Safety and Efficacy of Vyvanse in Adults With Attention-Deficit/Hyperactivity Disorder

Completed · Phase 4 · Has a placebo group

Conditions studied: Attention-Deficit/Hyperactivity Disorder

In brief

The primary objective of this study is to evaluate the maintenance of efficacy, as measured by Adult ADHD Rating Scale with Prompts (Adult ADHD-RS with prompts) and Clinical Global Impression - Severity (CGI-S) scores, through a randomized withdrawal design when subjects with ADHD have been on stable treatment with commercial SPD489 for a minimum of 6 months and are maintained on their screening dose of commercial SPD489.

Key facts

Study ID: NCT00877487
Run by: Shire
People needed: 123
Starts: 2009-04-30
Expected to finish: 2010-07-08
Last updated by the study team: 2021-06-22

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject must be 18-55 years of age, inclusive at the time of consent.
Female subjects must have a negative serum beta Human Chorionic Gonadotropin (HCG) pregnancy test at Screening and a negative urine pregnancy test at baseline and agree to comply with any applicable contraceptive requirements of the protocol.
Subject has a documented diagnosis of ADHD or meets DSM-IV-TR™ with adult prompts criteria by history for a primary diagnosis of ADHD prior to treatment.
Subject has a Baseline score of <22 using the Adult ADHD-RS with prompts and CGI-S score ≤3.
Subject has been on stable treatment with commercial SPD489 (30, 50, or 70mg) for a minimum of at least 6 months preceding the Screening Visit with acceptable tolerability.Prior treatment with commercial SPD489 in the 6 months preceding the Screening Visit must be documented by prescription records, prescribing physician notes, or pharmacy records. Those subjects whose primary care physician (PCP) is someone other than the Principal Investigator (PI) will be required to provide the above documentation to the site.
Subject must have a minimum level of intellectual functioning, as determined by the Investigator.
Subject is willing and able to comply with all the testing and requirements defined in this protocol.
Subject is able to swallow a capsule.
Subject must be able to provide written, personally signed and dated informed consent to participate in the study, in accordance with the International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) Guideline E627 and applicable regulations, before completing any study-related procedures.

You may not qualify if…

Subject has a current comorbid psychiatric disorder that is either controlled with medications prohibited in this study or is uncontrolled and associated with significant symptoms. Prohibited disorders include those associated with diagnoses including but not limited to any severe comorbid Axis II disorder or severe Axis I disorder (such as Post Traumatic Stress Disorder [PTSD], psychosis, bipolar illness, pervasive developmental disorder, severe obsessive compulsive disorder, severe depressive or severe anxiety disorder). Other symptomatic manifestations (such as agitated states)that contraindicate treatment with SPD489 or confound efficacy or safety assessments in the opinion of the examining physician are also prohibited. Comorbid psychiatric diagnoses will be established by the psychiatric evaluation that includes the Structured Clinical Interview for DSM-IV-TR™ disorders (SCID-I).
Subject is currently considered a suicide risk, has previously made a suicide attempt or has a prior history of, or is currently demonstrating suicidal ideation.
The subject has a body mass index (BMI) of <18.5 or ≥40.
Subject has a concurrent chronic or acute illness (such as severe allergic rhinitis or an infectious process requiring antibiotics), disability, or other condition that might confound the results of safety assessments administered in the study or that might increase risk to the subject. Similarly, the subject will be excluded if he or she has any additional condition(s) that in the Investigator's opinion would prohibit the subject from completing the study or would not be in the best interest of the subject. This would include any significant illness or unstable medical condition that could lead to difficulty complying with the protocol. Mild, stable asthma is not exclusionary.
Subject has a history of seizures (other than infantile febrile seizures), any tic disorder, or a current diagnosis and/or a known family history of Tourette's Disorder.
Subject has known history of symptomatic cardiovascular disease, advanced arteriosclerosis, structural cardiac abnormality, cardiomyopathy, serious heart rhythm abnormalities, coronary artery disease, transient ischemic attack or stroke or other serious cardiac problems that may place them at increased vulnerability to the sympathomimetic effects of a stimulant drug.
Subject has a known family history of sudden cardiac death or ventricular arrhythmia.
Subject has any clinically significant ECG or clinically significant laboratory abnormality at Screening.
Subject has current abnormal thyroid function, as defined as abnormal Screening thyroid stimulating hormone (TSH) and thyroxine (T4). Treatment with a stable dose of thyroid medication for at least 3 months is permitted.
Subject has a history of moderate to severe hypertension or has a resting sitting systolic blood pressure >139mmHg or diastolic blood pressure >89mmHg. Subjects with well-controlled mild or moderate hypertension on a single antihypertensive agent are allowed.
Subject is taking any medication that is excluded (Please refer to Table 2).
Subject has a documented allergy, hypersensitivity, or intolerance to amphetamines.
Subject has a recent history (within the past 6 months) of suspected substance abuse or dependence disorder (excluding nicotine) in accordance with DSM-IV-TR™ criteria.
Subject has a positive urine drug result at Screening (with the exception of subject's current stimulant therapy).
Subject has taken an investigational compound that has a central nervous system(CNS) effect or taken part in a clinical trial for ADHD 6 months prior to the Screening Visit.
Subject has taken part in an investigational trial within the 30 days prior to the Screening Visit.
Subject has glaucoma.
Subject is taking other medications that have CNS effects or affect performance, such as chronic use of sedating antihistamines and decongestant sympathomimetics (7 days prior to Screening). Stable use of bronchodilator inhalers is not exclusionary.
Subject is female and pregnant or lactating.
Subjects who have previously been enrolled into this study and subsequently withdrawn.
Subject is not well controlled on SPD489 with acceptable tolerability (Adult ADHD-RS with prompts score ≥22).

Where it is running

Valley Clinical Research, Inc. — El Centro, California, United States
Peninsula Research Associates, Inc — Rolling Hills Estates, California, United States
PCSD Feighner Research — San Diego, California, United States
Elite Clinical Trials, Inc. — Wildomar, California, United States
Colorado Clinica Trials, Inc. — Highlands Ranch, Colorado, United States
Florida Clinical Research Center — Bradenton, Florida, United States
Gulfcoast Clinical Research Center — Fort Myers, Florida, United States
Clinical Neuroscience Solutions Inc — Jacksonville, Florida, United States
Fidelity Clinical Research, Inc. — Lauderhill, Florida, United States
CNS Healthcare — Orlando, Florida, United States
Miami Research Associates — South Miami, Florida, United States
Janus Center for Psychiatric Research — West Palm Beach, Florida, United States
Atlanta Center for Medical Research — Atlanta, Georgia, United States
Northwest Behavioral Research Center — Roswell, Georgia, United States
Joliet Center for Clinical Research — Joliet, Illinois, United States
Capstone Clinical Research — Libertyville, Illinois, United States
CIENTIFICA, Inc — Newton, Kansas, United States
Psychiatric Associates — Overland Park, Kansas, United States
Vince and Associates Clinical Research — Overland Park, Kansas, United States
Clinical Trial Technology Inc. — Prairie Village, Kansas, United States
Pedia Research LLC — Owensboro, Kentucky, United States
Four Rivers Clinical Research — Paducah, Kentucky, United States
Study site — Rockville, Maryland, United States
Rochester Center for Behavioral Medicine — Rochester Hills, Michigan, United States
Clinical Study Centers, LLC — Little Rock, Arkansas, United States

Full record on ClinicalTrials.gov

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