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Efficacy of EVP 1001-1 (SeeMore) in the Assessment of Myocardial Viability in Patients With Cardiovascular Disease
Not Recruiting
Trial ID: NCT01989195
Purpose
The investigator hopes to introduce a novel MRI contrast agent with SeeMore ™ that directly
defines viable myocardium. Identifying viable myocardium non-invasively using cardiac MRI is
still a moving target and a question we plan to answer more definitively with the SeeMore ™
contrast. Though well tested in small and large animals and Phase I & II clinical trials, the
investigators would like to determine the efficacy of the SeeMore contrast further in a
clinical setting.
SeeMore is a new manganese (Mn)-based intravenous imaging agent being developed to enhance
magnetic resonance imaging (MRI). While Mn has long been known to have desirable magnetic and
kinetic properties for MRI, use in humans was not initially possible due to cardiovascular
depression and electrocardiogram (ECG) changes, including prolongation of PR and QTc
intervals, associated with intravenous administration [1-5]. SeeMore provides Mn in a form
that maintains the desired magnetic and kinetic properties while overcoming the
cardiovascular toxicity of Mn. SeeMore is taken up into heart cells (primarily via addition
of calcium to avoid cardiotoxic effects; please refer to US patent #5,980,863). The potential
to distinguish healthy heart tissue from unhealthy heart tissue based on a specific sustained
pattern of enhancement provides a basis for evaluating the performance of SeeMore in heart
patients. It may be possible to enhance the utility of MRI for heart disease through the use
of an imaging agent that is specifically taken up into heart cells. SeeMore is the only
cardiac-specific agent being developed for this purpose. Unlike nuclear perfusion agents,
SeeMore is not radioactive and does not require special handling, shielding, transport or
storage. In addition, the specific pattern of enhancement achieved in the heart muscle
persists over time, offering potential benefits over the nonspecific extracellular agents
currently available for MRI or X-ray/CT procedures. This feature allows full use of the high
resolution of MRI, since there is not a trade-off of high spatial resolution for temporal
(first-pass) resolution. It is anticipated the features offered by SeeMore along with the
high resolution, three dimensional attributes of MRI will result in higher accuracy than is
available with other current modalities in practice, including stress echocardiograms,
cardiac MRI using gadolinium contrast and nuclear studies such as SPECT and PET. This will be
evaluated in this study and serve as the basis for pivotal registration studies.
All components of SeeMore™ are USP and are approved for use as drugs in man, orally and/or
intravenously.
Official Title
Efficacy of EVP 1001-1 (SeeMore) in the Assessment of Myocardial Viability in Patients With Cardiovascular Disease
Stanford Investigator(s)
Phillip C. Yang, MD
Professor of Medicine (Cardiovascular Medicine)
Eligibility
Inclusion Criteria:
-
All subjects to be entered must:
- be at least 18 years of age.
- if female, be nonpregnant as evidenced by a serum pregnancy test and using a
medically-approved method of birth control, or post-menopausal or surgically sterile
- provide written informed consent after having received oral and written information
about the study
- be in stable health based on medical history, examination and tests
Exclusion Criteria:
- have a positive pregnancy test (females)
- received an investigational drug or device within 30 days prior to administration of
SeeMore?
- have known hypersensitivity to ondansetron or other selective serotonin 5HT3 receptor
blockers
- have a history of drug abuse or alcoholism
- are taking a digitalis preparation or calcium channel blocker
- have a history of torsades or prolonged QT/QTc interval
- have NYHA Grade IV heart failure
- have abnormal liver function tests or a history of liver disease
- have uncontrolled hypertension (Systolic Blood Pressure > 140 or Diastolic BP > 90
consistently at baseline)
- have abnormal baseline potassium or calcium values or hemoglobin less than 10 g/dl
- are noncompliant or otherwise unlikely to perform as required by the protocol
- have pretest likelihood of CAD for which the requisite number of subjects have been
entered
- develop an arrhythmia prior to or during either of the exercise tests; SeeMore? should
not be administered.
Intervention(s):
drug: 'SEEMORE' - MANGANESE-ENHANCED MRI CONTRAST REAGENT
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305