Altropane Dose for Imaging Patients With Suspected Parkinson's Disease

Inclusion Criteria:

• For Part 1: a) the participant had a DaTscan image, obtained within 1 year (preferably within 6 months) before screening, that showed normal striatal uptakeand b) the participant had a clinical diagnosis (made by a board-certifiedneurologist who was qualified by training and experience in the diagnosis ofmovement disorders) that was consistent with the DaTscan image.

For Part 2 (which was not conducted): a) the participant had a DaTscan image, obtained within 1 year (preferably within 6 months) before screening, that showed abnormal (unilateral or bilateral reduced) striatal uptake and b) the participant also had a confirmed clinical diagnosis of a dPS (such as Parkinson's disease, multiple system atrophy, corticobasal degeneration, progressive supranuclear palsy, etc.) made by a board-certified neurologist who was qualified by training and experience in the diagnosis of movement disorders, and c) the diagnosis was consistent with the DaTscan image.

• The participant was male or female, ≥18 years of age, of any race and ethnicity.

• The participant was able and willing to comply with study procedures and signed anddated informed consent was obtained.

• If the participant was a woman of childbearing potential*, she must have used ahighly effective method of contraception** from Screening until 30 days after thelast administration of Altropane, and the results of a serum or urine humanchorionic gonadotropin (hCG) pregnancy test, performed at Screening and on the dayof Altropane administration (with the result known before Altropane administration),must have been negative.

• A woman of childbearing potential was defined as neither post-menopausal norsurgically sterile. Post-menopausal means having had no menses for at least 12months without an alternative medical cause. Surgically sterile means having had adocumented hysterectomy, bilateral salpingectomy, or bilateral oophorectomy, or anycombination of these.

** A highly effective method of contraception was defined as one that had a failurerate of less than 1% per year when used consistently and correctly; such methodsincluded combined (estrogen and progestogen containing) hormonal contraceptionassociated with inhibition of ovulation (oral, intravaginal, or transdermal);progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, or implantable); intrauterine device; intrauterinehormone-releasing system; bilateral tubal ligation/occlusion; vasectomized partner (with medical confirmation of success); and abstinence from heterosexual intercourseinvolving a woman of childbearing potential.

• If the participant was a male*** with a sexual partner who was a woman ofchildbearing potential*, he and his partner must have used adequate contraception**from Screening until 30 days after the last administration of Altropane.

(***A male was considered fertile after puberty unless permanently sterile by bilateral orchidectomy, or vasectomized with confirmation of success.)

Exclusion Criteria:

• The participant was previously included in this study.

• Fewer than 7 disintegration half-lives had elapsed between the participant's lastprocedure (therapeutic or diagnostic) involving a radioisotope and Visit 2 (altropane SPECT imaging).

• Including participation in this study, the participant's total exposure to radiationduring medical procedures/tests in the past year would have exceeded 50 mSv.

• The participant had participated in an investigational drug or device clinical trialwithin 30 days before the date of informed consent.

• The participant had any clinically significant or unstable physical or psychologicalillness, structural brain abnormality, abnormal laboratory results, or abnormal ECG (based on medical history or physical examination at Screening), as determined bythe Principal Investigator, that would interfere with study participation.

• The participant had any history of drug or alcohol abuse in the 2 years prior to thedate of informed consent.

• The participant had a positive urine screen for drugs of abuse at Screening.

• The participant was a pregnant or breast-feeding female, or was a female ofchild-bearing potential that was not using appropriate birth control.

• The participant was unable to lie supine for 1 hour.

• The participant had any thyroid disease other than adequately treatedhypothyroidism.

• The participant had known or suspected allergy/hypersensitivity to any ingredient inAltropane or to the thyroid blocking medication to be used before imaging.

• The participant was taking any of the medications/treatments listed in the protocolas disallowed and could not or would not discontinue use at least 12 hours prior toSPECT exam.

• The participant was referred to DaTscan imaging for evaluation of possible cognitiveimpairment including dementia.