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Clinical Trials/NL-OMON37911
NL-OMON37911CompletedNot Applicable

PHARMACOKINETICS AND METABOLISM OF 14C-LABELED GRC 4039 SODIUM FOLLOWING A SINGLE ORAL ADMINISTRATION IN HEALTHY MALE VOLUNTEERS - 14C-LABELED GRC 4039 SODIUM STUDY

Glenmark Pharmaceuticals SA0 sites6 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
6

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • healthy male subjects
  • 18-55 yrs, inclusive
  • BMI: 18.5-29.5 kg/m2, inclusive
  • Weight: 55-95 kg, inclusive
  • non-smoking

Exclusion Criteria

  • Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 90 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1.5 liters of blood in the 10 months prior the start of this study.

Investigators

Sponsor
Glenmark Pharmaceuticals SA

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