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Not listed Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of JVS-100 Administered to Adults With Ischemic Heart Failure.

ClinicalTrials.gov ID: NCT01643590

Public ClinicalTrials.gov record NCT01643590. 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 Sep 12, 2026, 8:28 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 Phase II Randomized, Double-Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of a Single Dose of JVS-100 Administered by Endomyocardial Injection to Cohorts of Adults With Ischemic Heart Failure

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a randomized, double-blind, placebo controlled Phase II study is designed to assess the safety and efficacy of using JVS-100 to treat heart failure.

Study identification

NCT ID
NCT01643590
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Juventas Therapeutics, Inc.
Industry
Enrollment
90 participants

Conditions and interventions

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
Jun 30, 2012
Primary completion
Sep 30, 2014
Completion
Oct 31, 2014
Last update posted
Feb 6, 2014

2012 – 2014

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Cardiology PC Birmingham Alabama 35211
University of Florida Gainesville Florida 32603
Pepin Heart Institute Tampa Florida 33613
Iowa Heart Center Des Moines Iowa 50026
Johns Hopkins University Baltimore Maryland 21287
Spectrum Health Grand Rapids Michigan 49503
Michigan Cardiovascular Institute Saginaw Michigan 48601
Minneapolis Heart Institute Minneapolis Minnesota 55407
Washington University in St. Louis St Louis Missouri 63110
Columbia University Medical Center New York New York 10032
Montefiore Medical Center New York New York 10476
Summa Health System Akron Ohio 44309
The Lindner Center at the Christ Hospital Cincinnati Ohio 45238
University of Pennsylvania Health System Philadelphia Pennsylvania 19104
Baylor Healthcare Dallas Texas 75226
University of Utah Salt Lake City Utah 84132

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 NCT01643590, 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 Feb 6, 2014 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01643590 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →