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Clinical Trials/NCT01964651
NCT01964651
Completed
Phase 1

A Double-Blind, Placebo-Controlled, Randomized, Multiple Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42165279 in Healthy Young and Elderly Subjects

Janssen Research & Development, LLC0 sites40 target enrollmentOctober 2013

Overview

Phase
Phase 1
Intervention
JNJ-42165279 50 mg
Conditions
Healthy
Sponsor
Janssen Research & Development, LLC
Enrollment
40
Primary Endpoint
Concentrations in cerebrospinal fluid of JNJ-42165279
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of JNJ-42165279 in healthy, young and elderly, male and female participants after repeated oral dose administration.

Detailed Description

This is a double-blind (neither physician nor participant knows the treatment that the participant receives), randomized (the study drug is assigned by chance), placebo-controlled (an inactive substance is compared with a medication to test whether the medication has a real effect in a clinical study) trial that will be conducted in two parts. Thirty two (32) healthy participants are planned to be included in total, in four cohorts (groups). Participants in each cohort will receive JNJ-42165279 (n=6) or placebo (n=2) once-daily for 10 consecutive days. In Part 1, two cohorts of healthy male participants, 18 to 55 years of age, will be enrolled. Cohort A will receive 50 mg JNJ-42165279 or placebo for 10 days, and Cohort B will receive 30 mg JNJ-42165279 or placebo for 10 days. In Part 2, Cohort C will consist of 8 healthy female participants of non-childbearing potential (surgically sterile or postmenopausal), 18 to 58 years of age, who will receive 100 mg JNJ-42165279 or placebo for 10 days. Cohort D will consist of 8 healthy elderly male or female participants, from 65 to 85 years of age, who will receive 100 mg JNJ-42165279 or placebo for 10 days. The dose may be adapted before each cohort starts based on available data. The maximum dose will not exceed 100 mg once-daily. For all participants, this study will consist of an eligibility screening examination (between 28 and 3 days prior to the first dose administration), a double-blind treatment phase consisting of 2 days before dosing, 10 dosing days (Day 1 to 10), 4 days after dosing (Day 11 to 14), and a follow-up examination (within 7 to 14 days after last dose administration). The total study duration for each participant will not exceed 8 weeks.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
October 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Body Mass Index (BMI) between 18 and 30 kg/m2 inclusive
  • Nonsmoker
  • Healthy men between 18 and 55 years, inclusive (Cohorts A and B)
  • Healthy women between 18 and 58 years, inclusive (Cohort C)
  • Healthy men and women between 65 and 85 years of age, inclusive (Cohort D)
  • Men who are sexually active with a woman of childbearing potential and have not had a vasectomy must agree to use a barrier method of birth control during the study and for 3 months after receiving the last dose of study drug. In addition, their female partners should also use an appropriate method of birth control for at least the same duration (Cohorts A, B, and D)
  • Not be of childbearing potential due to either tubal ligation or hysterectomy, or who are postmenopausal (Cohorts C and D)

Exclusion Criteria

  • Clinically significant abnormal values for hematology, clinical chemistry or urinalysis at screening or admission
  • Clinically significant abnormal physical examination, vital signs or electrocardiogram at screening or admission
  • History of, or current, significant medical illness including (but not limited to) cardiac disease, hematological disease, lipid abnormalities, respiratory disease, diabetes mellitus, renal or hepatic insufficiency, thyroid disease, Parkinson's disease, infection, or any other illness that the Investigator considers should exclude the participant
  • History of epilepsy or fits or unexplained black-outs
  • Cohorts A and B only: a contraindication for spinal puncture

Arms & Interventions

Cohort A (Part 1)

Healthy male participants, 18 to 55 years of age.

Intervention: JNJ-42165279 50 mg

Cohort A (Part 1)

Healthy male participants, 18 to 55 years of age.

Intervention: Placebo

Cohort B (Part 1)

Healthy male participants, 18 to 55 years of age.

Intervention: JNJ-42165279 30 mg

Cohort B (Part 1)

Healthy male participants, 18 to 55 years of age.

Intervention: Placebo

Cohort C (Part 2)

Healthy female participants of nonchildbearing potential (surgically sterile or postmenopausal), 18 to 58 years of age.

Intervention: JNJ-42165279 100 mg

Cohort C (Part 2)

Healthy female participants of nonchildbearing potential (surgically sterile or postmenopausal), 18 to 58 years of age.

Intervention: Placebo

Cohort D (Part 2)

Healthy elderly male or female participants, from 65 to 85 years of age.

Intervention: JNJ-42165279 100 mg

Cohort D (Part 2)

Healthy elderly male or female participants, from 65 to 85 years of age.

Intervention: Placebo

Outcomes

Primary Outcomes

Concentrations in cerebrospinal fluid of JNJ-42165279

Time Frame: 2 weeks

Plasma concentrations of JNJ-42165279

Time Frame: 2 weeks

Urine concentrations of JNJ-42165279

Time Frame: 2 weeks

The number of participants with adserve events as a measure of safety and tolerability

Time Frame: Approximately 8 weeks

Secondary Outcomes

  • Enzyme fatty acid amide hydrolase inhibition, as measured in white blood cells (WBCs)(Approximately 4 weeks)
  • Plasma concentrations of N-arachidonoylethanolamine (anandamide)(2 weeks)
  • Plasma concentrations of palmitoylethanolamide(2 weeks)
  • Plasma concentrations of oleoylethanolamide(2 weeks)
  • Serum concentrations of prolactin(10 days)
  • Saliva concentrations of cortisol(10 days)
  • Concentrations in cerebrospinal fluid of N-arachidonoylethanolamine (anandamide) or its metabolites(9 days)
  • Concentrations in cerebrospinal fluid of palmitoylethanolamide or its metabolites(9 days)
  • Concentrations in cerebrospinal fluid of oleoylethanolamide or its metabolites(9 days)

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