> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/company/tonix-pharmaceuticals-inc-77c18664-d1aa-472e-a5ca-82a7bf1500d4
> Record changed: 2026-10-13

# Tonix Pharmaceuticals, Inc.

Registry sponsor category

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Names and classification

**Other names**

- Tonix Pharmaceuticals, Inc.

**Company name**

Tonix Pharmaceuticals, Inc.

**Organisation type**

Industry

**Registry sponsor category**

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

**Website**

http://www.tonixpharma.com

Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q39052499)

## Location and listing

**Publicly traded (proxy)**

No

**Listing at source**

Listed

## Identifiers

**Wikidata ID**

Q39052499

Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q39052499)

## Related records

### Trials (39)

- (TNX-1500) in Kidney Transplant Recipients
- 12-Month Open-Label Long-term Safety Study of TNX-102 SL Tablets in Fibromyalgia Patients
- 12-Week Open-Label Extension Study of TNX-102 SL in PTSD Patients
- A 3-Month Open-Label Safety and Efficacy Study of TNX-102 SL Tablets in Fibromyalgia Patients
- A 40-week Study to Evaluate TNX-102 SL 5.6 mg Taken Daily at Bedtime in Patients With PTSD
- A Comparative Bioavailability and Pharmacokinetic Study of TNX-102 2.4 mg and Cyclobenzaprine 5 mg Tablets in Healthy Adults.
- A Phase 1, Open-Label, Parallel-Group, Single-Dose Study To Compare The Pharmakokinetics Of TNX-102 SL (Cyclobenzaprine Hydrochloride Sublingual Tablet) In Non-Elderly Versus Elderly Participants
- A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TNX-1500 in Healthy Subjects
- A Phase 2 Study to Evaluate the Efficacy and Safety of TNX-102 SL in Patients With Multi-Site Pain Associated With Post-Acute Sequelae of SARS-CoV-2 Infection
- A Phase 3 Study to Evaluate the Efficacy and Safety of TNX-102 SL in Participants With PTSD
- A Phase 3 Study To Evaluate The Efficacy And Safety Of TNX-102 SL In Patients With Fibromyalgia
- A Phase 3 Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily in Patients With Fibromyalgia
- A Single-Dose, Randomized, Open-Label, 2-Way Crossover Study to Evaluate the Dose-Proportionality, Safety, and Tolerability of TNX-102 SL (Cyclobenzaprine HCl Sublingual Tablets) in Healthy Japanese and Chinese Subjects
- A Study to Evaluate eFFIcacy and Safety of Sublingual TNX-102 SL Tablet Taken at Bedtime in Patients With fibRoMyalgia
- A Study To Evaluate The Efficacy And Safety Of TNX-102 SL In Patients With Fibromyalgia
- A Study to Evaluate the Efficacy and Safety of TNX-1900 in Patients With Chronic Migraine
- [A Study to Evaluate TNX-102 SL Monotherapy Versus Placebo in Participants With Major Depressive Disorder (MDD)](https://trialight.com/data/trial/a-study-to-evaluate-tnx-102-sl-monotherapy-versus-placebo-in-75d7ecca-34fa-4150-9930-3e6bc646568d.md)
- An Open-Label, Randomized Pilot Study Comparing the Safety of a Single Dose of TNX-1300 to Usual Care (UC) Alone for the Treatment of Signs and Symptoms of Acute Cocaine Intoxication in Male Emergency Department (ED) Subjects
- Assessment of Delayed-type Hypersensitivity Reactions to SARS-CoV-2 Peptide Antigens
- BEdtime Sublingual TNX-102 SL as Fibromyalgia Intervention Therapy (BESTFIT)

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