Behavior therapy can benefit most patients with attention deficit hyperactivity disorder (ADHD), but the vast majority of patients with the condition will still need pharmacotherapy to manage their symptoms and prevent the disorder from interfering with their lives. Yet little progress has been made in identifying effective agents for patients who don’t respond to the handful of existing medications.
“There are still pretty major gaps in optimal treatment of ADHD that potentially might be filled if we could find further ways of getting at the problem of ADHD,” said Glen Elliott, MD, PhD, chief psychiatrist and medical director of Children’s Health Council in Palo Alto, California. He noted that some interest has developed in GABA, a largely inhibitory neuroregulator, and glutamate, which is more excitatory, but not much has moved forward with these agents. Despite recent and continuing advances in understanding the condition, substantial knowledge gaps remain regarding ADHD’s etiology and neurobiology.
Russell Barkley, PhD, a clinical professor of psychiatry at the Medical University of South Carolina in Charleston, and a well-known clinician in the field, agreed, suggesting it might require more insight into genomic properties of the condition before any truly new drugs come along.
“Some companies tried to make a nicotinic receptor agent, but the ones I know of failed during their clinical trials, so that type of drug doesn’t seem useful to pursue any further,” Barkley said. “I think drug companies are awaiting further results from molecular genetic studies that show specific candidate genes for ADHD and that affect brain development and pathway functioning in such a way that a drug might be useful to try and intervene in that pathway, but none are close to commercial development.”
The market currently offers 2 US Food and Drug Administration (FDA)-approved stimulants, methylphenidate and amphetamine, and 3 FDA-approved nonstimulants: atomoxetine, a norepinephrine reuptake inhibitor, and two alpha agonists, clonodine and guanfacine. Aside from the various formulation options of these 5 agents and drugs prescribed off-label such as bupropion, not much else offers clinical value in treating patients with ADHD.
Even among these options, nonstimulants have a lower efficacy rate, estimated at 40% to 45% compared with 65% to 85% with the stimulants, Elliott pointed out. “With the two classes of stimulants we currently have, it doesn’t matter what stimulant you start with. It will be beneficial, well tolerated, and have the effects you’ll be looking for in 65% of people,” Elliott said. “If it doesn’t work, and you try the other class, another 20% will respond better or else the side effect profile is better.”
It is the remaining 15% of children and, increasingly, adults, who do not respond to any of the approved medications who really need novel therapies. There are also the disadvantages of stimulants, such as…