A single center, phase 0/1 clinical imaging study designed to assess the role of \[68Ga\]Galmydar PET/CT imaging in human subjects.
Who can participate
Age range18 Years – 99 Years
SexALL
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Inclusion Criteria:
* Male and female, 18-99 years of age and any race;
* Have had a prior clinical SPECT or PET MPI positive for ischemia in two myocardial segments and referred for invasive coronary angiography (ICA) or have had a prior clinical SPECT or PET MPI negative for ischemia or healthy adult normal volunteers who are asymptomatic, without history of cardiovascular disease or significant cardiovascular risk factors;
Exclusion Criteria:
* Inability to receive and sign informed consent;
* Percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) within 6-months prior to clinical SPECT or PET or in the intervening days between clinical SPECT or PET and research PET examination;
* Participants who have received chemotherapeutic agents within 6 months of enrollment;
* Heart failure (left ventricular ejection fraction ≤ 20%);
* Known non-ischemic cardiomyopathy;
* Inability to undergo pharmacologic stress testing with regadenoson (Lexiscan). Contraindications include:
* Symptomatic bradycardia or second to third degree atrioventricular (AV) block;
* Pre-existing obstructive lung disease with active wheezing, i.e., COPD, asthma with active wheezing that precludes the safe administration of the pharmacological stress agent according to the approved label;
* Uncontrolled and severe hypertension (e.g. systolic blood pressure \>200 mmHg, diastolic blood pressure \>110 mmHg);
* Baseline hypotension (e.g. systolic blood pressure \< 90 mmHg, d…
What they're measuring
1
Semiquantitative assessment of 68Ga-Galmydar PET/CT uptake
Timeframe: Up to 120 minutes post-injection of 68Ga-Galmydar