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Evaluation of CCR2 in Patients Post Myocardial Infarction

Preliminary Evaluation of 64Cu-DOTA-ECL1i in Patients Post-ST-Elevation Myocardial Infarction(STEMI)

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05107596
Enrollment
90
Registered
2021-11-04
Start date
2018-11-24
Completion date
2025-11-24
Last updated
2022-11-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Diseases

Brief summary

To determine the feasibility of 64Cu-DOTA-ECL1i, an investigational PET imaging drug, at the cellular level in the myocardium for individuals who have suffered a heart attack or who have other inflammatory heart disease.

Detailed description

To determine the feasibility of 64Cu-DOTA-ECL1i to detect CCR2+monocytes and macrophages which are cells that are responsible for protecting tissues from foreign substances in the myocardium by PET/MR and PET/CT.

Interventions

Inject PET Radioisotope for imaging

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Healthy Volunteers: 2. Age 21 to 80 years of either sex, any race 3. Capable of lying still and supine within the PET/CT and PET/MR scanner for 1 hour and follow instructions for breathing protocol during the CT portion 4. No illicit drug use or other inhaled drug use (including pharmacologic agents, recreational agents, or illicit drugs) within the past year 5. No known history of cardiac. pulmonary, hepatic, or renal disease or diabetes 6. No history of claustrophobia or other preventing condition that has previously or would interfere with completion of protocol-specified imaging sessions 7. Able to comprehend and willing to follow instructions for the study procedures as called for by the protocol. Inflammatory Heart Disease 1. Age 21 to 80 years of either sex, any race who have suffered a STEMI within the past 6 months as well as other forms of inflammatory heart disease including sarcoidosis, myocarditis, cardiomyopathy, injected cardiovascular implantable electronic devices pacemakers/LVAD 2. Are clinically stable to undergo imaging with either PET/MR or PET/CT. 3. Capacity to give written informed consent and ability to follow study procedures 4. Pre-menopausal women must have a negative urine pregnancy test within 24 hours prior to the administration of 64-Cu-DOTA-ECL1i.

Exclusion criteria

Healthy volunteers: 1. Currently enrolled in another study using an investigational drug 2. Angina 3. Uncontrolled heart failure 4. uncontrolled hypertension baseline hypotension below 90/50 5. Has any condition that in the opinion of the PI or designee that could increase risk to the subject 6. Is deemed likely to be unable to perform all research procedures 7. Have contraindications to PET/CT imaging like claustrophobia 8. Have contraindication to gadolinium 9. Pregnant or breastfeeding 10. Currently using recreational drubs 11. Body weight of more than 300 lbs 12. Active symptoms or history of cardiac, pulmonary, hepatic or renal disease or diabetes 13. currently taking any prescription medications 14. Presence of an implanted device incompatible with CT or MRI scanning Inflammatory Heart Disease 1\) Clinically unstable including post MI angina, uncontrolled heart failure, sever hypertension, hypotension AV block 2) Has any condition that in the opinion of the PI could increase risk to the subject 3) Claustrophobia 4) contraindication to gadolinium contrast 5) Pregnant 6) Currently using recreational drugs 7) Body Weight more than 300 lbs 8) Currently enrolled in another study

Design outcomes

Primary

MeasureTime frameDescription
Number of participants who have heart disease as shown in the images1 or 2 daysPET images will be reconstruction using an iterative algorithm that incorporates resolution recovery, and will be corrected for attenuation using their respective CT or MR data sets

Countries

United States

Contacts

Primary ContactKitty D Harrison, BSN, RN
kittydharrison@wustl.edu314-747-0183

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026