ABVC BioPharma announces update for ADHD Phase IIb study

ABVC BioPharma announced an update on the Company’s eight-week long ADHD Phase IIb clinical study taking place at the University of California San Francisco, UCSF, Medical Center and five Taiwanese medical centers. Sixty-nine subjects enrolled in the study, 50 completed the study, and 11 are currently undergoing treatment. The study entitled “A Phase IIb Study of PDC-1421 Capsule to Evaluate the Safety and Efficacy in Patients with Adult Attention-Deficit/Hyperactivity Disorder” is a randomized, double-blind, placebo-controlled study involving a total of approximately 100 patients in the United States and Taiwan. The Phase IIb clinical study continues the Phase IIa clinical study of ABV-1505. “We received a favorable response from the subjects participating in our ADHD Phase IIb study at all of our sites,” said ABVC BioPharma Chief Executive Officer Uttam Patil, Ph. D. “To reach an interim analysis, the study requires 69 patients’ data. Our clinical trials continue to demonstrate that medicine derived from plants can have significant therapeutic benefits, often with few – if any – side effects. We expect to report similar results in our interim analysis report.”