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Completed Phase 2 Interventional

PROCLAIM: Effect of AC2592 Administered by Continuous Subcutaneous Infusion in Subjects With Advanced Chronic Congestive Heart Failure

ClinicalTrials.gov ID: NCT00099580

Public ClinicalTrials.gov record NCT00099580. 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 Jun 26, 2026, 2:04 AM EDT

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

Official title

PROCLAIM: A Phase 2, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multicenter Study to Examine the Effects of AC2592 Administered by Continuous Subcutaneous Infusion in Subjects With Advanced Chronic Congestive Heart Failure

Study identification

NCT ID
NCT00099580
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
61 participants

Conditions and interventions

Interventions

  • AC2592 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
Feb 28, 2005
Primary completion
Aug 31, 2006
Completion
Aug 31, 2006
Last update posted
Jan 18, 2015

2005 – 2006

United States locations

U.S. sites
29
U.S. states
19
U.S. cities
29
Facility City State ZIP Site status
Research Site Beverly Hills California
Research Site Mission Viejo California
Research Site New Haven Connecticut
Research Site Washington D.C. District of Columbia
Research Site Jacksonville Florida
Research Site Tampa Florida
Research Site Peoria Illinois
Research Site Springfield Illinois
Research Site Winfield Illinois
Research Site Wichita Kansas
Research Site Baton Rouge Louisiana
Research Site Shreveport Louisiana
Research Site Auburn Maine
Research Site Boston Massachusetts
Research Site Detroit Michigan
Research Site Lincoln Nebraska
Research Site Chapel Hill North Carolina
Research Site Durham North Carolina
Research Site Cincinnati Ohio
Research Site Cleveland Ohio
Research Site Columbus Ohio
Research Site Oklahoma City Oklahoma
Research Site Medford Oregon
Research Site Portland Oregon
Research Site Philadelphia Pennsylvania
Research Site Charleston South Carolina
Research Site Knoxville Tennessee
Research Site Dallas Texas
Research Site Houston Texas

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00099580, 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 Jan 18, 2015 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00099580 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →