Scientific Advisory Board
 
David Sabatini, MD, PhD
Co-founder and Chairman of the Scientific Advisory Board of Navitor, Professor of Biology, MIT; Member, Whitehead Institute; HHMI Investigator

David Sabatini is a Member of the Whitehead Institute for Biomedical Research, Senior Associate Member at the Broad Institute of MIT and Harvard and Member of the Koch Institute for Integrative Cancer Research at MIT, and Professor of Biology at MIT. He is also an Investigator of the Howard Hughes Medical Institute.

 
Michael N. Hall, PhD
Professor, Vice-Director and former Chair of Biochemistry, Biozentrum of the University of Basel

Michael Hall joined the Biozentrum of the University of Basel (Switzerland) in 1987 where he is currently Professor and former Chair of Biochemistry. Dr. Hall is a pioneer in the fields of TOR signaling and cell growth. He discovered the highly conserved, nutrient-activated protein kinase TOR (Target of Rapamycin) in the early 1990’s, and subsequently elucidated its role as a central controller of cell growth.

His subsequent studies include the discovery of the two structurally and functionally distinct TOR complexes (TORC1 and TORC2) and the description of the two signaling branches mediated by these two complexes. More recently, he demonstrated that mammalian TOR (mTOR) signaling in metabolic organs controls whole body growth and metabolism. As a central controller of growth and metabolism, TOR plays a key role in development and aging, and is implicated in disorders such as cancer, cardiovascular disease, diabetes, and obesity.

Dr. Hall is a member of the US National Academy of Sciences, has received numerous awards, including the Louis-Jeantet Prize for Medicine (2009), the Marcel Benoist Prize for Sciences or Humanities (2012), the Breakthrough Prize in Life Sciences (2014), the Canada Gairdner International Award (2015), and the Albert Lasker Award for Basic Medical Research (2017).  He has served on several editorial and scientific advisory boards. He received his PhD from Harvard University and was a postdoctoral fellow at the Pasteur Institute (Paris, France) and the University of California, San Francisco.

 
Brian Hubbard, PhD
Partner, Sprout BioVentures

Dr. Hubbard brings extensive knowledge of drug discovery and development with over 20 years of experience in the biopharmaceutical industry.  Before cofounding Sprout, Dr. Hubbard built an industry-facing group at the Broad Institute serving as Director of Therapeutics Projects, Center for the Science of Therapeutics. Prior to the Broad, he was Senior Director of Cardiovascular Diseases at Merck, where he was responsible for strategy and execution of research. His focus was primarily atherosclerosis research. While at Merck, Dr. Hubbard was also part of a core team that developed a strategic plan for restructuring basic research in the pharmaceutical industry. Prior to his work at Merck, Dr. Hubbard was Director of Cardiovascular and Metabolism Research at Novartis Institutes for Biomedical Research and did research into metabolic diseases and obesity at Millennium Pharmaceuticals.

Dr. Hubbard received his BS in chemistry from The College of William and Mary and a PhD in chemistry from the University of Illinois Champaign-Urbana. He did postdoctoral research in biochemistry and antibiotics at Harvard Medical School.

 
Brendan Manning, PhD
Professor of Genetics and Complex Diseases, Harvard School of Public Health

Brendan Manning’s research is focused on the interface between signaling and metabolic control under physiological and pathophysiological conditions. He is particularly interested in defining the control mechanisms and functions of a complex signaling network that is implicated in a diverse array of human diseases, including the majority of genetic tumor syndromes and cancers; metabolic diseases, such as diabetes and cardiovascular disease; neurocognitive and neurodegenerative diseases, such as autism and Alzheimer’s and autoimmune diseases.

As a postdoctoral fellow in the laboratory of Lewis Cantley, Dr. Manning found that the tumor suppressor TSC2 is the key molecular link between the PI3K and mTOR pathways. This finding helped connect a primary growth factor and insulin-stimulated pathway (PI3K), which is also activated in the majority of cancers, to a ubiquitous nutrient-sensing protein kinase that promotes cell growth (mTOR). Since that early landmark discovery, he has continued to make major contributions to our understanding of this key regulatory hub in mammalian cells and tissues, including the recognition that mTOR is a central player in the control of anabolic processes driving the synthesis of proteins, nucleic acids and lipids. His laboratory’s findings are providing both underlying mechanisms and potential therapeutic strategies for common complex diseases, such as cancer and diabetes. In the future, Dr. Manning plans to expand his research to explore molecular events contributing to aging and autism spectrum disorders, other areas where this signaling network has been implicated.

Dr. Manning received his PhD in molecular, cellular, and developmental biology from Yale University in 2000. After completing his postdoctoral training in signal transduction, cell biology, and systems biology at Harvard Medical School, he was recruited to Harvard School of Public Health in 2004, as the first junior faculty member of the then newly established Department of Genetics and Complex Diseases. Dr. Manning is also affiliated with the research programs in cancer cell biology and kidney cancer at Dana Farber/Harvard Cancer Center.  He is a recipient of the prestigious National Cancer Institute Outstanding Investigator Award (2015).

 
Mark Murcko, Ph.D.
Principal, Disruptive Biomedical, LLC

Mark Murcko has directly contributed to 5 marketed drugs and several others currently in mid to late-stage clinical trials. Dr. Murcko is currently the Principal at Disruptive Biomedical, LLC, an independent consultant and is a Professor of Practice at MIT and SVP, Strategy for Schrödinger, a leading software provider for drug discovery and materials science applications. Dr. Murcko also currently serves on numerous scientific advisory boards and corporate boards of directors for a diverse range of companies in the biomedical space.

Until November 2011 Dr. Murcko was Chief Technology Officer and Chair of the Scientific Advisory Board of Vertex Pharmaceuticals. In this role, he was responsible for the identification, validation, and incorporation of disruptive technologies across global R&D. Dr. Murcko is a co-inventor of the HCV protease inhibitor Incivek™ (telaprevir), as well as Agenerase™ (amprenavir) and Lexiva™ (fosamprenavir), Vertex’s two marketed drugs for HIV. In addition, he guided the early efforts of the Vertex’s cystic fibrosis program that produced the marketed drug Kalydeco™ (ivacaftor) and several other CF compounds currently in late-stage development. Dr. Murcko is also a co-inventor of 8 other clinical candidates in the areas of cancer, inflammation/immunology, and infectious disease and was responsible for starting many of Vertex’s programs in these and other disease areas, notably Vertex’s influenza drug VX-787 currently in phase II. Prior to Vertex, Dr. Murcko worked at Merck Sharpe & Dohme, where he helped discover clinical candidates against infection and cardiovascular and ocular diseases, including inhibitors of the enzyme carbonic anhydrase for the treatment of glaucoma. One of Merck’s development candidates in this area, Trusopt™ (dorzolamide), became the first marketed drug in pharmaceutical history to result from a structure-based drug design program.

Dr. Murcko has served on the editorial boards of many scientific publications, was the co-organizer of the 2008 ACS National Medicinal Chemistry Symposium, and served as the Chair of the 2013 Gordon Research Conference in Medicinal Chemistry. He is a co-inventor on more than 50 issued and pending patents, has co-authored more than 85 scientific articles, and has delivered more than 180 invited lectures. He received his Ph.D. in physical organic chemistry from Yale University.

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