To Assess the Pharmacokinetics and Safety of Single Doses of JNJ-54452840 in Healthy Japanese and Caucasian Participants

NCT ID: NCT01809353

Last Updated: 2015-03-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-07-31
• Study Completion Date: 2014-09-30

Brief Summary

The purpose of this study is to assess the pharmacokinetics (ie, how the body affects the drug) and safety of JNJ-54452840 in healthy participants.

Detailed Description

This is a Phase 1, randomized (the study treatment is assigned by chance), double-blind (neither physician nor participant knows the treatment received), placebo-controlled (one of the study treatments is inactive), four-way cross-over study (method used to switch participants from one treatment arm to another in a clinical trial) conducted in healthy male Japanese and Caucasian participants. The study will be conducted in 3 parts; a screening phase (up to 28 days), a double-blind treatment phase (28 days), and a follow-up phase (approximately 21 to 28 days). The study will be conducted in 2 groups (Group A consists of 16 Japanese participants; Group B consists of 16 Caucasian participants) over 4 treatment periods. On Day 1 of Period 1, approximately 16 eligible Japanese participants and the same number of eligible Caucasian participants will be randomly assigned to 1 of 4 treatment sequences and will receive the 4 intravenous treatments JNJ-54452840 20 mg, JNJ-54452840 80 mg, JNJ-54452840 240 mg, and placebo across the treatment periods according to the order specified by the randomization schedule.

Participants will come to the study center each time they receive study medication and will be discharged from the study center 24 hours after dosing during each treatment period after satisfactory review of all clinical safety measures. Blood samples will be drawn at time points during the treatment and follow-up periods for participants in both Group A and Group B of the study. Participants will return to the study center for a follow-up visit within approximately 7 to 10 days after the last study procedure in the last treatment period for safety assessments, followed by another visit within approximately 21 to 28 days for assessment of anti -beta-1-AR (adrenergic receptor) auto-antibodies in blood (auto-antibodies targeting the human beta-1-AR antibody). If anti-beta-1-AR auto-antibodies are detected at this second follow-up visit, additional testing will be performed every 3 months until autoantibody levels fall below the level of detection of the assay or for 1 year, whichever occurs earlier. Participants in Group A and Group B will be involved in the study for approximately 12 weeks and up to 1 year if they develop anti -beta-1-AR auto-antibodies . Safety of the participants will be monitored throughout the study.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Group A: JNJ-54452840 20 mg

Each participant will receive 20 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group A: JNJ-54452840 80 mg

Each participant will receive 80 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group A: JNJ-54452840 240 mg

Each participant will receive 240 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group A: Placebo

Each participant will receive matching placebo as a single intravenous dose.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Single matching intravenous dose

Group B: JNJ-54452840 20 mg

Each participant will receive 20 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group B: JNJ-54452840 80 mg

Each participant will receive 80 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group B: JNJ-54452840 240 mg

Each participant will receive 240 mg of JNJ-54452840 as a single intravenous dose.

Group Type: EXPERIMENTAL

JNJ-54452840

Intervention Type: DRUG

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Group B: Placebo

Each participant will receive matching placebo as a single intravenous dose.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Single matching intravenous dose

Interventions

JNJ-54452840

Single intravenous (medication is injected into a vein) doses of 20 mg, 80 mg, and 240 mg

Intervention Type: DRUG

Placebo

Single matching intravenous dose

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Must be a healthy male with no clinically relevant abnormalities as determined by medical history, physical examination, blood chemistry assessments, hematologic assessments - Must be Japanese or Caucasian
• Japanese participants must have been born in Japan, have resided outside of Japan for no more than 5 years, and have Japanese parents and maternal and paternal grandparents
• Caucasian participants must have Caucasian parents

Exclusion Criteria

• History of or current clinically significant medical illness that the investigator considers should exclude the participant or that could interfere with the interpretation of the study results
• Have a known or suspected intolerance or hypersensitivity to any biologic medication or known allergies or clinically significant reactions to murine, chimeric, or human peptides or protein
• Be unable or unwilling to undergo multiple venipunctures because of poor tolerability or lack of easy access to veins

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Janssen Research & Development, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Janssen Research & Development, LLC Clinical Trial

Role: STUDY_DIRECTOR

Janssen Research & Development, LLC

Locations

Cypress, California, United States

Countries

United States

Related Links

http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=3650&filename=CR100982_CSR.pdf

A Phase 1 Randomized, Double-Blind, Placebo-Controlled Crossover Study to Evaluate the Pharmacokinetics and Safety of JNJ-54452840 Following Single Intravenous Doses to Healthy Male Japanese and Caucasian Subjects

Other Identifiers

54452840HFA1001

Identifier Type: OTHER

Identifier Source: secondary_id

CR100982

Identifier Type: -

Identifier Source: org_study_id