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Trial record 2 of 4 for:    Imc-1

Fibromyalgia Outcome Research Trial Evaluating Synergistic Suppression of HSV-1 (FORTRESS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT04748705
Recruitment Status : Recruiting
First Posted : February 10, 2021
Last Update Posted : August 24, 2021
Information provided by (Responsible Party):
Virios Therapeutics, Inc.

Brief Summary:
Randomized, double-blind, placebo-controlled, 16-week study designed to explore the safety and efficacy of IMC-1 for the treatment of patients with fibromyalgia.

Condition or disease Intervention/treatment Phase
Fibromyalgia Drug: IMC-1 Drug: Placebo BID Tablet Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 460 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Double-Blinded, Randomized, Placebo-Controlled, Phase 2B Trial of IMC-1 for the Treatment of Fibromyalgia
Actual Study Start Date : June 3, 2021
Estimated Primary Completion Date : June 2022
Estimated Study Completion Date : July 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Fibromyalgia

Arm Intervention/treatment
Experimental: IMC-1 Oral Tablet
2X IMC-1 Tablet taken orally, each morning and evening.
Drug: IMC-1
Patients will take 1 tablet twice daily, each morning and evening, of randomly assigned study drug orally starting on Day 1 through study duration.

Placebo Comparator: Placebo
2X Placebo Tablet taken orally, each morning and evening.
Drug: Placebo BID Tablet
Patients will take 1 tablet twice daily, each morning and evening, of randomly assigned study drug orally starting on Day 1 through study duration.

Primary Outcome Measures :
  1. Mean Pain Score [ Time Frame: 16 Week ]
    Change from Baseline to Week 16 endpoint in the diary Numerical Rating Scale (NRS) weekly average of daily self-reported average pain severity scores. Scores range from 0 to 10 where a higher score means worse outcome.

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • The patient is female, 18 to 65 years of age, inclusive.
  • The patient has a diagnosis of primary FM as defined by the 2016 Revisions to the 2010/2011 fibromyalgia diagnostic criteria (American College of Rheumatology Preliminary Diagnostic Criteria)
  • The in clinic 7-day recall VAS scale average daily pain intensity score at Screening visit within protocol defined range.

Exclusion Criteria:

  • Any underlying medical or psychiatric condition that could impact their safe participation per protocol.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT04748705

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Contact: Channing Gray, MS (866)-620-8655

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United States, Alabama
IMC Study Site Recruiting
Birmingham, Alabama, United States, 35216
United States, Arkansas
IMC Study Site Recruiting
Rogers, Arkansas, United States, 72758
United States, California
IMC Study Site Recruiting
Beverly Hills, California, United States, 92602
IMC Study Site Recruiting
Oceanside, California, United States, 92056
IMC Study Site Recruiting
Riverside, California, United States, 92503
IMC Study Site Recruiting
Sacramento, California, United States, 95831
IMC Study Site Recruiting
San Diego, California, United States, 92103
IMC Study Site Recruiting
Santa Ana, California, United States, 92705
IMC Study Site Recruiting
Temecula, California, United States, 92591
United States, Florida
IMC Study Site Recruiting
Jacksonville, Florida, United States, 32256
IMC Study Site Recruiting
Oldsmar, Florida, United States, 34677
IMC Study Site Recruiting
Orlando, Florida, United States, 32801
IMC Study Site Recruiting
Tampa, Florida, United States, 33614
United States, Georgia
IMC Study Site Recruiting
Alpharetta, Georgia, United States, 30022
United States, Illinois
IMC Study Site Recruiting
Gurnee, Illinois, United States, 60031
United States, Indiana
IMC Study Site Not yet recruiting
Evansville, Indiana, United States, 47714
United States, Iowa
IMC Study Site Recruiting
Des Moines, Iowa, United States, 50265
United States, Kansas
IMC Study SIte Recruiting
Prairie Village, Kansas, United States, 66208
United States, Louisiana
IMC Study Site Recruiting
New Orleans, Louisiana, United States, 70124
IMC Study Site Recruiting
Prairieville, Louisiana, United States, 70769
United States, Massachusetts
IMC Study Site Recruiting
Boston, Massachusetts, United States, 02131
IMC Study Site Recruiting
North Dartmouth, Massachusetts, United States, 02747
IMC Study Site Recruiting
Quincy, Massachusetts, United States, 02169
United States, Mississippi
IMC Study Site Recruiting
Jackson, Mississippi, United States, 39202
United States, Nevada
IMC Study Site Recruiting
Las Vegas, Nevada, United States, 89102
United States, New Mexico
IMC Study Site Recruiting
Albuquerque, New Mexico, United States, 87109
United States, New York
IMC Study Site Recruiting
Cedarhurst, New York, United States, 11516
IMC Study Site Recruiting
Williamsville, New York, United States, 14221
United States, Ohio
IMC Study Site Recruiting
Cincinnati, Ohio, United States, 45219
IMC Study Site Recruiting
North Canton, Ohio, United States, 44720
United States, Oklahoma
IMC Study Site Recruiting
Oklahoma City, Oklahoma, United States, 73106
IMC Study Site Recruiting
Tulsa, Oklahoma, United States, 74133
United States, Oregon
IMC Study Site Recruiting
Salem, Oregon, United States, 97301
United States, Pennsylvania
IMC Study Site Recruiting
Allentown, Pennsylvania, United States, 18104
United States, Rhode Island
IMC Study Site Not yet recruiting
Warwick, Rhode Island, United States, 02886
United States, Tennessee
IMC Study Site Recruiting
Chattanooga, Tennessee, United States, 37421
IMC Study Site Not yet recruiting
Knoxville, Tennessee, United States, 37912
United States, Texas
IMC Study Site Recruiting
Austin, Texas, United States, 78737
IMC Study Site Recruiting
Dallas, Texas, United States, 75231
United States, Utah
IMC Study Site Recruiting
Salt Lake City, Utah, United States, 84102
United States, Virginia
IMC Study Site Recruiting
Charlottesville, Virginia, United States, 22911
United States, Washington
IMC Study Site Recruiting
Everett, Washington, United States, 98201
Sponsors and Collaborators
Virios Therapeutics, Inc.
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Responsible Party: Virios Therapeutics, Inc. Identifier: NCT04748705    
Other Study ID Numbers: PRID-202
First Posted: February 10, 2021    Key Record Dates
Last Update Posted: August 24, 2021
Last Verified: August 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: No: There is not a plan to make IPD available.

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Virios Therapeutics, Inc.:
Additional relevant MeSH terms:
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Myofascial Pain Syndromes
Muscular Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Neuromuscular Diseases
Nervous System Diseases