Status:

COMPLETED

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42721458 in Healthy Male Participants

Lead Sponsor:

Janssen Research & Development, LLC

Conditions:

Healthy

Eligibility:

MALE

18-55 years

Phase:

PHASE1

Brief Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (what the body does to the medication), potential immunogenicity (ability to induce an immune response), and pharmac...

Detailed Description

This is a randomized (the study medication is assigned by chance), double-blind (neither physician nor participant knows the identity of the assigned treatment), placebo-controlled (an inactive substa...

Eligibility Criteria

Inclusion

  • Body mass index (weight kg/m2) between 18 and 30 kg/m2, and body weight not less than 50 kg
  • Participant is judged to be generally in good health based on medical history, physical examination, vital signs and laboratory safety tests
  • Blood pressure between 90 and 135 mmHg systolic, inclusive, and no higher than 90 mmHg diastolic
  • A 12-lead electrocardiogram consistent with normal cardiac conduction and function

Exclusion

  • History of or current clinically significant medical illness
  • Clinically significant abnormal values for hematology, clinical chemistry or urinalysis at screening or on Day -1 (at admission to the study center)
  • Estimated creatinine clearance of less than or equal to 80 mL/min
  • Clinically significant abnormal physical examination, vital signs or 12 lead electrocardiogram at screening or on Day -1
  • Participant demonstrates orthostatic change in vital signs measurements on screening or predose while going from a semi recumbent to standing position
  • History of significant multiple and/or severe allergies (including latex allergies) or known history of clinically significant allergies to polyethylene glycol (PEG) containing or other PEGylated products

Key Trial Info

Start Date :

April 1 2013

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2014

Estimated Enrollment :

108 Patients enrolled

Trial Details

Trial ID

NCT01840501

Start Date

April 1 2013

End Date

April 1 2014

Last Update

May 6 2014

Active Locations (1)

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1

Merksem, Belgium