Heart Failure Clinical Trial

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Study to Evaluate TRV120027 on Renal Pharmacodynamics in Patients With Heart Failure and Renal Dysfunction

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Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of TRV120027 in subjects with heart failure and mild to moderate renal dysfunction.

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Eligibility Criteria

Inclusion Criteria:

Written Informed Consent
Heart Failure
Mild to moderate renal dysfunction
Age 18- <75
Males and females (non-childbearing potential)

Exclusion Criteria:

Any significant disease or condition that would interfere with the interpretation of safety or efficacy or efficacy data as determined by the Investigator based on medical history, physical examination or laboratory tests
Any other serious life threatening disease that may impair the interpretation of safety or efficacy data from the study as determined by the Investigator
Allergy or clinically-significant intolerance to ARBs or ACE inhibitors
Clinical signs or symptoms of acute decompensated heart failure
Pregnant or lactating

Study is for people with:

Heart Failure

Phase:

Phase 1

Estimated Enrollment:

17

Study ID:

NCT01444872

Recruitment Status:

Completed

Sponsor:

Trevena Inc.

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There are 4 Locations for this study

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Orlando Clinical Research Center
Orlando Florida, 32809, United States
DaVita Clinical Research
Minneapolis Minnesota, 55404, United States
Duke Clinical Research Unit
Durham North Carolina, 27705, United States
New Orleans Center for Clinical Research
Knoxville Tennessee, 37920, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 1

Estimated Enrollment:

17

Study ID:

NCT01444872

Recruitment Status:

Completed

Sponsor:


Trevena Inc.

How clear is this clinincal trial information?

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