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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT05472090

Public ClinicalTrials.gov record NCT05472090. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 31, 2026, 6:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, 14-week Double-Blind, Randomized, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily at Bedtime in Patients With Multisite Pain Associated With Post-Acute Sequelae of SARS-CoV-2 Infection (PASC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2, randomized, parallel-group, double-blind, placebo-controlled, 14-week study designed to evaluate the efficacy and safety of TNX-102 SL 5.6 mg (2 x 2.8 mg tablets) taken once daily at bedtime for the management of multi-site pain associated with Long COVID.

Study identification

NCT ID
NCT05472090
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tonix Pharmaceuticals, Inc.
Industry
Enrollment
63 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 18, 2022 (Actual)
Primary completion
Jul 12, 2023 (Actual)
Completion
Jul 27, 2023 (Actual)
Last update posted
Nov 26, 2024

2022 – 2023

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
28
Facility City State ZIP Site status
Accel Research-Birmingham Clinical Research Unit Birmingham Alabama 35216 —
Tonix Clinical Site Oceanside California 92056 —
Tonix Clinical Site Santa Ana California 92705 —
Tonix Clinical Site Centennial Colorado 80112 —
Tonix Clinical Site Aventura Florida 33180 —
Tonix Clinical Site Fort Myers Florida 33912 —
Tonix Clinical Site Orlando Florida 32801 —
Tonix Clinical Site St. Petersburg Florida 33709 —
Tonix Clinical Site Alpharetta Georgia 30022 —
Tonix Clinical Site Atlanta Georgia 30329 —
Tonix Clinical Site Chicago Illinois 60625 —
Tonix Clinical Site Des Moines Iowa 50265 —
Tonix Clinical Site Iowa City Iowa 52242 —
Tonix Clinical Site Prairie Village Kansas 66208 —
Tonix Clinical Site New Orleans Louisiana 70124 —
Tonix Clinical Site Prairieville Louisiana 70769 —
Tonix Clinical Site Boston Massachusetts 02115 —
Tonix Clinical Site Boston Massachusetts 02131 —
Tonix Clinical Site Methuen Massachusetts 01844 —
Tonix Clinical Site Gulfport Mississippi 39503 —
Tonix Clinical Site Albuquerque New Mexico 87109 —
Tonix Clinical Site New York New York 10036 —
Tonix Clinical Site Williamsville New York 14221 —
Tonix Clinical Site Shelby North Carolina 28150 —
Tonix Clinical Site Columbus Ohio 43215 —
Tonix Clinical Site Dayton Ohio 45432 —
Tonix Clinical Site Tulsa Oklahoma 74133 —
Tonix Clinical Site Austin Texas 78737 —
Tonix Clinical Site McKinney Texas 75070 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05472090, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 26, 2024 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05472090 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →