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Completed Phase 3 Interventional Results available

Efficacy and Safety of Targeted Intramyocardial Delivery of Auto CD34+ Stem Cells for Improving Exercise Capacity in Subjects With Refractory Angina

ClinicalTrials.gov ID: NCT01508910

Public ClinicalTrials.gov record NCT01508910. 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 Oct 22, 2026, 7:31 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 Prospective, Randomized, Double-blinded, Active-control and Unblinded Standard of Care (SOC) Controlled Study to Determine the Efficacy and Safety of Targeted Intramyocardial Delivery of Autologous CD34+ Cells (Auto-CD34+ Cells) for Increasing Exercise Capacity During Standardized Exercise Testing in Subjects With Refractory Angina Pectoris and Chronic Myocardial Ischemia

Brief summary

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

The purpose of the study is to assess the safety and efficacy of targeted intramyocardial delivery of Auto-CD34+ cells for increasing exercise time and amelioration of anginal symptoms in subjects with refractory angina and chronic myocardial ischemia.

Study identification

NCT ID
NCT01508910
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Lisata Therapeutics, Inc.
Industry
Enrollment
291 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 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
Apr 2012 (Type not available)
Primary completion
Nov 2015 (Actual)
Completion
Nov 2015 (Actual)
Last update posted
Dec 19, 2018

2012 – 2015

United States locations

U.S. sites
41
U.S. states
22
U.S. cities
41
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Gilbert Arizona — —
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Not listed La Jolla California — —
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Not listed Atlanta Georgia — —
Not listed Augusta Georgia — —
Not listed Chicago Illinois — —
Not listed Iowa City Iowa — —
Not listed Louisville Kentucky — —
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Not listed Boston Massachusetts — —
Not listed Saginaw Michigan — —
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Not listed Rochester Minnesota — —
Not listed Haddon Heights New Jersey — —
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Not listed Pittsburgh Pennsylvania — —
Not listed Germantown Tennessee — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Salt Lake City Utah — —
Not listed Seattle Washington — —
Not listed Madison Wisconsin — —
Not listed 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01508910, 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 Dec 19, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01508910 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →