Last updated on April 2019

A Phase 3 Study to Evaluate the Efficacy and Safety of TNX-102 SL in Participants With PTSD


Brief description of study

This is a 12-week, multicenter, randomized, double-blind, placebo-controlled, fixed-dose study that will investigate the efficacy and safety of TNX-102 SL 5.6 mg (2 x 2.8 mg tablets)

  • a sublingual formulation of cyclobenzaprine. Following successful screening and randomization, eligible patients will have a telephonic visit at week 2 and then return regularly to the study clinic for monthly visits for assessments of efficacy and safety.

Clinical Study Identifier: NCT03841773

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