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Effect of KW-3902IV in Combination With IV Furosemide on Renal Function in Subjects With CHF and Renal Impairment

Effect of KW-3902IV in Combination With IV Furosemide on Renal Function in Subjects With Congestive Heart Failure (CHF) and Renal Impairment

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00159614
Enrollment
30
Registered
2005-09-12
Start date
2005-09-30
Completion date
Unknown
Last updated
2008-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Congestive, Renal Insufficiency

Keywords

renal insufficiency, diuretic, heart failure, congestive

Brief summary

The purpose of this study is to characterize the safety and tolerability of KW-3902IV and measure its effect on renal function.

Interventions

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
NovaCardia, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Stable congestive heart failure * Impaired renal function * Taking oral loop diuretic

Exclusion criteria

* Acutely decompensated (unstable) and end stage heart failure * Diuretics other than loop diuretics * Pregnant or nursing * Inability to follow instructions * Participation in another clinical trial within past 30 days

Design outcomes

Primary

MeasureTime frame
Comparison of KW-3902IV alone or with loop diuretic on renal function.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026