Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Avid Radiopharmaceuticals
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Subjects who have a historical volumetric magnetic resonance imaging (MRI) as part of the companion study
You may not be if
Have clinically significant cardiac, hepatic, renal, pulmonary, metabolic, or endocrine disturbances
Have a screening electrocardiogram with a corrected QT interval (QTc) \> 450 msec if male or QTc \> 470 msec if female
Have a history of additional risk factors for Torsades de Pointes (TdP) or are taking drugs known to cause QT-prolongation. Patients with a prolonged QTc interval in the setting of intraventricular conduction block may be enrolled with sponsor approval
Have a history of drug or alcohol dependence within the last year, or prior prolonged history of dependence unless approved by the sponsor
Are females of childbearing potential who are not surgically sterile, not refraining from sexual activity or not using reliable methods of contraception
Have a history of relevant severe drug allergy or hypersensitivity
Are patients who have received an investigational medication within 30 days prior to the planned imaging session for this study
Are patients with current clinically significant unstable medical comorbidities
Are patients who have received a radiopharmaceutical for imaging or therapy within the past 24 hours prior to the imaging session for this study