Overview

PET Study Examining the Dopaminergic Activity of Armodafinil in Adults

Status:
Completed
Trial end date:
2010-05-01
Target enrollment:
0
Participant gender:
All
Summary
The specific aims of this study are 1) to document the Dopamine Transporter (DAT) receptor occupancy of armodafinil using positron emission tomography (PET) scanning with C-11 altropane as the ligand and 2) to document the increased intrasynaptic dopamine produced by armodafinil using PET scanning with C-11 raclopride as the ligand. We hypothesize that DAT occupancy will be low with armodafinil; less than the DAT occupancy produced by therapeutic doses of methylphenidate. We also hypothesize that increases in intrasynaptic dopamine will be relatively low with armodafinil.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Massachusetts General Hospital
Treatments:
Armodafinil
Dopamine
Dopamine Agents
Dopamine Agonists
Modafinil
Criteria
Inclusion Criteria:

1. Signed written informed consent to participate in the study.

2. Age: 18 - 35

3. If female, non-pregnant, non-nursing with a negative serum pregnancy test and using an
adequate form of birth control.

4. Supine and standing blood pressure within the range 110/60 to 150/95 mmHg.

5. Heart rate, after resting for 5 minutes, within the range 46-90 beats/min.

6. Right-handed.

Exclusion Criteria:

1. Diagnosis of any psychotic disorder, bipolar disorder, severe depression, severe
anxiety, or Autism.

Subjects with mild mood, oppositional, conduct, and anxiety disorders may be permitted
to participate if considered appropriate by the investigator.

2. Scores of Baseline Scales:

Hamilton Depression Scale > 17 (out of a possible 67 on the 21-item scale)(Hamilton
1960) Beck Depression Inventory > 19 (out of a possible 63 on the 21-item scale)(Beck,
Ward et al. 1961) Hamilton Anxiety Scale > 21 (out of a possible 56 on the 14-item
scale) (Hamilton 1959)

3. Tics or Tourette's Syndrome.

4. History of head trauma with loss of consciousness, organic brain disorders, seizures,
or neurosurgical intervention.

5. Any clinically significant chronic medical condition, in the judgment of the
investigator.

6. Mental impairment as evidenced by an I.Q. <75.

7. Exposure to dopamine receptor antagonists within the previous three (3) months.

8. Exposure to radiopharmaceuticals within four (4) weeks prior to PET scan.

9. Subjects receiving psychotropic medication.

10. Any clinically significant abnormality in the screening laboratory tests, vital signs,
or 11-lead ECG, outside of normal limits.

11. Any woman of childbearing potential who is seeking to become pregnant or suspects that
she may be pregnant.

12. Subjects with a known recent history (within the past six (6) months) of illicit drug
or alcohol dependence.