Safety, Tolerability, PK & Efficacy of V81444 in Volunteers With Attention Deficit/ Hyperactivity Disorder (ADHD)

Completed · Phase 1/Phase 2 · Has a placebo group

Conditions studied: ADHD

In brief

The purpose of this research study is to evaluate the safety, tolerability, effectiveness, and pharmacokinetics (PK) of twice daily oral doses of V81444 in adults with ADHD. Pharmacokinetics (PK) is the study of how a drug is absorbed, distributed, metabolized, and eventually eliminated by the body. Pharmacokinetics is what the body does to the drug. Blood samples will be taken throughout the study for PK analysis.

Key facts

Study ID

NCT02253745

Run by

Vernalis (R&D) Ltd

People needed

31

Starts

2013-07-01

Expected to finish

2014-04-01

Last updated by the study team

2016-06-03

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must:
• Be male or female subjects aged 18 to 50 years inclusive
• Meet DSM-IV-TR criteria for a primary diagnosis of ADHD combined, hyperactive-impulsive or predominantly inattentive type; confirmed by a minimum score of 24 on the ADHD-RS with adult prompts:
• Have a body mass index (BMI) between 19 and 32 kg/m2 inclusive
• Be willing and able to comply with the requirements of the entire study
• Be able to read and understand English
• Give written informed consent

You may not qualify if…

• Have a significant medical condition or a history of such a condition that the Investigator considers should exclude the subject from the study
• Have any other significant psychiatric disorder, as determined by the Structured Clinical Interview for DSM-IV-TR Axis I Disorders (SCID-I)
• Have known mental impairment defined as an intelligence quotient (IQ) less than 75, or clinical evidence of mental impairment based on the opinion of the Investigator
• Have a history or evidence of clinically significant GI disease, including ulcers, gastro-esophageal reflux disease, hiatus hernia or gastritis
• Have had any previous gastric surgery and/or bariatric procedure
• Have any known malformations that would make EGD difficult or unsafe
• Have taken any prohibited concomitant medication
• Have multiple drug allergies or be allergic to any of the components of V81444 study medication or its matching placebo (see Section 7.1) or lidocaine
• Have abused drugs in the 12 months before study drug administration
• In the 90 days before study drug administration, on average
• have smoked more than 5 cigarettes per day
• have consumed more than 28 units of alcohol per week
• have consumed more than 500 mg of caffeine per day
• In the 2 calendar months before study drug administration
• have donated blood or plasma in excess of 500 mL
• been exposed to any new investigational agent
• In the calendar month prior to screening
• used non-steroidal anti-inflammatory drugs regularly
• had a new tattoo or body piercing
• Have any clinically relevant abnormal findings at Screening and/or admission
• Plan to undergo elective procedures/surgery at any time during the study
• Have any other condition that might increase the risk to the individual or decrease the chance of obtaining satisfactory data, as assessed by the Investigator.

Where it is running

• Vince and Associates Clinical Research — Kansas City, Kansas, United States

Full record on ClinicalTrials.gov

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