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Clinical Trials/NL-OMON30044
NL-OMON30044
Completed
Not Applicable

A Randomized, Double-Blind, Placebo-Controlled Study in Healthy Male Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Oral Doses of JNJ-26070109 - N/A

Janssen-Cilag0 sites82 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
abdominal pain and heartburn
Sponsor
Janssen-Cilag
Enrollment
82
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Healthy males without evidence of gastro\-intestinal disorders

Exclusion Criteria

  • Subjects with evidence of clinically significant reproductive, gastrointestinal, renal, hematologic, pulmonary, neurologic, respiratory, endocrine/metabolic, or cardiovascular system abnormalities, psychiatric disorders, oncologic conditions or acute or chronic infection.
  • Subjects with a history of any hepatic disorder or history of hepatitis.
  • Subjects with known elevations of LFTs, alkaline phosphatase, gamma\-GT, or bilirubin in the past.
  • Negative Helicobacter pylori serum IgG antibody

Outcomes

Primary Outcomes

Not specified

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