R44HL147776
Project Grant
Overview
Grant Description
Development of NAV1.7 selective inhibitors for the treatment of chronic cough - Project Summary
Chronic cough, or cough that persists for more than eight weeks, is a condition that is often associated with diseases such as chronic obstructive pulmonary disorder (COPD), asthma, idiopathic pulmonary fibrosis, bronchiectasis or gastroesophageal reflux disease (GERD). In other cases, the etiology is unknown, although it has been noted that the cough often first arises following a severe viral respiratory infection.
Chronic cough has significant physical, psychological, social, and economic consequences that negatively impact quality of life. Prevalence in the United States is as high as 11%, and in a majority of cases, the condition is refractory.
Compelling evidence supports the hypothesis that chronic cough arises from alterations in sensory physiology that cause hypersensitivity to previously innocuous stimuli. The voltage-gated sodium ion channel NAV1.7 is highly expressed in unmyelinated vagal nerve afferents that trigger cough through a sensorimotor reflex circuit.
Results from a published pre-clinical report show that reducing expression of NAV1.7 nearly abolishes cough evoked by inhaled irritants, indicating that it is a promising target for reducing cough.
SiteOne Therapeutics has discovered potent and selective small molecule inhibitors of NAV1.7 that block vagal C fiber activity in a dose-dependent manner.
During a Phase 1 program, our team demonstrated that systemic administration of an isoform-selective NAV1.7 inhibitor abolishes the cough response to inhaled irritants in conscious guinea pigs.
The objective of our Phase 2 program is to evaluate safety, pharmacokinetic, and efficacy endpoints, and to advance an inhaled NAV1.7 inhibitor into IND-enabling development as a therapeutic for chronic cough.
Chronic cough, or cough that persists for more than eight weeks, is a condition that is often associated with diseases such as chronic obstructive pulmonary disorder (COPD), asthma, idiopathic pulmonary fibrosis, bronchiectasis or gastroesophageal reflux disease (GERD). In other cases, the etiology is unknown, although it has been noted that the cough often first arises following a severe viral respiratory infection.
Chronic cough has significant physical, psychological, social, and economic consequences that negatively impact quality of life. Prevalence in the United States is as high as 11%, and in a majority of cases, the condition is refractory.
Compelling evidence supports the hypothesis that chronic cough arises from alterations in sensory physiology that cause hypersensitivity to previously innocuous stimuli. The voltage-gated sodium ion channel NAV1.7 is highly expressed in unmyelinated vagal nerve afferents that trigger cough through a sensorimotor reflex circuit.
Results from a published pre-clinical report show that reducing expression of NAV1.7 nearly abolishes cough evoked by inhaled irritants, indicating that it is a promising target for reducing cough.
SiteOne Therapeutics has discovered potent and selective small molecule inhibitors of NAV1.7 that block vagal C fiber activity in a dose-dependent manner.
During a Phase 1 program, our team demonstrated that systemic administration of an isoform-selective NAV1.7 inhibitor abolishes the cough response to inhaled irritants in conscious guinea pigs.
The objective of our Phase 2 program is to evaluate safety, pharmacokinetic, and efficacy endpoints, and to advance an inhaled NAV1.7 inhibitor into IND-enabling development as a therapeutic for chronic cough.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Bozeman,
Montana
597152438
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 04/30/23 to 04/30/24 and the total obligations have increased 78% from $677,568 to $1,204,605.
Siteone Therapeutics was awarded
Project Grant R44HL147776
worth $1,204,605
from National Heart Lung and Blood Institute in May 2019 with work to be completed primarily in Bozeman Montana United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity PHS 2020-2 Omnibus Solicitation of the NIH, CDC and FDA for Small Business Innovation Research Grant Applications (Parent SBIR [R43/R44] Clinical Trial Not Allowed).
SBIR Details
Research Type
SBIR Phase II
Title
Development of Nav1.7 Selective Inhibitors for the Treatment of Chronic Cough
Abstract
PROJECT SUMMARYChronic cough, or cough that persists for more than eight weeks, is a condition that is often associated with diseases such as chronic obstructive pulmonary disorder (COPD), asthma, idiopathic pulmonary fibrosis, bronchiectasis or gastroesophageal reflux disease (GERD). In other cases, the etiology is unknown, although it has been noted that the cough often first arises following a severe viral respiratory infection. Chronic cough has significant physical, psychological, social and economic consequences that negatively impact quality of life. Prevalence in the United States is as high as 11%, and in a majority of cases the condition is refractory.Compelling evidence supports the hypothesis that chronic cough arises from alterations in sensory physiology that cause hypersensitivity to previously innocuous stimuli. The voltage-gated sodium ion channel NaV1.7 is highly expressed in unmyelinated vagal nerve afferents that trigger cough through a sensorimotor reflex circuit. Results from a published pre-clinical report show that reducing expression of NaV1.7 nearly abolishes cough evoked by inhaled irritants, indicating that it is a promising target for reducing cough. SiteOne Therapeutics has discovered potent and selective small molecule inhibitors of NaV1.7 that block vagal C fiber activity in a dose-dependent manner. During a Phase 1 program, our team demonstrated that systemic administration of an isoform-selective NaV1.7 inhibitor abolishes the cough response to inhaled irritants in conscious guinea pigs. The objective of our Phase 2 program is evaluate safety, pharmacokinetic and efficacy endpoints, and to advance an inhaled NaV1.7 inhibitor into IND-enabling development as a therapeutic for chronic cough.PROJECT NARRATIVE Chronic cough is a debilitating medical condition that afflicts ~11% of the population in the United States and is not effectively treated with existing drugs. We aim to develop a safe and effective, inhaled antitussive product to reduce neurologic hypersensitivity in the lungs that is responsible for chronic cough. Such a therapeutic could also find use in the treatment of acute and subacute cough following viral infection with coronavirus, influenza or rhinovirus.
Topic Code
NHLBI
Solicitation Number
PA20-260
Status
(Complete)
Last Modified 9/20/24
Period of Performance
5/1/19
Start Date
4/30/24
End Date
Funding Split
$1.2M
Federal Obligation
$0.0
Non-Federal Obligation
$1.2M
Total Obligated
Activity Timeline
Transaction History
Modifications to R44HL147776
Additional Detail
Award ID FAIN
R44HL147776
SAI Number
R44HL147776-697136705
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NH00 NIH NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Funding Office
75NH00 NIH NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
Awardee UEI
ZKBYHMUQS291
Awardee CAGE
61AQ1
Performance District
MT-01
Senators
Jon Tester
Steve Daines
Steve Daines
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Heart, Lung, and Blood Institute, National Institutes of Health, Health and Human Services (075-0872) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,055,826 | 100% |
Modified: 9/20/24