Tonix Pharmaceuticals is currently enrolling participants in a Phase 3 trial for military-related posttraumatic stress disorder.  For more information, please visit or (NCT03062540).

Research & Development
: Tonmya for PTSD

Tonmya for PTSD

TonmyaAttribution is a small, rapidly-disintegrating sublingual (under-the-tongue) tablet containing 2.8 mg of cyclobenzaprine HCl for daily bedtime use. Tonix is developing Tonmya at the 5.6 mg dose as a potential treatment for PTSD. In the AtEase Trial, Tonmya 5.6 mg taken sublingually at bedtime demonstrated efficacy (reduction in CAPS-5 score) and safety for the treatment of military-related PTSD compared to placebo (see below). Tonmya targets mechanisms which are associated with disturbed sleep and nightmares. It is believed that restoring deeper stages of sleep in PTSD may allow the body's natural recovery processes from severe trauma to be established, resulting in recovery from daytime symptoms of intrusion, pathological avoidance and agitation.

In December 2016, Tonmya was granted Breakthrough Therapy designation by the FDA for the treatment of PTSD.

Scientific Rationale

Sleep disturbances are core symptoms of PTSD. These disturbances are classified as 're-experiencing' symptoms when they manifest as distressing dreams and nightmares, and as 'hyperarousal' symptoms when insomnia or restless sleep are present. Poor sleep quality after a trauma is linked to the onset of PTSD and correlates with depression, substance abuse and suicide. As supported by prior clinical studiesFootnoteFootnote, Tonmya may have the potential to improve disturbed sleep and provide relief to the symptoms experienced by people with PTSD. Research by Tonix has shown that Tonmya acts on multiple neurotransmitter systems which relate to common sleep disturbances in PTSD:

  • Blocks the serotonin 2A receptor, associated with an increase in restorative slow wave sleep (SWS) and a decrease in waking-after-sleep-onset
  • Blocks the alpha-1 adrenergic receptor, associated with reducing trauma-related nightmares and sleep disturbance
  • Blocks the histamine-1 receptor, associated with the reversal of stress-induced increases in rapid eye movement (REM) sleep in preclinical studies

The active ingredient of Tonmya, cyclobenzaprine hydrochloride, has an extensive history of clinical use and is one of most widely-prescribed medications in the U.S. as an acute treatment for muscle spasm. As a sublingual, low-dose formulation for use at bedtime, Tonmya is designed to optimize the delivery and absorption of cyclobenzaprine for the treatment of PTSD. As cyclobenzaprine products have been approved only for short-term use, Tonmya is undergoing clinical development for long-term use.

Clinical Development

Tonix announced topline results of the Phase 2 dose-finding clinical study of Tonmya (cyclobenzaprine HCl sublingual tablets) in military-related PTSD (AtEase Study) on May 19, 2016.

The goal of the AtEase Study was to evaluate the potential clinical benefit of using Tonmya to treat military-related PTSD at a dose of 2.8 mg or 5.6 mg. The AtEase Study identified the 5.6 mg dose as a clinically effective and well-tolerated dose for registration studies. Tonmya 5.6 mg taken sublingually at bedtime demonstrated efficacy (reduction in CAPS-5 score) and safety for the treatment of military-related PTSD compared to placebo.

In a randomized, placebo-controlled study of 231 patients with PTSD at 25 U.S. clinical sites, a bedtime sublingual dose of 2.8 mg Tonmya (n=90) or 5.6 mg Tonmya (n=49) was compared to placebo (n=92) for the treatment of military-related PTSD. The retention rate was higher than typical for a PTSD clinical trial, since 73% completed the study on placebo, 79% on Tonmya 2.8 mg and 84% on Tonmya 5.6 mg. The primary efficacy endpoint was the 12-week mean change from baseline in the severity of PTSD symptoms as measured by the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) between those treated with Tonmya and those receiving placebo. The CAPS-5 is a standardized structured clinical interview and serves as the gold standard in research for measuring the symptom severity of PTSD.

This dose-finding study was designed to evaluate whether a 2.8 mg dose would be an efficacious dose and to provide an opportunity for this study to be one of the pivotal efficacy studies. Although the 2.8 mg dose trended in the direction of a therapeutic effect, it did not reach statistical significance on the primary endpoint. In contrast, the 5.6 mg dose had a therapeutic effect as assessed by the CAPS-5, which was statistically significant by analysis of covariance (ANCOVA) (p-value = 0.038), even though this arm of the study was designed to include half the number of patients of the 2.8 mg arm.

Tonmya 2.8 mg and 5.6 mg were well tolerated as evidenced by the high overall completion rate in the active treatment groups, which exceeded the completion rate in the placebo group.  The three treatment arms were well balanced on demographic characteristics. There were four distinct serious adverse events (SAEs); three were in the placebo group, and one (proctitis/peri-rectal abscess), in the Tonmya group, was reported to be unrelated to Tonmya.

Summaries of the preliminary efficacy and safety results are provided in the following tables:

Table 1. Preliminary Efficacy of Tonmya in the AtEase Study

Assessment Domain Analysis p Values
2.8 mg (N=90) 5.6 mg (N=49)
CAPS-5 Total MMRM1 with Multiple Imputation 0.211 0.031*
Total ANCOVA 0.090 0.038*
Arousal and Reactivity MMRM 0.141 0.048*
Sleep E6 Item MMRM 0.185 0.010*
Startle E4 Item MMRM 0.336 0.015*
CGI-I2 Responder 0.240 0.041*
PGIC3 MMRM 0.075 0.035*
Sheehan Disability Scale Total MMRM 0.174 0.079
Work/school Item MMRM 0.123 0.050*
Social/leisure Item MMRM 0.198 0.031*
Family life/home responsibilities Item MMRM 0.375 0.524

1MMRM = Mixed Model Repeated Measures
2CGI-I = Clinician Global Impression-Improvement
3PGIC = Patient Global Impression of Change
*p < 0.05

Table 2. Preliminary Adverse Events Reported in > 5% of Subjects in Any Treatment Arm

Placebo 2.8 mg 5.6 mg Total Tonmya
(N=94) (N=93) (N=50) (N=143)
Local Administration Site Conditions
   Hypoaesthesia oral 2 (2.1%) 36 (38.7%) 18 (36.0%) 54 (37.8%)
   Paraesthesia oral 3 (3.2%) 15 (16.1%) 2 (4.0%) 17 (11.9%)
   Glossodynia 1 (1.1%) 3 (3.2%) 3 (6.0%) 6 (4.2%)
Systemic Adverse Events
   Somnolence 6 (6.4%) 11 (11.8%) 8 (16.0%) 19 (13.3%)
   Dry mouth 10 (10.6%) 4 (4.3%) 8 (16.0%) 12 (8.4%)
   Headache 4 (4.3%) 5 (5.4%) 6 (12.0%) 11 (7.7%)
   Insomnia 8 (8.5%) 7 (7.5%) 3 (6.0%) 10 (7.0%)
   Sedation 1 (1.1%) 2 (2.2%) 6 (12.0%) 8 (5.6%)
   Upper respiratory infection 5 (5.3%) 3 (3.2%) 2 (4.0%) 5 (3.5%)
   Abnormal dreams 5 (5.3%) 1 (1.1%) 1 (2.0%) 2 (1.4%)
   Weight increased 5 (5.3%) 1 (1.1%) 1 (2.0%) 2 (1.4%)