RAdiolabeled Perfusion to Identify Coronary Artery Disease Using WAter To Evaluate Responses of Myocardial FLOW (RAPID-WATER-FLOW)

Running, not enrolling · Phase 3

Conditions studied: Coronary Artery Disease

In brief

This a Phase 3, prospective, open-label, multicenter study of \[15-O\]-H2O injection for PET imaging of subjects with suspected CAD. Approximately 182 evaluable participants with suspected CAD referred for testing will be included in the study at approximately 10 study sites in the United States and Europe. Approximately 215 participants will be enrolled to account for an estimated 15% drop-out rate. Screening assessments will occur prior to enrollment to confirm eligibility. All participants will receive two doses of \[15-O\]-H2O as part of a single PET imaging session (one dose at rest and one during pharmacological stress with adenosine). A safety follow-up phone call will occur 24 ± 8 hrs after completion of the \[15-O\]-H2O scan.

Key facts

Study ID

NCT05134012

Run by

MedTrace Pharma A/S

People needed

215

Starts

2022-05-08

Expected to finish

2026-10-01

Last updated by the study team

2026-07-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female participants ≥18 years;
• Informed consent form (ICF) read, signed, and dated prior to any study procedures being performed;
• Participants who fall into any one of the following categories:
• Have been referred for an ICA directly of after non-invasive testing (e.g., SPECT or PET MPI, stress echo, CCTA, ETT).
• Had an ICA with no intervention. However, if any stenosis >40% but ≤70% was observed, an FFR or iFR assessment was performed.
• Had a CCTA with normal coronaries or minimal CAD (no stenosis >25%).
• The SPECT study, PET 15O-H2O study, and ICA or CCTA testing need to be completed within a 30-day window, with time 0 defined as the date of the first of these three tests.
• Women of Child Bearing Potential (WOCBP) must be non-pregnant, and non-lactating. For women of childbearing potential, the results of a urine human chorionic gonadotropin (HCG) pregnancy test (with the result known on the day of drug administration) must be negative; these participants must be practicing appropriate birth control from time of the screening visit until the end of the follow-up period. For women who are either surgically sterile (have a documented bilateral tubal ligation or oophorectomy and/or hysterectomy) or are post-menopausal (cessation of menses for more than 1 year), enrollment in the study without a pregnancy test at screening is allowed.
• Male will need to use contraceptive methods until end of the follow-up period.
• Participants are able to comply with all study procedures as described in the protocol.

You may not qualify if…

• Participants are unable to undergo (even partially) any of the imaging procedures;
• Participants with a known history of cardiac disease including:
• myocardial infarction, previous coronary revascularization, or chronic ischemic cardiomyopathy
• primary myocardial disease such as cardiac amyloidosis or hypertrophic cardiomyopathy
• known left ventricular dysfunction
• moderate or severe aortic or mitral stenosis or regurgitation
• Participants in whom adenosine stress testing is contraindicated, including but not limited to:
• Participants with severe COPD or chronic asthma.
• Participants with second- or third-degree atrioventricular block without a pacemaker.
• Participants with claustrophobia to an extent that would limit their ability to undergo SPECT and PET imaging (patients whose claustrophobia is known to be readily controlled with drugs or psychological support may be enrolled).
• Participants who are on sildenafil (Viagra) or oral dipyridamole (Persantine, Aggrenox) therapy or on any PDE5 inhibitor (i.e. tadalafil, avanafil, vardenafil),and for whom its use cannot be terminated or suspended for ≥24 hours prior to treatment of study drug.
• Participants with significant co-morbidities that would prevent appropriate completion of the protocol procedures.
• Participants who have participated in another research study using investigational drugs within the 30 days prior to enrollment or through the duration of the trial (patients in observational studies with approved agents and participants known to be on placebo may be enrolled).
• Participants who have previously participated in this study.
• Subjects scheduled for, or planning to undergo, any interventional cardiac procedures between enrollment and ICA (pathway 1) or signing of informed consent and 15O-H2O PET MPI (pathway 2 and 3)

Where it is running

• University of Iowa — Iowa City, Iowa, United States
• Mayo Clinic — Rochester, Minnesota, United States
• Washington University — St Louis, Missouri, United States
• University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
• UT Southwestern Medical Center — Dallas, Texas, United States
• University of Virginia Medical Center — Charlottesville, Virginia, United States
• University of Ottawa Heart Institute — Ottawa, Ontario, Canada
• Aarhus University Hospital — Aarhus, Denmark
• University Hospital Freiburg, Clinic for Nuclear Medicine — Freiburg im Breisgau, Germany
• Department of Cardiology and Angiology -- Hannover Medical School (MHH) — Hanover, Germany
• Amsterdam University Medical Center, Department of Radiology and Nuclear Medicine — Amsterdam, North Holland, Netherlands
• Sahlgrenska University Hospital — Gothenburg, Sweden
• Norrland University Hospital Heart Center — Umeå, Sweden

Full record on ClinicalTrials.gov

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