(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Metabolic Profiles of JNJ-56136379 in Plasma, Urine, and Feces(Predose (Day 1), 1, 2, 4, 8, 24, 48, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Actual Sampling Time to Reach the Maximum Observed Plasma Concentration (Tmax) of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Maximum Observed Plasma Concentration (Cmax) of JNJ-56136379(Predose (Day 1), 1, 2, 4, 8, 24, 48, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Area Under the Plasma Concentration-Time Curve from Time Zero to Last Quantifiable Concentration Time (AUC [0- Last]) of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Amount of JNJ-56136379 Excreted in Urine within the Time Interval t1 to t2 (Ae[t1-t2])(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Amount of JNJ-56136379 Excreted in Urine (Ae)(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Percentage of JNJ-56136379 Excreted in Urine (Ae%dose)(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Percentage of AUC(0-inifinity) (%AUC[0- infinity],ex of JNJ-56136379(Predose (Day 1), 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, 72, 96, 192, 288, 432, 552 hours postdose (Day 24))
  • Amount of JNJ-56136379 Excreted in Feces within the Time Interval t1 to t2 (Fe[t1-t2])(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Percentage of JNJ-56136379 Excreted in Feces (Fe,%dose)(Predose and at every 24-hour interval up to 552 hours (Day 24) postdose)
  • Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability(Approximately up to 2.5 months)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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