findmyKOL
Clinical trialNCT05273749CompletedPhase 3Interventional

A Phase 3 Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken Daily in Patients With Fibromyalgia

SponsorTonix Pharmaceuticals, Inc.Enrollment457Fibromyalgia
View the registry record on ClinicalTrials.gov

Summary

The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

33 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Tonix Clinical Site

    Phoenix, Arizona, United States

  • Tonix Clinical Site

    Oceanside, California, United States

  • Tonix Clinical Site

    Santa Ana, California, United States

  • Tonix Clinical Site

    Temecula, California, United States

  • Tonix Clinical Site

    Cromwell, Connecticut, United States

  • Tonix Clinical Site

    Fort Myers, Florida, United States

  • Tonix Clinical Site

    Jacksonville, Florida, United States

  • Tonix Clinical Site

    Miami Lakes, Florida, United States

  • Tonix Clinical Site

    Ocala, Florida, United States

  • Tonix Clinical Site

    Oldsmar, Florida, United States

  • Tonix Clinical Site

    Orlando, Florida, United States

  • Tonix Clinical Site

    Alpharetta, Georgia, United States

  • Tonix Clinical Site

    Atlanta, Georgia, United States

  • Tonix Clinical Site

    Evansville, Indiana, United States

  • Tonix Clinical Site

    West Des Moines, Iowa, United States

  • Tonix Clinical Site

    Prairie Village, Kansas, United States

  • Tonix Clinical Site

    Covington, Louisiana, United States

  • Tonix Clinical Site

    New Orleans, Louisiana, United States

  • Tonix Clinical Site

    Prairieville, Louisiana, United States

  • Tonix Clinical Site

    Boston, Massachusetts, United States

  • Tonix Clinical Site

    Gulfport, Mississippi, United States

  • Tonix Clinical Site

    Albuquerque, New Mexico, United States

  • Tonix Clinical Site

    Williamsville, New York, United States

  • Tonix Clinical Site

    Cincinnati, Ohio, United States

  • Tonix Clinical Site

    Tulsa, Oklahoma, United States

  • Tonix Clinical Site

    Portland, Oregon, United States

  • Tonix Clinical Site

    Charleston, South Carolina, United States

  • Tonix Clinical Site

    Austin, Texas, United States

  • Tonix Clinical Site

    Dallas, Texas, United States

  • Tonix Clinical Site

    McKinney, Texas, United States

  • Tonix Clinical Site

    Charlottesville, Virginia, United States

  • Tonix Clinical Site

    Danville, Virginia, United States

  • Tonix Clinical Site

    Kenosha, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
6 Apr 2022
Primary completion
14 Nov 2023
Completion
14 Nov 2023
Last update posted
22 Jan 2025
Registered enrollment
457
Registry id
NCT05273749

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.