Item 7.01 Regulation FD Disclosure.
The below letter may be sent by Virios Therapeutics, Inc. (the “Company”) to its shareholders. This letter and the information therein may also be used, in whole or in part, by the Company from time to time with investors, analysts, collaborators, vendors or other third parties. In addition, a copy of this letter will be posted to the Company’s website.
The information in this Item 7.01 is furnished solely pursuant to Item 7.01 of Form 8-K. Consequently, such information is not deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, or otherwise subject to the liabilities of that section. Further, the information in this Item 7.01, including the exhibit, shall not be deemed to be incorporated by reference into the filings of the registrant under the Securities Act of 1933.
April 13, 2023
Dear Virios (VIRI) Shareholders,
We wanted to provide you with a succinct corporate progress report as we exit the first quarter of 2023, which can be summarized as follows:
| ● | We executed a very constructive end-of-Phase 2 meeting with FDA this past quarter with the goal of securing FDA guidance and agreement on our request to progress IMC-1 to Phase 3 development for fibromyalgia. |
| ● | We will provide updates as we receive FDA guidance regarding the required Phase 3 pivotal studies for this important FDA “Fast-track” designated program. |
| ● | We anticipate top line results from our ongoing IMC-2 exploratory combination antiviral Long-COVID trial in June. |
| ● | Through continued prudent expense management, we believe that the Company has capital to support general and administrative operations into Q2 of 2024. |
Warmest regards,
Greg Duncan
Chairman & CEO Virios Therapeutics, Inc.
About Virios Therapeutics, Inc
Virios Therapeutics (Nasdaq: VIRI) is a development-stage biotechnology company focused on advancing novel antiviral therapies to treat debilitating chronic diseases, such as fibromyalgia (“FM”). Immune responses related to the activation of tissue resident herpes have been postulated as a potential root cause triggering and/or sustaining chronic illnesses such as FM, irritable bowel disease, chronic fatigue syndrome and other functional somatic syndromes, all of which are characterized by waxing and waning symptoms with no obvious etiology. Our lead development candidate (“IMC-1”) is a novel, proprietary, fixed dose combination of famciclovir and celecoxib designed to synergistically suppress herpes virus replication, with the end goal of reducing virally promoted disease symptoms. IMC-1 has been granted fast track designation by the FDA.
The Company is pursuing a second development candidate, IMC-2 (valacyclovir and celecoxib), as a potential treatment for managing the fatigue, sleep, attention, pain, autonomic function and anxiety associated with Long-COVID, otherwise known as Post-Acute Sequelae of COVID-19 (PASC). The Company has provided BHC with an unrestricted investigational grant to conduct this study. BHC is a non-profit, interdisciplinary Center of Excellence advancing the diagnosis and treatment of chronic fatigue disorders, FM, post-viral syndromes, and related comorbidities.
For more information, please visit www.virios.com