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IMAC Holdings, Inc. Announces Completion of Second Cohort of its Phase 1 Clinical Study of Umbilical Cord-Derived Mesenchymal Stem Cells for the Treatment of Bradykinesia Due to Parkinson’s Disease

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IMAC Holdings has successfully completed the second cohort of its Phase 1 clinical trial on umbilical cord-derived mesenchymal stem cells for treating bradykinesia in Parkinson’s patients. Five patients received medium concentration intravenous infusions, completed on February 15, 2022. Safety assessments will be ongoing for 30 days before the final cohort begins. The trial aims to ensure safety and tolerability for 15 participants across three dosage groups over a 12-month tracking period. This research supports IMAC's broader goal of innovative therapies for movement-restricting diseases.

Positive
  • Completion of second cohort in Phase 1 clinical trial indicates progress in research.
  • Potential market impact with a growing Parkinson's disease therapeutics market projected to reach $5.28 billion by 2025.
Negative
  • The trial's dependency on safety assessments could delay further progression to the final cohort.
  • Risks associated with the investigational nature of the compound may affect investor confidence.

BRENTWOOD, Tenn., Feb. 16, 2022 (GLOBE NEWSWIRE) -- IMAC Holdings, Inc. (Nasdaq: IMAC) (“IMAC” or “the Company”), today announces it has completed the second cohort of its Phase 1 clinical trial for its investigational compound utilizing umbilical cord-derived allogenic mesenchymal stem cells for the treatment of bradykinesia due to Parkinson’s disease.

The second cohort consists of five patients with bradykinesia due to Parkinson’s disease receiving an intravenous infusion of a medium concentration stem cell treatment. The cohort was completed on Tuesday, February 15, 2022. In accordance with the trial protocol, the Company will wait at least 30 days to demonstrate safety of the medium concentration dose before initiating the third and final cohort in which five patients will receive a high concentration intravenous dose of stem cells.

About IMAC’s Phase 1 Clinical Trial

The Phase 1 clinical trial, consisting of a 15-patient dose escalation safety and tolerability study, is being conducted at three of IMAC’s clinical centers in Chesterfield, Missouri, Paducah, Kentucky, and Brentwood, Tennessee. The trial is divided into three groups: 1) five patients with bradykinesia due to Parkinson’s disease will receive a low concentration dose, intravenous infusion of stem cells, 2) five will receive a medium concentration intravenous dose, 3) and five will receive a high concentration intravenous dose. All groups will be subsequently tracked for 12 months. IMAC’s medical doctors and physical therapists at the clinical sites have been trained to administer the treatment and manage the therapy. Ricardo Knight, M.D., M.B.A., who is medical director of the Mike Ditka IMAC Regeneration Center, is the trial’s principal investigator.

The Institute of Regenerative and Cellular Medicine serves as the trial’s independent investigational review board, while Regenerative Outcomes provides management of the study. Further details of the trial can be found at clinicaltrials.gov.

About Bradykinesia Due to Parkinson’s Disease

In addition to unusually slow movements and reflexes, bradykinesia may lead to limited ability to lift arms and legs, reduced facial expressions, rigid muscle tone, a shuffling walk, and difficulty with repetitive motion tasks, self-care, and daily activities. Parkinson’s disease is the typical culprit of bradykinesia, and as it progresses through its stages, a person’s ability to move and respond declines.

According to Zion Market Research, the global Parkinson’s disease therapeutics market was $2.61 billion in 2018 and is expected to grow to $5.28 billion by 2025. The Parkinson’s Disease Foundation estimates that nearly 10 million people are suffering from Parkinson’s disease, and almost 60,000 new cases are reported annually in the U.S.

About IMAC Holdings, Inc.

IMAC was created in March 2015 to expand on the footprint of the original IMAC Regeneration Center, which opened in Kentucky in August 2000. IMAC Regeneration Centers combine life-science advancements with traditional medical care for movement restricting diseases and conditions. IMAC owns or manages more than 15 outpatient clinics that provide regenerative, orthopedic and minimally invasive procedures and therapies. It has partnered with several active and former professional athletes including Ozzie Smith, David Price, Mike Ditka and Tony Delk. IMAC’s outpatient medical clinics emphasize treating sports and orthopedic injuries and movement-restricting diseases without surgery or opioids. More information about IMAC Holdings, Inc. is available at www.imacregeneration.com.

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Safe Harbor Statement

This press release contains forward-looking statements. These forward-looking statements, and terms such as “anticipate,” “expect,” “believe,” “may,” “will,” “should” or other comparable terms, are based largely on IMAC's expectations and are subject to a number of risks and uncertainties, certain of which are beyond IMAC's control. Actual results could differ materially from these forward-looking statements as a result of, among other factors, risks and uncertainties associated with its ability to raise additional funding, its ability to maintain and grow its business, variability of operating results, its ability to maintain and enhance its brand, its development and introduction of new products and services, the successful integration of acquired companies, technologies and assets, marketing and other business development initiatives, competition in the industry, general government regulation, economic conditions, dependence on key personnel, the ability to attract, hire and retain personnel who possess the skills and experience necessary to meet customers’ requirements, and its ability to protect its intellectual property. IMAC encourages you to review other factors that may affect its future results in its registration statement and in its other filings with the Securities and Exchange Commission. In light of these risks and uncertainties, there can be no assurance that the forward-looking information contained in this press release will in fact occur.

IMAC Press Contact:

Laura Fristoe

lfristoe@imacrc.com


FAQ

What are the results of the second cohort in IMAC Holdings' Phase 1 clinical trial?

The second cohort completed successfully with five patients receiving medium concentration stem cell treatment, with safety evaluations scheduled.

What is the next step after the second cohort in IMAC's clinical trial?

After a 30-day safety assessment, the company will initiate the third and final cohort with high concentration doses.

How many patients are involved in IMAC Holdings' Phase 1 clinical trial?

The Phase 1 trial involves a total of 15 patients across three dosage groups.

When was the second cohort of the clinical trial completed?

The second cohort was completed on February 15, 2022.

What condition is IMAC Holdings' clinical trial targeting?

The trial is targeting bradykinesia due to Parkinson's disease.

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