SBIR/STTR Research Award

Discovery of NaV1.7 Inhibitors for the Treatment of Pain

Award identifier 348868663dabd4a2b76ad017fd075a877452a1ffa07a88fa23bbef667558e37bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$688,083

Program and phase

SBIR · Phase I

Award year

2019

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
SITEONE THERAPEUTICS, INC.
Proposal award date
2019-05-01
Contract end date
2021-04-30
UEI
ZKBYHMUQS291
Solicitation number
PAR18-541
Topic code
105

Research abstract

PROJECT SUMMARY The objective of our program is to develop a safe and effective nonopioid analgesic for the treatment of neuropathic pain, such as pain associated with chemotherapy-induced peripheral neuropathy, that targets an isoform of the voltage-gated sodium ion channel, NaV1.7. Voltage-gated sodium channels are involved in the transmission of nociceptive signals from their site of origin in the peripheral terminals of DRG neurons to the synaptic terminals in the dorsal horn. Ten mammalian isoforms exist, NaV1.1–1.9 and NaX. NaV1.7 is the most abundant tetrodotoxin-sensitive sodium channel in small diameter myelinated and unmyelinated afferents, where it has been shown to modulate excitability and set the threshold for action potentials. Humans lacking functional NaV1.7 due to a rare genetic condition are unable to experience almost all types of pain. Efforts to develop systemic inhibitors of NaV1.7 have been complicated by the challenge of achieving selectivity over other NaV isoforms expressed in the diaphragm, phrenic nerve, heart and central nervous system that are critical for safety. SiteOne Therapeutics has discovered a series of potent, state-independent NaV1.7 inhibitors that exhibit andgt;1000-fold selectivity over other human isoforms. Work conducted under this program will support advancement of a lead candidate into clinical development as a therapeutic for neuropathic pain.PROJECT NARRATIVE Chemotherapy-induced peripheral neuropathy is a common side effect of drugs used for the treatment of cancer. Symptoms include severe pain and sensitivity that can last for months or years after the completion of treatment, and often lead to dose reductions or discontinuation. As a result, many patients receive suboptimal cancer therapy. Our program aims to develop an effective, nonopioid therapeutic for pain associated with chemotherapy-induced neuropathy with no potential for abuse or addition. If successful, the product could also find use in the treatment of other chronic severe pain conditions.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

10 SBIR/STTR records share this UEI (2013–2021). Reported award amounts total $8,523,209. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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