Study of the Duration and Efficacy of MYDAYIS on Adult ADHD Symptoms and Executive Function In Early Evening

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Attention-deficit/hyperactivity Disorder
  • Age: Between 18 - 60 Years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Participants who meets DSM V-TR criteria for a primary diagnosis of ADHD

You may not be eligible for this study if the following are true:

    1. Participants meets DSM V-TR criteria for a primary diagnosis of hyperactive-impulsive type ADHD
    2. Those with any other current psychiatric disorder
    3. Participants who have suicidal ideation or history of suicide attempts
    4. Lifetime history of bipolar disorder or any psychotic disorder
    5. Pregnant, breastfeeding or women planning to become pregnant
    6. Participants with positive urine drug toxicology
    7. Any other reason that, in the opinion of the investigator, prevents the subject from participating in the study or compromise the subject safety

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.