PK/PD Pediatric ADHD Classroom Study

This is a randomized, double-blind, 4-treatment and 4-period crossover study conducted in a
school laboratory environment to evaluate the hour-by-hour behavioral instrument scores and
hour-by-hour PK of 3 different extended-release MPH formulations as well as placebo in
children with ADHD. The complete study consists of three periods: Screening, Dose Titration
and Double-Blind Crossover in a Laboratory Classroom.

The double-blind phase will consist of four periods (or four weeks): each week will consist
of blinded administration with one of the three active methylphenidate hydrochloride
treatments or placebo from Sunday through Saturday. On the last day of each period
(Saturday), study participants will be evaluated in a laboratory classroom setting. On
Saturdays, the blinded doses of each study drug will be administered at the school site by
study staff on the morning of the test laboratory classroom day. On the other days, the
medication will be taken in the morning at home.

Inclusion Criteria:

1. Male and female outpatients

2. Ages 6-12 years at time of screening

3. Judged by the investigator to be physically healthy and suitable for participation in
the study

4. Diagnosis of DSM-5ADHD combined, predominantly inattentive or hyperactive/impulsive
presentation, per clinical evaluation and confirmed by the MINI-KID

5. Clinical Global Impressions-Severity (CGI-S) ≥ 3

6. ≥ 90th percentile normative value for gender and age on the ADHD RS-IV total score at
screening or baseline

7. Study participant has a parent/legal guardian who is willing and able to give written
informed consent for him/her to participate in the study

8. Study participant must be able to give assent to participate in the trial

9. Study participant and legal guardian must be able to speak and understand English

10. Able to tolerate multiple finger pricks

11. Willing to comply with all study procedures

Exclusion Criteria:

1. Current (last month) psychiatric diagnosis other than specific phobia, motor skills
disorders, oppositional defiant disorder, sleep disorders, elimination disorders,
adjustment disorders, learning disorders, or communication disorders. Participants
with school phobia or separation anxiety will not be eligible

2. Cognitively impaired, in the investigator's opinion

3. Any clinically significant chronic medical condition that, in the judgment of the
investigator, may interfere with the participant's ability to participate in the study

4. Seizure disorder excluding a history of febrile seizures

5. Thyroid disease

6. Tourette's disorder or chronic tic disorder (mild medication induced tics are allowed)

7. Serious cardiac condition including cardiomyopathy, serious arrhythmias, structural
cardiac disorders, or severe hypertension

8. Glaucoma

9. Current or recent (within the past 6 months) DSM-5 drug dependence or substance abuse
(excluding nicotine and caffeine)

10. Pregnant or nursing females. Females must have a negative urine pregnancy test at
screening as well as four additional visits and must be abstinent or use adequate and
reliable contraception throughout the study

11. Currently treated and satisfied with ADHD medication

12. Current psychotropic medications other than sedative hypnotics for sleep

13. Use of atomoxetine, clonidine, guanfacine or a monoamine oxidase inhibitor within 28
days of the baseline visit

14. Participation in another investigational medication study within 30 days prior to
screening

15. Clinically significant abnormal laboratory result, electrocardiogram (ECG) result,
physical examination, or vital signs at screening that the investigator considers to
be inappropriate to allow participation in the study

16. Planned use of prohibited drugs from the baseline visit through the end of the trial

17. History of allergic reaction or a known or suspected sensitivity to any substance that
is contained in the study drugs

18. Food allergies that are determined by the PI as too severe to be easily accommodated
for during the study

19. Inability to swallow study medication