Condition: Attention-deficit/Hyperactivity Disorder · Sponsor: NYU Langone Health
The goal of this study is to extend the efficacy evidence of sustained release methylphenidate compound (JornayPM) in adults with Attention-deficit/hyperactivity disorder (ADHD). JornayPM has recently been approved for treatment of patients 6 years and older with ADHD; the release mechanism is unique among ADHD products in that it is taken in the evening, with effects in the morning upon awakening and then throughout the subsequent day. Of note, to date, there is no clinical data as to the tolerability or clinical effects or dosing in adults with ADHD; therefore the primary aim of this trial is to gather the first set of these data.
This description comes directly from the study's public registry record.
Terry Leon, MS, RN · 646-754-4841 · Terry.Leon@nyulangone.org
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| NYU Langone Health | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06577779