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A Phase 3, Double-Blind, Randomized, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily at Bedtime in Patients With Military-Related PTSD

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Trial Profile

A Phase 3, Double-Blind, Randomized, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily at Bedtime in Patients With Military-Related PTSD

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 22 Sep 2024

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At a glance

  • Drugs Cyclobenzaprine (Primary)
  • Indications Post-traumatic stress disorders
  • Focus Registrational; Therapeutic Use
  • Acronyms HONOR
  • Sponsors Tonix Pharmaceuticals Holding Corp

    • Most Recent Events

    • 21 Aug 2024 According to a Tonix Pharmaceuticals media release, data from this study and the AtEase study, evaluating TNX-102 in the Aftermath of Trauma to Reduce Acute Stress Disorder (ASD) and Prevent Military-Related PTSD , will be presented in a poster presentation on August 27, 2024, 3:00 p.m. - 5:00 p.m. ET, at the 2024 Military Health System Research Symposium (MHSRS), being held August 26-29, 2024, in Kissimmee, Fla.
    • 01 Apr 2024 Results published in the Psychiatry Research
    • 08 Mar 2024 According to a Tonix Pharmaceuticals media release,the company announced Publication in Psychiatry Research Showing Activity of Bedtime TNX-102 SL on PTSD Symptoms and Sleep Quality in Military-Related PTSD at Four Weeks of Therapy

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