Neurovance’s EB-1020 SR For Adult ADHD Shows Stimulant-Like Efficacy In Phase 2a Trial
Data presented at Society of Biological Psychiatry 69th Annual Scientific Meeting; lays groundwork for EB-1020 SR as a potential treatment option for adult ADHD
Neurovance, Inc. today announced complete results from its phase 2a pilot study of EB-1020 SR, a non-stimulant, in adult male patients with all subtypes of ADHD (attention deficit hyperactivity disorder). EB-1020 SR is a norepinephrine- and dopamine-preferring triple reuptake inhibitor. The data showed a statistically significant improvement in ADHD symptoms on the ADHD-Rating Scale-IV (ADHD-RS-IV), the primary outcome measure, in a range similar to that reported in previously published trials with stimulants. EB-1020 SR appears to be well tolerated at the doses studied. If these results are replicated in larger trials, EB-1020 SR could be among the first non-stimulants to challenge stimulants for broad use in ADHD. Results were presented at the Society of Biological Psychiatry 69th Annual Scientific Meeting in New York.
“These data indicate that EB-1020 SR has the potential to be the first non-stimulant with efficacy similar to stimulants,” said Anthony A. McKinney, President and CEO of Neurovance. “This is important because stimulants are the most effective medications used to treat ADHD today, yet they carry a risk of abuse and diversion. Evidence in validated animal models suggests that EB-1020 SR carries less risk of reward. We are now moving ahead with a human abuse liability study to evaluate whether EB-1020 demonstrates less risk of abuse or diversion than the standard dose of d-amphetamine in known stimulant users, and expect results by the fourth quarter of this year.”
Adult ADHD is a very serious medical condition. A recent study showed drivers with ADHD are nearly 50% more likely to be in a serious car crash. The inattention and impulsivity associated with ADHD contribute to higher rates of incarceration, unemployment and unwanted pregnancies. Adult ADHD is often associated with serious psychiatric comorbidities, including depression, anxiety and substance abuse, which may have negative long-term consequences in patients’ lives.
Timothy E. Wilens, MD, of Massachusetts General Hospital, leading ADHD expert, senior advisor for the clinical trial and lead presentation author, said, “As many as 10 million American adults are diagnosed with ADHD, an important condition that results in disabling levels of inattention, distraction and impulsive actions, yet only one patient in ten is receiving treatment. This is clear evidence of the need for safe and effective therapeutics without the inconvenience and restrictions of controlled substances.”
The final phase 2a data were presented in a poster, “A Pilot Study of a Novel Monoamine Triple Reuptake Inhibitor EB-1020 SR in the Treatment of ADHD in Adults,” at the Society of Biological Psychiatry 69th Annual Scientific Meeting in New York.