R43CA250617
Project Grant
Overview
Grant Description
Treating non-small cell lung tumors with a novel inhaled dry powder chemotherapeutic formulation.
Awardee
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Minnesota
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 07/31/21 to 07/31/22.
Quench Medical was awarded
Project Grant R43CA250617
worth $400,000
from National Cancer Institute in August 2020 with work to be completed primarily in Minnesota United States.
The grant
has a duration of 2 years and
was awarded through assistance program 93.395 Cancer Treatment Research.
The Project Grant was awarded through grant opportunity PHS 2019-02 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 I
Title
Treating non-small cell lung tumors with a novel inhaled dry powder chemotherapeutic formulation
Abstract
Project Summary / Abstract Significance Lung cancer is the leading cause of cancer mortality with a 5-year survival rate of 16% following surgery and intravenous chemotherapy. Problem Despite the use of aggressive surgery and combination chemotherapy, a major limitation in the control of primary and metastatic non-small cell pulmonary tumors with the use of the systemic administration of chemotherapy drugs is the low drug concentration in the lungs due to blood volume dilution and metabolism. There is a critical unmet medical need to develop new strategies to improve patient treatment outcomes. Innovation In contrast to systemic delivery of chemotherapy, inhalation delivers a chemotherapeutic drug directly to tumor tissues in the lung thereby enhancing its efficacy and safety due to increased local drug concentration in the lung, decreased systemic drug levels in the circulation, and decreased systemic toxicity. Gap Preliminary pre-clinical in-vivo studies using nebulized chemotherapy drugs has demonstrated efficacy and established the feasibility of delivery via aerosol, but nebulization of toxic drugs has major drawbacks. These drawbacks include a lack of efficient peripheral airway penetration, high mouth-throat deposition, contamination of equipment, and collateral aerosol risk to medical staff. Project Objective To address these drawbacks, we are developing a new method of delivering a chemotherapeutic drug via inhalation to reach pulmonary tumors directly in order to maximize the effectiveness and safety of the aerosol treatment with a fraction of the standard dose. We will create a novel dry powder chemotherapeutic formulation containing an FDA approved chemotherapy medication for the treatment of non- small cell lung cancer. Aims Aims of this proposal will evaluate the feasibility of manufacturing the novel formulation and then demonstrating efficacy in an established in-vivo lung cancer model. Commercial Potential Translation of this technology into a clinically beneficial inhalable chemotherapy product has the potential to significantly improve the treatment of pulmonary tumors in lung cancer patients by delivering targeted lower doses of medicine directly to the lung while minimizing systemic toxicity.Project NarrativeLung cancer is the leading cause of cancer mortality with a 5-year survival rate following surgery and intravenous chemotherapy of 16%. There is strong evidence that targeted delivery of inhaled chemotherapy medication to the lung at a fraction of the current dose will have a major impact on increasing survival and reducing lung tumor burden in lung cancer patients with far less side effects than those associated with current systemic intravenous chemotherapy. Based on preliminary data, we will develop a novel inhaled chemotherapy treatment in order to directly target pulmonary tumors in order to improve survival in lung cancer patients.
Topic Code
102
Solicitation Number
PA19-272
Status
(Complete)
Last Modified 12/5/22
Period of Performance
8/14/20
Start Date
7/31/22
End Date
Funding Split
$400.0K
Federal Obligation
$0.0
Non-Federal Obligation
$400.0K
Total Obligated
Activity Timeline
Transaction History
Modifications to R43CA250617
Additional Detail
Award ID FAIN
R43CA250617
SAI Number
R43CA250617-3924088293
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NC00 NIH NATIONAL CANCER INSTITUTE
Funding Office
75NC00 NIH NATIONAL CANCER INSTITUTE
Awardee UEI
JVLSL7GNVK25
Awardee CAGE
7WTF2
Performance District
04
Senators
Amy Klobuchar
Tina Smith
Tina Smith
Representative
Betty McCollum
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Cancer Institute, National Institutes of Health, Health and Human Services (075-0849) | Health research and training | Grants, subsidies, and contributions (41.0) | $400,000 | 100% |
Modified: 12/5/22