Chronic and inflammatory pain affect millions and new treatments are urgently needed. Despite significant investment in opioid safety and formulation, there is little exploration of drugs with fundamentally novel mechanisms of action. Our goal is to develop such medicines based on novel protein therapeutics that block pain sensation by silencing multiple NaV sodium channels in nociceptors. The failure of NaV1.7 inhibitors as analgesics1 suggests that blocking more than one channel will be necessary. We will therefore take an approach involving a multivalent scaffold and small proteins that inhibit several NaV channels with tunable selectivity and potency. Activity will be measured by differential screening against human iPSC-derived sensory, cortical, and motor neurons. Over a two year period we expect to achieve hit/lead generation for 10-30 distinct molecules and optimization of the most active for testing in animals.

Funding

Funding level

Development

People

Principal Investigator

Pamela Silver

PhD
Elliott T. and Onie H. Adams Professor of Biochemistry and Systems Biology, Harvard Medical School
Co-PI

Bruce Bean

PhD
Robert Winthrop Professor of Neurobiology, Harvard Medical School

Peter Sorger

PhD
Otto Krayer Professor of Systems Pharmacology, Harvard Medical School

Clifford Woolf

PhD, MB, BCh
Professor of Neurology, Boston Children's Hospital

Follow on Funding and Exits

Federal/Foundations Funding

Federal/Foundations Funding