Study Overview

  • Study directors: Kevin Shapiro, MD PhD, and Elysa Marco, MD 

  • Recruiting: Yes 

  • Study Title: A double-blind, placebo-controlled, phase IIb, multi-center, 12-week prospective study to evaluate the efficacy and safety of gemlapodect in adult and adolescent patients with Tourette’s Syndrome 

  • Condition: Tourette’s Syndrome 

  • Purpose: The purpose of this study is to find out whether gemlapodect, an investigational medication, can reduce tics in individuals with Tourette’s Syndrome. 

Eligibility 

Inclusion criteria

  • 18 years old and above 

  • Diagnosed (or suspected) Tourette’s Syndrome 

  • Moderate-to-severe motor and vocal tics 

Exclusion criteria

  • Uncontrolled seizure disorders 

  • Unstable medical or psychiatric illness 

  • Conditions such as functional tic-like disorder, Huntington’s chorea, malignant TS, autism, severe anxiety, bipolar disorder, schizophrenia, or Parkinson’s disease 

  • Current CBT, CBiT, or neurostimulation 

  • Current use of medications for tics – contact our study team to discuss 

Noema Study

What is Involved? 

  • Testing: Comprehensive tic assessments, psychiatric questionnaires, and medical evaluations 

  • Frequency of visits: 8 visits over 4 months 

  • Costs: No costs will be charged for any of the study procedures 

  • Payment: In return for the time, effort, and travel expenses, participants will be compensated $100 per visit 

Location and Contact Information 

Cortica Marin