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Completed Phase 2 Interventional

A Study of Genetically Targeted Enzyme Replacement Therapy for Advanced Heart Failure

ClinicalTrials.gov ID: NCT01643330

Public ClinicalTrials.gov record NCT01643330. 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, 11:21 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 Phase 2b, Double-Blind, Placebo-Controlled, Multinational, Multicenter, Randomized Study Evaluating the Safety and Efficacy of Intracoronary Administration of MYDICAR® (AAV1/SERCA2a) in Subjects With Heart Failure

Study identification

NCT ID
NCT01643330
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celladon Corporation
Industry
Enrollment
250 participants

Conditions and interventions

Interventions

  • AAV1/SERCA2a (MYDICAR) Genetic
  • Placebo Genetic

Genetic

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Jan 31, 2015
Completion
Jan 31, 2016
Last update posted
Mar 23, 2016

2012 – 2016

United States locations

U.S. sites
29
U.S. states
21
U.S. cities
29
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed La Jolla California
Not listed Long Beach California
Not listed San Diego California
Not listed Sylmar California
Not listed Newark Delaware
Not listed Jacksonville Florida
Not listed Miami Florida
Not listed Augusta Georgia
Not listed Iowa City Iowa
Not listed Alexandria Louisiana
Not listed Boston Massachusetts
Not listed Kansas City Missouri
Not listed St Louis Missouri
Not listed New York New York
Not listed The Bronx New York
Not listed Winston-Salem North Carolina
Not listed Columbus Ohio
Not listed Oklahoma City Oklahoma
Not listed Philadelphia Pennsylvania
Not listed Charleston South Carolina
Not listed Rapid City South Dakota
Not listed Germantown Tennessee
Not listed Tullahoma Tennessee
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Salt Lake City Utah
Not listed Tacoma Washington
Not listed Waukesha 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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01643330, 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 23, 2016 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01643330 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →