DiagnosticsNature Reviews: Drug Discovery Article Describes Design Of Glycomimetic Compounds And Newly "Druggable" Disease Targets
GlycoMimetics, Inc. announced the publication of an article in Nature Reviews: Drug Discovery describing how novel small molecule compounds that mimic carbohydrates can be successfully designed and optimized to treat cancer, inflammatory disorders and other diseases.
Carbohydrates play essential roles in human biology and disease processes, but have been a relatively untapped for new drugs due to poor pharmaceutical properties of the naturally occurring molecules. The article published in Nature Reviews: Drug Discovery describes how researchers have successfully taken a distinct approach to developing new agents, known as glycomimetics. These novel compounds mimic carbohydrates and are capable of targeting disease-related carbohydrate-mediated functions. GlycoMimetics, Inc. has been applying its advanced understanding of carbohydrate chemistry to the development of a pipeline of promising glycomimetic product candidates, including GMI-1070, a pan-selectin inhibitor.
The article, "From Carbohydrate Leads to Glycomimetic Drugs," appears on July 24, 2009 in the advance online publication and in the August 1, 2009 print edition of Nature Reviews: Drug Discovery and is co-authored by John L. Magnani, Ph.D., Chief Scientific Officer of GlycoMimetics, Inc. and Beat Ernst, Ph.D., Professor of Molecular Pharmacy at the University of Basel, Switzerland.
"Carbohydrates play vital roles in many diseases, and act as key recognition molecules in both normal and pathological conditions," said Dr. Magnani. "The entire field has been achieving important advances in understanding exactly how carbohydrates function. These advances present opportunities for the rational design of new small-molecule drugs with desirable pharmacological properties that address a broad range of therapeutic targets for serious diseases."
GMI-1070 is an example of a rationally designed glycomimetic inhibitor whose structure is presented in the review. It is an antagonist of E-, P- and L-selectins, and inhibits a key early step in the inflammatory process leading to leukocyte adhesion and recruitment to inflamed tissue. In preclinical studies, GMI-1070 restored blood flow to affected vessels of sickle cell animals experiencing vaso-occlusive crisis by mediating the acute adhesion and aggregation of leukocytes and erythrocytes. GMI-1070 has completed Phase 1 clinical trials, and planning is underway for a Phase 2 study in sickle cell patients undergoing vaso-occlusive crisis. In Phase 1 studies, GMI-1070 was well tolerated and demonstrated drug-like properties in pharmacokinetic and metabolic evaluations.
"GMI-1070 is just the first of several rationally designed carbohydrate mimics in a pipeline of drug candidates based on our platform chemistry," said Rachel King, CEO of GlycoMimetics, Inc. "The data from the clinic has been encouraging, and we"re very excited about the potential of GMI-1070 in treating sickle cell patients, as well as therapeutic applications for the entire class of these new agents."
About Sickle Cell Disease and Vaso-Occlusive Crisis
Vaso-occlusive crisis is the main clinical feature of sickle cell disease, often resulting in significant clinical complications, and sometimes death. Currently, there are no mechanism-based therapies for treatment of vaso-occlusive crisis. Treatment consists primarily of supportive therapy in the form of hydration and pain control, typically requiring hospitalization for five to six days. There are more than 75,000 hospitalizations per year associated with vaso-occlusive crisis in the U.S.
GlycoMimetics, Inc.