Immunis Chairman Dr. Hans Keirstead to Present at NextMed Health
Immunis Chairman Dr. Hans Keirstead to Present at Abundance360
Dr. Greilach is thrilled to be part of a conference that serves as a bridge between academia and industry. The Festival of Biologics provides a one-of-a-kind platform to discuss Immunis’ investigational secretome product, STEM, which is currently being studied in several models of disease at multiple universities. Most importantly, Dr. Greilach will highlight Immunis’ Phase 1/2a clinical trial, where STEM is being investigated for safety and efficacy in patients with muscle atrophy. Dr. Greilach is looking forward to spreading his enthusiasm on the prospects of the stem cell secretome in biomedicine.
The vision of Festival of Biologics is to unite senior biologics professionals in a collaborative space to advance industry and improve human health. For more information please visit: https://www.terrapinn.com/conference/festival-of-biologics-usa/index.stm
Immunis is a private biotechnology company developing a novel immunomodulatory secretome product for the various manifestations of age and disease-related immune decline. The STEM product line leverages Immunis’ leading-edge capabilities in stem cell technologies to deliver a product of all natural, all human immune modulators in their natural relative physiological concentrations. For additional information about Immunis’ IMM01-STEM Phase 1/2a trial please visit: www.immunisbiomedical.com
About STEM-MYO
Immunis’ FDA-awarded Phase 1/2a clinical trial is an open-label dose escalation study to assess the safety and tolerability of IMM01-STEM in elderly participants with muscle atrophy associated with knee osteoarthritis. Up to 18 patients will be enrolled in the trial and randomly assigned to an IMM01-STEM dose cohort. Treatment will be administered in the form of intramuscular injections twice a week for four weeks (8 injections total). Male or female patients are eligible for the study if they satisfy the following criteria: (1) 50 to 75 years of age at the time of signing the informed consent, (2) have a grade 2 or 3 knee osteoarthritis as defined by Kellgren-Lawrence analyses, (3) have quadricep weakness (<7.5N/kg), (4) can ambulate >50 feet unassisted, (5) are negative for human immunodeficiency virus, hepatitis B surface antigen (HBsAg), and hepatitis C at the Screening Visit and (6) have a body mass index (BMI) of <40kg/m2. For additional information about Immunis’ trial participant qualifications, please visit: www.immunisbiomedical.com
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