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Terminated Phase 2 Interventional

Study of DITPA in Patients With Congestive Heart Failure

ClinicalTrials.gov ID: NCT00103519

Public ClinicalTrials.gov record NCT00103519. 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 22, 2026, 4:04 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

A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of DITPA in Patients With NYHA Class III and IV Congestive Heart Failure Who Have Low Serum T3 Levels

Study identification

NCT ID
NCT00103519
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Titan Pharmaceuticals
Industry
Enrollment
86 participants

Conditions and interventions

Interventions

  • DITPA (3,5-diiodothyropropionic acid) 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
Nov 30, 2004
Primary completion
Nov 30, 2006
Completion
Nov 30, 2006
Last update posted
Mar 28, 2013

2004 – 2006

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
The Heart Center Huntsville Alabama 35806
Cardiac Solutions Peoria Arizona 85381
University of Arizona Sarver Heart Center Tucson Arizona 85724
University of Southern California Los Angeles California 90033
UCLA Medical Center Los Angeles California 90095
University of California, San Francisco San Francisco California 94143
Cardiovascular Consultants Medical Group Walnut Creek California 94598
Saint Joseph's Research Institute Atlanta Georgia 30342
Rush University Medical Center Chicago Illinois 60612
University of Louisville Louisville Kentucky 40202
Louisiana State University Health Science Center Shreveport Louisiana 71103
Mayo Clinic Rochester Minnesota 55905
Columbia University New York Presbyterian Hospital New York New York 10032
Cincinnati VA Medical Center Cincinnati Ohio 45220
Clevaland Clinic Foundation Cleveland Ohio 44195
Oklahoma Foundation for Cardiovascular Research Oklahoma City Oklahoma 73120
Oregon Health Sciences University Portland Oregon 97239
Milton S. Hershey Medical Center Hershey Pennsylvania 17033
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213
Baylor University Medical Center Heart Place Dallas Texas 75226
The University of Virginia Health System Charlottesville Virginia 22908
William S. Middleton Memorial Veterans Hospital Madison Wisconsin 53705

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 NCT00103519, 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 Mar 28, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00103519 live on ClinicalTrials.gov.

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