Study Examining Repeat Dosing of OROS® Methylphenidate (CONCERTA®) and Immediate Release Methylphenidate in Healthy Adults

NCT00302393 | Completed Phase 3

• 1 other identifier: 2005-p-001811
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

There are two specific aims of this study. The first is to document the pharmacokinetics of dopamine transporter (DAT) receptor occupancy of repeated administration of orally administered, therapeutic doses of a short immediate release-methylphenidate hydrochloride (IR-MPH) and a long-acting formulation of MPH (OROS-MPH) using positron emission tomography (PET) scanning with C-11 altropane as the ligand. The investigators hypothesize that central nervous system (CNS) DAT occupancy of the OROS-MPH to IR-MPH sequence will be greater than that of IR-MPH to OROS-MPH sequence at 5 hours after the initial administration and that the CNS DAT occupancy of the other two formulations will be intermediate. The second aim of this study is to assess whether the abuse liability potential of delayed, repeated administrations of different formulations of MPH is moderated by the oral delivery system in which a delivery system with slower onset may be safer than one with more rapid early release.

Conditions

Healthy

Keywords

healthy volunteers

Outcome Measures

Primary Outcomes (1)

• The DAT receptor occupancy of OROS MPH and MPH IR using PET scanning with C-11 altropane. Objective measures also provided by d and l ritalinic acid and methylphenidate levels at pre-dose, hour 4, 5 and 6.

  The first visit will consist of a baseline PET scan during which no medication will be administered. For the next four study visits, subjects will be administered a first dose of one of the study treatments at hour 0 and then a second dose of one of the study treatments at hour 4. The study visits may be scheduled five to 30 days apart, but each subject must complete the five visits within a ten-week period.

  Eligible subjects will be asked to return to the study center for five study visits.

Study Arms (2)

IR-MPH

ACTIVE COMPARATOR

Immediate Release Methylphenidate administered before PET Scan

Drug: methylphenidate hydrochloride

Concerta

ACTIVE COMPARATOR

OROS Methylphenidate (Concerta) administered before PET Scan

Drug: OROS methylphenidate hydrochloride

Interventions

OROS methylphenidate hydrochloride DRUG

Subjects will be administered a first dose of one of the study treatments at hour 0 and then a second dose of one of the study treatments at hour 4 at each of the four treatment days in a crossover fashion, so that each subject will have received doses of each combination of treatments during the study. Each dose of OROS MPH will be 36 mg which will be supplied as one 36 mg capsules. Study treatments will be administered with water following an overnight fast of at least 8 hours.

Concerta

methylphenidate hydrochloride DRUG

Subjects will be administered a first dose of one of the study treatments at hour 0 and then a second dose of one of the study treatments at hour 4 at each of the four treatment days in a crossover fashion, so that each subject will have received doses of each combination of treatments during the study. Each dose of IR MPH will be 20 mg which will be supplied as one 20 mg capsule. Study treatments will be administered with water following an overnight fast of at least 8 hours.

IR-MPH

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Signed written informed consent to participate in the study
• Age: 18 - 55
• If female, non-pregnant, non-nursing, using an adequate form of birth control or a negative plasma pregnancy test
• Supine and standing blood pressure within the range 110/60 to 150/90 mmHg
• Heart rate, after resting for 5 minutes, within the range 46-90 beats/min
• Subjects who are within 20% of the ideal weight for height
• Right handed

You may not qualify if:

• Subjects with marked anxiety, tension, and agitation since the drug may aggravate these symptoms
• Subjects with known hypersensitivity to methylphenidate or other components of Concerta or Ritalin
• Subjects with glaucoma
• Subjects with motor tics or with a family history or diagnosis of Tourette's syndrome
• Subjects treated with monoamine oxidase inhibitors (MAOIs) or within 14 days of discontinuation of treatment with MAOIs
• 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.
• 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 et al 1961)
• Hamilton Anxiety Scale \> 21 (out of a possible 56 on the 14-item scale) (Hamilton 1959)
• Diagnosis of ADHD (attention deficit hyperactivity disorder)
• History of head trauma with loss of consciousness, organic brain disorders, seizures, or neurosurgical intervention
• Any clinically significant chronic medical condition, in the judgment of the investigator
• Mental impairment as evidenced by an intelligence quotient (I.Q.) \< 75
• Exposure to dopamine receptor antagonists within the previous three (3) months

Sponsors & Collaborators

• Massachusetts General Hospital: lead
• McNeil Consumer & Specialty Pharmaceuticals, a Division of McNeil-PPC, Inc.: collaborator

Study Sites (1)

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Location

MeSH Terms

Interventions

Methylphenidate

Intervention Hierarchy (Ancestors)

Phenylacetates; Acids, Carbocyclic; Carboxylic Acids; Organic Chemicals; Piperidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds

Study Officials

• Thomas Spencer, MD

  Massachusetts General Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: NONE
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant Director, Pediatric Psychopharmacology Unit

Study Record Dates

• First Submitted: March 10, 2006
• First Posted: March 14, 2006
• Study Start: June 1, 2006
• Primary Completion: February 1, 2007
• Study Completion: February 1, 2008
• Last Updated: October 22, 2013

Record last verified: 2013-10

Locations

US (1)