The ARDS Advisory Board consultants are:
Michael A. Matthay, MD, Professor of Medicine and Anesthesia at the University of California at San Francisco
(UCSF), a Senior Associate at the Cardiovascular Research Institute,
and Associate Director of the Critical Care Medicine at UCSF. Dr.
Matthay's basic research has focused on the pathogenesis and resolution
of the acute respiratory distress syndrome (ARDS), with an emphasis on
translational work and patient-based research, including clinical
trials. Dr. Matthay's recent research has focused on the biology and
potential clinical use of allogeneic bone marrow derived mesenchymal
stromal cells (MSCs) for ARDS. He is currently leading the "Mesenchymal
Stromal Cells For Acute Respiratory Distress Syndrome (STAT)," a United
States Department of Defense supported study of MSCs for ARDS.
Mitchell M. Levy, MD, Chief, Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, The Warren Alpert Medical School of Brown University, where he is Professor of Medicine. Dr. Levy also serves as Medical Director of the Medical ICU at Rhode Island Hospital. He has been an investigator on numerous pharmacologic and biologic trials intended to treat sepsis, cardiovascular and pulmonary pathology. He has expertise in trial design, clinical trial execution and trial management and is one of the three founding members of the Surviving Sepsis Campaign (SSC). Dr. Levy is Past-President of the Society of Critical Care Medicine (2009).
Lorraine B. Ware, MD, Professor of Medicine and Ralph and Lulu Owen Endowed Chair, Professor of Pathology, Microbiology and Immunology, Vanderbilt University; Director, Vanderbilt Medical Scholars Program. Dr. Lorraine Ware's comprehensive bench-to-bedside research program centers on the pathogenesis and treatment of sepsis and acute lung injury with a current focus on mechanisms of lung epithelial and endothelial oxidative injury by cell-free hemoglobin. Dr. Ware is also a lead investigator for the "Mesenchymal Stromal Cells For Acute Respiratory Distress Syndrome (STAT)" study.
"We are extremely pleased to have been able to attract such a prestigious group of experts to advise and guide us in the Company's planned development of iMSC's for the treatment of ARDS" said Mr. Myron Holubiak, CEO of Citius. "These individuals are recognized opinion leaders and expert in the planning and execution of clinical trials in this therapeutic area. We will be seeking their advice in all phases of our clinical trial design."
About Citius Pharmaceuticals, Inc.
Citius is a
late-stage specialty pharmaceutical company dedicated to the development
and commercialization of critical care products, with a focus on
anti-infectives and cancer care. For more information, please visit www.citiuspharma.com.
About Citius iMSC
Citius's planned induced mesenchymal stem cell (iMSC) product is derived from a human induced pluripotent stem cell (iPSC)
line generated using a proprietary non-immunogenic and non-viral
mRNA-based (non-viral) reprogramming process. Unlike the MSCs derived
from bone marrow, placenta, umbilical cord, or adipose tissue these
proprietary iMSCs are based on a clonal process and therefore are
genetically homogeneous and exhibit superior potency and higher cell
viability. The Citius iMSC is an allogeneic (unrelated donor) mesenchymal stem-cell product manufactured by expanding material from an iMSC master cell bank. The master cell bank produces "off-the-shelf" iMSCs
that are uniform as compared to MSCs using donor-sourced cells, which
is subject to batch-to-batch and cell-to-cell variability that can
affect clinical safety and efficacy. In vitro studies demonstrate that iMSCs
are shown to secrete higher levels of immunomodulatory proteins than
donor-derived cells, and may reduce or prevent pulmonary injury
associated with acute respiratory distress syndrome (ARDS) in patients
with COVID-19.
About Acute Respiratory Distress Syndrome (ARDS)
ARDS
is a type of respiratory failure characterized by rapid onset of
widespread inflammation in the lungs. ARDS is a rapidly progressive
disease that occurs in critically ill patients – most notably now in
those diagnosed with COVID-19. ARDS affects approximately 200,000
patients per year in the U.S., exclusive of the current COVID-19
pandemic, and has a 30% to 50% mortality rate. ARDS is sometimes
initially diagnosed as pneumonia or pulmonary edema (fluid in the lungs
from heart disease). Symptoms of ARDS include shortness of breath, rapid
breathing and heart rate, chest pain (particularly while inhaling), and
bluish skin coloration. Among those who survive ARDS, a decreased
quality of life is relatively common.
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