The Efficacy and Safety of PRC-063 in Adult ADHD Patients

Completed · Phase 3 · Has a placebo group

Conditions studied: ADHD

In brief

The purpose of this randomized, placebo-controlled, double-blind, parallel group study is to evaluate the clinical efficacy and safety of PRC-063 in adults with ADHD

Key facts

Study ID

NCT02139124

Run by

Rhodes Pharmaceuticals, L.P.

People needed

375

Starts

2014-04-01

Expected to finish

2015-01-01

Last updated by the study team

2019-05-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or non-pregnant, non-nursing female at least 18 years of age and meeting the local, legal definition of adult.
• ADHD diagnosis, inattentive, hyperactive/impulsive or combined, as defined by the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) based on clinician assessment using multiple informants and a structured interview.
• Unsatisfied with his or her current pharmacological therapy for treatment of ADHD or not currently receiving pharmacological therapy for ADHD. Inclusion of subjects naïve to pharmacological therapy for ADHD is permitted.
• Female subjects must be one of the following: a. surgically sterile prior to screening; b.
• postmenopausal; c. if of childbearing potential, abstinent or willing to use a reliable method of contraception, such as oral contraceptive, two barrier methods, a barrier method plus a spermicidal agent.
• Female subjects of Child-Bearing Potential (FOCP) must have a negative serum β-hCG pregnancy test at screening.
• Minimum level of intellectual functioning, as determined by an Intelligence Quotient (IQ) score of 80 or above based on the WASI.
• Mentally and physically competent to sign an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.
• Able and willing to comply with the study procedures for the entire length of the study, including a successful swallow test of an empty 100 mg capsule.

You may not qualify if…

• Having an allergy to methylphenidate or amphetamines or a history of serious adverse reactions to methylphenidate.
• Known to be non-responsive to methylphenidate treatment. Non-response is defined as methylphenidate use at various doses for a phase of at least four weeks at each dose with little or no clinical benefit.
• Being diagnosed with or having a history of strokes, epilepsy, migraine headaches (greater than 1 instance every two months), glaucoma, thyrotoxicosis, tachyarrhythmias or severe angina pectoris or serious or unstable medical illness. Subjects with controlled or stable asthma or diabetes will be permitted.
• Elevated blood pressure, defined as any values above 89 diastolic or 139 systolic, as assessed at Visit 1.
• Clinically significant ECG abnormalities, as assessed at Visit 1.
• Clinically significant laboratory abnormalities, as assessed at Visit 1.
• Currently receiving guanethidine, pressor agents, MAO inhibitors, coumarin anticoagulants, anticonvulsants (e.g. phenobarbital, phenytoin, primidone), phenylbutazone, tricyclic antidepressants (e.g. imipramine, desipramine), selective serotonin reuptake inhibitors (SSRIs) or herbal remedies (unless on a stable dose for 4 weeks).
• Subject has known history of symptomatic cardiovascular disease, advanced arteriosclerosis, structural cardiac abnormality, cardiomyopathy, serious heart rhythm abnormalities, coronary heart disease, transient ischemic attack or stroke or other serious cardiac problems that may place the subject at increased vulnerability to the sympathomimetic effects of a stimulant drug.
• Subject has a known family history of sudden cardiac death or ventricular arrhythmia.
• Subjects who are currently considered a suicide risk by the investigator.
• Having a primary diagnosis of schizophrenia, schizoaffective disorder, primary affective disorder, schizotypal personality, major depression, bipolar disorder, generalized anxiety, borderline personality disorder, antisocial personality or another unstable psychiatric condition requiring treatment, as assessed by the structured interview conducted at Visit 1.
• Having a history or suspected physiological dependence (excluding nicotine) on narcotic analgesics or other psychoactive drugs (including barbiturates, opiates, cocaine, cannabinoids, amphetamines and benzodiazepines).
• Excessive consumption of alcohol (consumes alcohol in quantities greater than 15 drinks per week; 1 drink is defined as 360 mL/12 oz. of beer, 120 mL/4 oz. of wine, or 30 mL/1 oz. of hard liquor), or history (within previous 6 months) of alcohol abuse.
• Currently (or within 30 days before the planned start of treatment) receiving an investigational drug or using an experimental medical device.
• Homeless.

Where it is running

• UCLA — Los Angeles, California, United States
• Synergy Clinical Research — National City, California, United States
• Newport Beach Clinical Research Associates, Inc. — Newport Beach, California, United States
• Orange County Neuro Phychiatry Research Centre — Orange, California, United States
• Florida Clinical Research Center — Bradenton, Florida, United States
• Sarkis Clinical Research — Gainesville, Florida, United States
• Sarkis Clinical Trials — Gainesville, Florida, United States
• CNS Healthcare Jacksonville — Jacksonville, Florida, United States
• Florida Clinical Research Center — Maitland, Florida, United States
• Clinical Neuroscience Solutions — Orlando, Florida, United States
• Stedman Clinical Trials — Tampa, Florida, United States
• Advanced Clinical Research — Boise, Idaho, United States
• Center for Psychiatry and Behavioral Medicine Inc. — Las Vegas, Nevada, United States
• Princeton Medical Institute — Princeton, New Jersey, United States
• Medical Research Network — New York, New York, United States
• Wake Research Associates — Raleigh, North Carolina, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• IPS Research Company — Oklahoma City, Oklahoma, United States
• Oregon Center for Clinical Investigation — Portland, Oregon, United States
• Oregon Center for Clinical Investigation — Salem, Oregon, United States
• Clinical Neuroscience Solutions Inc. — Memphis, Tennessee, United States
• FutureSearch Clinical Trials, L.P. — Austin, Texas, United States
• FutureSearch Trials of Dallas, L.P. — Dallas, Texas, United States
• Bayou City Research Ltd — Houston, Texas, United States
• Red Oak Psychiatry Associates — Houston, Texas, United States

Full record on ClinicalTrials.gov

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