
Triple-bead mixed amphetamine salts (MAS), an investigational formulation of MAS designed for once-daily dosing, significantly improves symptoms of attention-deficit/hyperactivity disorder in adults, according to findings from 2 Phase III trials.
The double-blind trials enrolled adults aged 18 to 55 years with ADHD. In ...[more]
Initial data from the Multimodal Treatment Study of Children with ADHD (MTA) provided information about the efficacy of different treatments and treatment combinations in pediatric attention-deficit/hyperactivity disorder. Now, with 8-year follow-up data available, the MTA offers insight into the long-term outcomes of ADHD, including ...[more]
The stigma surrounding attention-deficit/hyperactivity disorder is prevalent and may influence adolescent and caregiver treatment decisions, but clinicians can use this information to select the most appropriate treatment plan, a panel advised.
Several of the panel speakers focused on ADHD-related stigma and presented ...[more]
Triple-bead mixed amphetamine salts (MAS), an investigational formulation of MAS designed for once-daily dosing, significantly improves symptoms of attention-deficit/hyperactivity disorder in adults, according to findings from 2 Phase III trials.
The double-blind trials enrolled adults aged 18 to 55 years with ADHD. In ...[more]
Initial data from the Multimodal Treatment Study of Children with ADHD (MTA) provided information about the efficacy of different treatments and treatment combinations in pediatric attention-deficit/hyperactivity disorder. Now, with 8-year follow-up data available, the MTA offers insight into the long-term outcomes of ADHD, including ...[more]
Phase II data confirm the safety profile of guanfacine extended release (XR) in children and adolescents with attention-deficit/hyperactivity disorder and suggest that the drug may increase evening sleepiness in these patients, but it does not increase daytime sleepiness in the classroom.
The current analysis was ...[more]
Dexmethylphenidate extended release is effective in treating children with attention-deficit/hyperactivity disorder, according to the results of a double-blind, fixed-dose titration trial.
Researchers randomized 253 pediatric patients aged 6 to 12 years with ADHD to 1 of 4 treatment arms. Following a washout period, ...[more]
Children with attention-deficit/hyperactivity disorder may be more likely than children without ADHD to experience specific functional deficits in young adulthood, data suggest.
The authors of the current analysis noted that recent research has begun to investigate outcomes in ADHD other than those related strictly to ...[more]
Adult patients with attention-deficit/hyperactivity disorder demonstrate significant improvements in symptom control within a week of taking lisdexamfetamine, Phase III trial data show.
The double-blind, dose-escalation study included 420 adults aged 18 to 55 years who met DSM-IV-TR criteria for ADHD and whose diagnosis ...[more]
Caregivers of children with attention-deficit/hyperactivity disorder--especially those of children who are taking drug therapy--experience significantly more emotional strain and poorer physical and mental health status than do caregivers of children without ADHD, a study found.
For this investigation, 2,036 caregivers ...[more]
Clinicians encounter several challenges when selecting which treatment may be optimal for patients with attention-deficit/hyperactivity disorder, but more research and new approaches could provide some guidance, according to several experts.
"I think what we want to highlight is that there are multiple factors that go ...[more]
Once-daily dosing with triple-bead mixed amphetamine salts (triple-bead MAS), an investigational treatment for attention-deficit/hyperactivity disorder, seems to improve ADHD symptoms in adolescents relative to placebo and demonstrates efficacy throughout a 16-hour treatment period, according to Phase II findings.
...[more]
Among adult smokers with attention-deficit/hyperactivity disorder, atomoxetine does not increase cigarette smoking, according to an analysis of Phase IV data. Additional findings suggest smoking status may affect the likelihood of treatment response in adults with ADHD.
The double-blind study included 218 adults aged 18 ...[more]
OROS methylphenidate is a safe and effective treatment for adult attention-deficit/hyperactivity disorder, according to an analysis of interim data from a long-term, open-label safety trial and data from a randomized, placebo-controlled, dose-titration study.
In the open-label safety study, OROS methylphenidate was ...[more]
Phase II data confirm the safety profile of guanfacine extended release (XR) in children and adolescents with attention-deficit/hyperactivity disorder and suggest that the drug may increase evening sleepiness in these patients, but it does not increase daytime sleepiness in the classroom.
The current analysis was ...[more]
Dexmethylphenidate extended release is effective in treating children with attention-deficit/hyperactivity disorder, according to the results of a double-blind, fixed-dose titration trial.
Researchers randomized 253 pediatric patients aged 6 to 12 years with ADHD to 1 of 4 treatment arms. Following a washout period, ...[more]
Children with attention-deficit/hyperactivity disorder may be more likely than children without ADHD to experience specific functional deficits in young adulthood, data suggest.
The authors of the current analysis noted that recent research has begun to investigate outcomes in ADHD other than those related strictly to ...[more]
Adult patients with attention-deficit/hyperactivity disorder demonstrate significant improvements in symptom control within a week of taking lisdexamfetamine, Phase III trial data show.
The double-blind, dose-escalation study included 420 adults aged 18 to 55 years who met DSM-IV-TR criteria for ADHD and whose diagnosis ...[more]
Caregivers of children with attention-deficit/hyperactivity disorder--especially those of children who are taking drug therapy--experience significantly more emotional strain and poorer physical and mental health status than do caregivers of children without ADHD, a study found.
For this investigation, 2,036 caregivers ...[more]
Clinicians encounter several challenges when selecting which treatment may be optimal for patients with attention-deficit/hyperactivity disorder, but more research and new approaches could provide some guidance, according to several experts.
"I think what we want to highlight is that there are multiple factors that go ...[more]
Once-daily dosing with triple-bead mixed amphetamine salts (triple-bead MAS), an investigational treatment for attention-deficit/hyperactivity disorder, seems to improve ADHD symptoms in adolescents relative to placebo and demonstrates efficacy throughout a 16-hour treatment period, according to Phase II findings.
...[more]
Among adult smokers with attention-deficit/hyperactivity disorder, atomoxetine does not increase cigarette smoking, according to an analysis of Phase IV data. Additional findings suggest smoking status may affect the likelihood of treatment response in adults with ADHD.
The double-blind study included 218 adults aged 18 ...[more]
OROS methylphenidate is a safe and effective treatment for adult attention-deficit/hyperactivity disorder, according to an analysis of interim data from a long-term, open-label safety trial and data from a randomized, placebo-controlled, dose-titration study.
In the open-label safety study, OROS methylphenidate was ...[more]