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Terminated Phase 2 Interventional

Safety and Efficacy Study to Evaluate the Effect of SLV320 on Renal Function in Patients With Worsening Heart Failure

ClinicalTrials.gov ID: NCT00744341

Public ClinicalTrials.gov record NCT00744341. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Placebo-Controlled, Randomized, Multi-Center, Dose-Finding Study of SLV320, a Selective A1 Adenosine Receptor Antagonist, to Evaluate the Effect on Renal Function and Safety in Subjects Hospitalized With Acute Decompensated Heart Failure and Renal Dysfunction (Reno-Defend 1)

Study identification

NCT ID
NCT00744341
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
46 participants

Conditions and interventions

Interventions

  • SLV320 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2009
Primary completion
Dec 31, 2009
Completion
Dec 31, 2009
Last update posted
Sep 16, 2010

2009 – 2010

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
27
Facility City State ZIP Site status
S320.2.011 Site # 548 Alameda California
S320.2.011 Site # 566 Banning California
S320.2.011 Site # 551 Inglewood California
S320.2.011 Site # 564 Bridgeport Connecticut
S320.2.011 Site # 505 Hollywood Florida
S320.2.011 Site # 507 Jacksonville Florida
S320.2.011 Site # 532 Riverdale Georgia
S320.2.011 Site # 513 Chicago Illinois
S320.2.011 Site # 561 Indianapolis Indiana
S320.2.011 Site # 526 Owensboro Kentucky
S320.2.011 Site # 504 Natchitoches Louisiana
S320.2.011 Site # 546 Biddeford Maine
S320.2.011 Site # 523 Dearborn Michigan
S320.2.011 Site # 534 Detroit Michigan
S320.2.011 Site # 558 Detroit Michigan
S320.2.011 Site # 508 St Louis Missouri
S320.2.011 Site # 541 Brooklyn New York
S320.2.011 Site # 537 New York New York
S320.2.011 Site # 521 Akron Ohio
S320.2.011 Site # 527 Toledo Ohio
S320.2.011 Site # 528 Philadelphia Pennsylvania
S320.2.011 Site # 510 Colombia South Carolina
S320.2.011 Site # 545 Nashville Tennessee
S320.2.011 Site # 519 Tullahoma Tennessee
S320.2.011 Site # 511 Houston Texas
S320.2.011 Site # 518 San Antonio Texas
S320.2.011 Site # 556 Manitowoc Wisconsin
S320.2.011 Site # 565 Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 77 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00744341, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 16, 2010 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00744341 live on ClinicalTrials.gov.

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