Craig Erickson

Associate Professor Cincinnati Children’s Hospital

Dr. Erickson has worked to obtain continuous federal, foundation, internal, and industry funding supporting his and his collaborators’ research over the last 10 ten years of his career. He is the inventor or co-inventor on many patents focused on translational treatment development in neurodevelopmental disorders that are held at Cincinnati Children’s Hospital Medical Center and at his previous employer the Indiana University School of Medicine. He is considered an international expert in the clinical treatment of fragile X syndrome and has similar expertise in fragile X-specific clinical trial development. Dr. Erickson is additionally an avid teacher of future generations of child psychiatrists has received several teaching awards for his work in physician education. He also enjoys mentoring junior faculty in the behavioral and developmental neuropsychiatry sub-field of child psychiatry.
Specifically in research, he and his colleagues have moved forward several repurposed molecules for study in fragile X syndrome and autism spectrum disorder including work with acamprosate, riluzole, ketamine, D cycloserine, and N acetyl cysteine among other repurposed molecules. He also is working now to move several novel molecules into autism and fragile X-specific study using proprietary compounds abandoned from initially intended use that may hold promise in the disorders which he and his colleagues study.

Seminars

Tuesday 15th September 2026
Decision Grade EEG Biomarkers to De Risk Early Neuropsychiatric Drug Development: Case Study in Fragile X & Schizophrenia
1:00 pm
  • Using EEG as a sensitive, translational readout of drug-target engagement in small first in human studies across Fragile X, schizophrenia, and other brain disorders
  • Demonstrating rapid rescue and normalisation of disease relevant EEG signals following acute dosing and linking these changes to clinically meaningful cognitive outcomes
  • Pairing EEG biomarkers with regulatory acceptable endpoints, including NIH Toolbox measures, to strengthen confidence in early proof of concept
  • Applying EEG based responder identification to de risk progression into larger Phase 2 and 3 trials across heterogeneous neuropsychiatric populations
Craig Erickson