This conference provides an exclusive global partnering forum for senior executives, bankers, venture capitalists and business development professionals from prominent biotech and pharmaceutical companies. At this year’s conference, over 50 companies will have the opportunity to showcase their cutting-edge technologies for international partnerships. Immunis Inc is truly humbled to be one of them.
Dr. Keirstead is looking forward to sharing Immunis’ investigational secretome product, STEM, with leaders from the world’s top translational research institutions. STEM is all-natural, all-human and represents a perfectly balanced set of immune modulators at relevant, physiological concentrations. STEM is currently being tested in a Phase 1/2a clinical trial for safety and efficacy in elderly individuals with muscle atrophy associated with knee osteoarthritis.
About Global Life Science Partnering and Investor Conference
With over 650 one-on-one partnering meetings, the Global Life Science Partnering and Investor Conference is a premier event for emerging companies to seek funding and partnerships. For more information please visit: www.biocom.org/conferences/global-partnering-conference/
About Immunis Inc.
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
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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