capricor therapeutics clinical trials

All forward-looking statements in this press release are based on information available to Capricor as of the date hereof, and Capricor assumes no obligation to update these forward-looking statements. Intraday data delayed at least 15 minutes or per exchange requirements. The study challenged the long-standing convention that cardiac scarring is permanent and healthy heart muscle cannot be restored. None of Capricor’s exosome-based candidates have been approved for clinical investigation. Multiple published peer-reviewed studies of CDCs have demonstrated favorable modulation of various inflammatory cytokines and regulation of the immune response. DYNAMIC Phase I. Malliaras et al. Capricor Therapeutics Announces U.S. FDA Acceptance of its IND Application for a Phase 2 Clinical Trial of CAP-1002 in Patients with COVID-19 Email Print … (C) Copyright 2020 GlobeNewswire, Inc. All rights reserved. Intraday Data provided by FACTSET and subject to terms of use. The current understanding of COVID-19's later stages are thought to be due to overstimulation of the immune system, which triggers a cytokine storm in which the body is overwhelmed with pro-inflammatory molecules. Cenderitide Phase II. There are a number of important factors that could cause actual results or events to differ materially from those indicated by such forward-looking statements. About Capricor Therapeutics Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a clinical-stage biotechnology company focused on the discovery, development and … Patient participation will be a maximum of 13 weeks from screening. CAP-1002 consists of allogeneic cardiosphere-derived cells, or CDCs, a type of cardiac cell therapy that has been shown in pre-clinical and clinical studies to exert potent immunomodulatory activity. For patients assigned to receive CDCs, autologous cells were grown from endomyocardial biopsy specimens received from the same patient and were then infused into the infarct-related artery 1.5-3 months after myocardial infarction. This randomized, double-blind, placebo-controlled trial will enroll subjects with a clinical diagnosis of COVID-19 confirmed by laboratory testing. The Dilated cardiomYopathy iNtervention with Allogeneic MyocardIally-regenerative Cells (DYNAMIC) Phase I trial evaluated CAP-1002 in patients with advanced heart failure. Cautionary Note Regarding Forward-Looking Statements. Is there a problem with this press release? The trial was conducted at Cedars-Sinai Medical Center and Johns Hopkins University and was sponsored by Cedars-Sinai Medical Center under the leadership of Eduardo Marbán, M.D., Ph.D., Director of the Cedars-Sinai Heart Institute and Co-Founder and Scientific Advisory Board Chairman of Capricor.

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