Briefly, this was a randomized, double-blind, placebo-controlled trial assessing the efficacy of OROS-MPH compared to placebo for increasing smoking cessation rate among adult smokers with ADHD when added to nicotine patch and counseling. The study design consisted of an 11-week treatment phase with a four-week pre-quit phase and seven weeks of a planned abstinence period. All participants received a thorough explanation of the study from the investigators and signed an informed consent form. The trial was conducted at six sites (Cambridge, MA; Columbus, OH; New York City, NY (2 sites);

Temozolomide clinical trial Portland, OR; Rochester, MN) and approved by the Institutional Review Board at individual participating sites. Participants were given 21 mg/24 h nicotine patches from the target quit day (day 27) through week 11, received 14 mg/24 h patches for study weeks 12 and 13, and 7 mg/24 h patches for study week 14. Participants were randomized to OROS-MPH or matching placebo in a 1:1 ratio, with stratification by site, by a centralized, computerized system. For OROS-MPH the starting dose of 18 mg/day was escalated during the first two study weeks to a maximum of 72 mg/day or to the highest dose tolerated. Study participants received $25 Ruxolitinib molecular weight ($15 at one site)

per research visit; at the end-of-treatment visit (week 11) participants received an additional $25. More details of the study protocol, methods, and procedures are provided in the main outcome paper (Winhusen et al., 2010). Eligible participants were adults with ADHD who smoked at least 10 cigarettes per day, had an expired air carbon monoxide (CO) level ≥ 8 ppm, and smoked cigarettes regularly for at least 3 months prior to inclusion, wished to quit smoking, were in good physical for health as determined

by a medical history, electrocardiogram, vital signs and fulfilled DSM-IV criteria for ADHD as assessed by the Adult Clinical Diagnostic Scale version 1.2 (Adler and Cohen, 2004). The use of the parent study’s data and analysis was approved by the IRB of the New York State Psychiatric Institute, Columbia University. The ADHD Rating Scale (ADHD-RS; DuPaul et al., 1998 and Adler and Cohen, 2004) was used to assess DSM-IV ADHD symptoms. This instrument contains 18 individual items, 9 each reflecting inattention and hyperactivity/impulsivity. Each item is rated on a 4-point scale (never or rarely: 0, sometimes: 1, often: 2, very often: 4). The total score can range from 0 to 54, the maximum score for both inattention and hyperactivity/impulsivity subscales is 27. Cronbach’s α for the ADHD-RS at baseline was 0.86 in this study. ADHD symptoms were assessed at baseline (three to four weeks before a target quit date), and at weeks 2, 4, and 6 after the target quit date.