Feinstein Institute researcher receives $3.6M in grants to study rare bleeding condition

HHT is a genetic condition which causes patients' blood vessels not to form properly.  Their blood vessels develop abnormal shunts or holes that bypass the capillaries and could result in severe bleeding. In most cases, bleeding in tissues and organs can be treated by a doctor who cauterizes or embolize the point of the bleed. These interventions treat HHT symptoms; they do not address the condition. Furthermore, in some organs, such as the liver, these procedures cannot be performed and often require a liver transplant if the bleeding cannot be stopped. Dr. Marambaud hopes to identify therapies specifically tailored to correct the molecular defects associated with HHT, an approach that could provide a solution to prevent or even reverse the formation of the abnormal vessels and the resulting bleeding.

"Currently there is no treatment for hereditary hemorrhagic telangiectasia other than trying to stop the bleeding," said Dr. Marambaud. "We're extremely grateful for the support from the DOD and the NIH to allow us to continue our search for a treatment for this highly debilitating disease."

In this multi-site DOD study, Dr. Marambaud, along with Feinstein Institute Associate Professor Lionel Blanc, PhD, will identify potential drug candidates from existing FDA-approved medications to help reduce the loss of blood vessel function associated with HHT. Dr. Marambaud's findings will then be tested in human clinical trials at Toronto University, which houses the largest HHT care center in North America. Other institutions involved in the study include the Barrow Neurological Institute, Duke University and Pittsburg University.  The DOD has placed a research focus on vascular pathologies, like HHT, that might affect military personnel. HHT, although relatively rare, can be highly debilitating and is expected to affect military personnel at the same prevalence as the general population.

As part of the NIH study, Dr. Marambaud and his team will work to better understand the genetic causes of HHT to identify new therapies. HHT mutations are mostly found in the ALK1 and ENG genes and lead to a loss of function in the signaling associated with these genes. Researchers will examine collections of FDA-approved drugs to identify molecules capable of activating ALK1 and ENG signaling. Drugs identified in this study can then be tested in humans in a clinical trial.

Kevin J. Tracey, MD, president & CEO of the Feinstein Institute said, "Dr. Marambaud's research to repurpose FDA-approved medications offers a more efficient path for new therapies that are desperately needed for this devastating illness."

About The Feinstein Institute
The Feinstein Institute for Medical Research is the research arm of Northwell Health, the largest healthcare provider in New York. Home to 50 research laboratories and to clinical research throughout dozens of hospitals and outpatient facilities, the 3,500 researchers and staff of the Feinstein Institute are making breakthroughs in molecular medicine, genetics, oncology, brain research, mental health, autoimmunity and bioelectronic medicine – a new field of science that has the potential to revolutionize medicine. For more information about how we empower imagination and pioneer discovery, visit FeinsteinInstitute.org.

Contact: Heather E. Ball
516-425-7917
[email protected]

SOURCE The Feinstein Institute for Medical Research

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