Study of ABX-1431 in Adult Patients With Tourette Syndrome or Chronic Motor Tic Disorder
Status:
Completed
Trial end date:
2020-01-20
Target enrollment:
Participant gender:
Summary
Two-part study consisting of a double-blind, randomized, placebo-controlled, study at two
target dose levels (Part 1) and an open-label, non-randomized study (Part 2) to determine the
efficacy of ABX-1431 in treating adult patients with Tourette syndrome or Chronic Motor Tic
Disorder as measured by the change from baseline in Total Tic Score of the Yale Global Tic
Severity Scale (YGTSS-TTS) compared with placebo.
Phase:
Phase 2
Details
Lead Sponsor:
Abide Therapeutics
Collaborators:
BASi (Bioanalytical Systems, Inc.) CogState Ltd. FGK Clinical Research GmbH