Englewood Cliffs NJ, July 12, 2021 — Silo Pharma, Inc. (OTCQB: SILO), a development stage biopharmaceutical company, today announced that it has entered into a Scientific Research Agreement with the University of Maryland, Baltimore.
The main objective of our study is to evaluate the pharmacokinetics of dexamethasone delivered to arthritic rats via liposomes. We have selected this drug because it represents one of the mainstream drugs for RA that is currently in use. The novelty of our approach lies in drug delivery via peptide-guided liposomes, which is aimed at enhancing the efficacy/toxicity profile of dexamethasone. By selecting a drug that is already approved by the FDA, we can focus on the drug delivery aspect of our technology for commercialization purposes. Our technology platform can also be adapted for use with other drugs because liposomes can be loaded with both hydrophobic and hydrophilic drugs, thus, permitting combination drug therapy.
Eric Weisblum, Chairman and CEO of Silo Pharma stated “This agreement is a milestone for the company as we add a significant addressable market for our therapeutic approach. This study will not only allow us to study the efficacy of the homing peptides but will help establish our hypothesis that we can not only target parts of the body but can lower toxicity and help keep healthy organs unexposed to therapeutics.”
About Silo Pharma
Silo Pharma is a development stage biopharmaceutical company focused on merging traditional therapeutics with psychedelic research for people suffering from indications such as depression, PTSD, Parkinson’s, and other rare neurological disorders. Silo’s mission is to identify assets to license and fund the research which we believe will be transformative to the well-being of patients and the health care industry. For more information, visit www.silopharma.com.
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