Treating non-small cell lung tumors with a novel inhaled dry powder chemotherapeutic formulation
Project Number5R44CA277898-02
Former Number1R44CA277898-01
Contact PI/Project LeaderBEVERLIN II, BRYCE
Awardee OrganizationQUENCH MEDICAL, INC.
Description
Abstract Text
Project Summary / Abstract
Significance
Lung cancer is the leading cause of cancer mortality with a 5-year survival rate of less than 20% following
standard of care therapy.
Problem
Despite the use of aggressive surgery, combination chemotherapy and immunotherapy, a major limitation in the
control of primary and metastatic non-small cell pulmonary tumors with the use of the systemic administration of
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 be 1) scale-up the lead Quench EEG formulation and conduct characterization, stability,
and performance studies, and 2) conduct IND-enabling toxicology studies in an established inhalation toxicology
rodent model for regulatory submission.
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.
Public Health Relevance Statement
Project Narrative
Lung cancer is the leading cause of cancer mortality with a 5-year survival rate of less than 20% following
standard of care treatment. 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.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAerosolsBlood VolumeBypassCancer EtiologyCancer PatientCellsCharacteristicsCirculationClinicalClinical ResearchCombination Drug TherapyDataDepositionDoseDrug Delivery SystemsDrynessEffectivenessElectroencephalographyElementsEquipment ContaminationExcipientsFormulationGrowthHistologicHumanImmunotherapyIn VitroInhalationInhalation ToxicologyInhalatorsIntravenousInvestigational DrugsInvestigational New Drug ApplicationLeadLeucineLungLung NeoplasmsMalignant neoplasm of lungMaximum Tolerated DoseMedicalMedical StaffMedicineMetabolismMethodsNational Heart, Lung, and Blood InstituteNebulizerNon-Small-Cell Lung CarcinomaOncologyOperative Surgical ProceduresOral cavityOutcomePathway interactionsPatientsPenetrationPerformancePeripheralPharmaceutical PreparationsPharmacotherapyPharyngeal structurePhasePowder dose formProductionResearchRiskRodentRodent ModelRouteSafetySmall Business Innovation Research GrantSodium ChlorideSurvival RateTechniquesTechnologyTestingTherapeuticToxicokineticsToxicologyTranslationsTreatment outcomeTumor BurdenTumor TissueUnited States Food and Drug AdministrationUnited States National Institutes of HealthUniversitiesVirginiaWettabilityWorkchemotherapycommercializationdrug developmentefficacy studyfirst-in-humangemcitabinegood laboratory practiceimprovedin vivoinnovationmanufacturemetermortalitynovelparticlepre-clinicalpreclinical studyscale upside effectstandard of caresystemic toxicitytargeted deliverytranslational potentialtumor
No Sub Projects information available for 5R44CA277898-02
Publications
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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