Kaleido Biosciences Initiates Controlled Clinical Study with Massachusetts General Hospital of Microbiome Metabolic Therapy KB109 in Outpatients with Mild-to-Moderate COVID-19
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Kaleido Biosciences Initiates Controlled Clinical Study with Massachusetts General Hospital of Microbiome Metabolic Therapy KB109 in Outpatients with Mild-to-Moderate COVID-19

- Second Study Launched in Kaleido’s COVID-19 Clinical Development Program for this Rapidly Growing Patient Population -

LEXINGTON, Mass., July 23, 2020 (GLOBE NEWSWIRE) -- Kaleido Biosciences, Inc. (Nasdaq: KLDO), a clinical-stage healthcare company with a chemistry-driven approach to targeting the microbiome to treat disease and improve human health, today announced the initiation of a controlled clinical study (K032) being conducted with Massachusetts General Hospital, evaluating Microbiome Metabolic Therapy (MMT) candidate KB109 added to Supportive Self-Care (SSC) for outpatients with mild-to-moderate COVID-19. This is the second clinical study Kaleido has initiated in this patient population, which, according to the World Health Organization, comprises approximately 80% of those experiencing symptoms.

“Massachusetts General Hospital is an ideal partner to conduct this important clinical study, building on the previously initiated study and adding to the scientific rationale for the role of the microbiome in the immune response to respiratory viral infections,” said Katharine Knobil, M.D., Kaleido’s Chief Medical Officer and Head of Research & Development. “As the spread of the virus continues, further study is needed in patients with mild-to-moderate disease to understand how to prevent progression to more severe sequelae. The evidence supporting the role of the microbiome in viral infections is compelling, and our clinical program will evaluate the effects of KB109 in mitigating inappropriate inflammatory response to COVID-19, and potentially avoiding more serious complications.”

“This study has the potential to inform us about how targeting the microbiome may help modulate the immune pathology associated with COVID-19 in the largest segment of infected patients, where there is still a significant need and opportunity,” said Michael Dougan, M.D., Ph.D., of the Division of Gastroenterology, Massachusetts General Hospital and Assistant Professor, Harvard Medical School.

This non-IND clinical study (K032) aims to include approximately 50 COVID-19 positive outpatients with mild-to-moderate disease. Patients will be randomized (1:1) to either receive SSC (the control group) or SSC plus KB109 for two weeks, and then followed for three weeks. Patients will be evaluated for safety, physiologic effects, and gut microbiota structure and function.

Patients will monitor and record objective measures, such as temperature and oxygen levels, and participate in telemedicine visits with clinicians. The study will assess healthcare utilization, and biomarkers of the inflammatory response that will inform the potential of KB109 in COVID-19 as well as other viral and bacterial infections. The composition and metabolites of patients’ microbiomes will be evaluated to understand the link between changes in the microbiome and inflammatory response to COVID-19 infection.