Non-clinical Development of a Synthetic Lung Surfactant for Treatment of NRDS
Non-clinical Development of a Synthetic Lung Surfactant for Treatment of NRDS
批准号:
10252528
负责人:
Gary Fujii
金额:
$95.69万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-06-18 至 2023-05-31
关键词:
37 weeks gestationAdvanced DevelopmentAnimalsApplications GrantsBiological AssayBronchopulmonary DysplasiaBusinessesCase StudyCause of DeathCessation of lifeChemical SurfactantsChildClinicalClinical ProtocolsClinical ResearchClinical TrialsCyclic GMPDevelopmentEquipmentFDA approvedFacility ConstructionGuidelinesHumanHuman ResourcesIncidenceInfantInvestigationLifeLipidsLive BirthMethodsMolecularMorbidity - disease rateNeonatal Respiratory DistressNosocomial InfectionsOryctolagus cuniculusPerformancePharmaceutical PreparationsPharmacologic SubstancePhasePhase I Clinical TrialsPhase II Clinical TrialsPregnancyPremature BirthPremature InfantProceduresProteinsPublic HealthPulmonary Surfactant-Associated Protein BPulmonary SurfactantsQualifyingQuality ControlResearchRiskSafetySalesScheduleSecureSmall Business Innovation Research GrantSourceSystemTrainingTranslatinganalytical methodbasecostcost effectiveimprovedinfant morbidity/mortalityintraventricular hemorrhagelow and middle-income countriesmanufacturing processmeetingsmortalityneonatepeptide Bpeptidomimeticspre-clinicalpreclinical developmentprematurepreterm newbornpublic health relevancerespiratorysurfactantsurfactant deficiency
中文摘要
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英文摘要
Project Summary/Abstract
Surfactant deficiency in preterm infants causes the neonatal respiratory distress syndrome (NRDS). NRDS
directly causes mortality and morbidity. NRDS also increases the risk of intraventricular hemorrhage,
bronchopulmonary dysplasia, and nosocomial infections. The burden of NRDS has been conservatively
estimated at 1% of all live births, or 1.4 million neonates globally, with a reported case fatality for untreated NRDS
of 57 to 89% in low- and middle-income countries. Although animal-derived surfactants for treating NRDS
developed in the 1980s greatly decreased preterm infant morbidity and mortality, fewer than one-third of
premature infants receive surfactant treatment (based on surfactant sales). Cost constraints and lack of supply
are primary factors for why the remaining two-thirds are not treated. To help fill this need, Molecular Express,
Inc. proposes to complete the late stage development and preclinical activities for ME-101, an investigational
lung surfactant comprised of the Super Mini-B peptide, which mimics Surfactant Protein B, the protein component
primarily responsible for lung surfactant activity, as well as the three-major lipids of natural human lung
surfactant. ME-101 is a fully synthetic lung surfactant - i.e., it is not limited by supply as is the case with animal
derived products and has significant advantages in being well-defined with consistent activity, product uniformity,
and economy of manufacturing over currently marketed animal and synthetic lung surfactants. The primary Aims
of this Direct-to-Phase II SBIR application are to establish a commercially viable process for manufacturing and
quality control of ME-101, implement a quality management system, produce and release a cGMP lot of ME-
101, perform IND enabling activities, and organize, schedule and conduct a Pre-IND meeting with the FDA to
gain final alignment on the clinical studies to demonstrate safety, tolerability, and efficacy. Successful execution
of these Aims will advance the development of a synthetic lung surfactant with commercial attractiveness due to
advantages over other synthetic surfactants in activity and manufacturing economy. Reduced cost to consumers
can potentially translate into broadened surfactant treatment of NRDS and potentially other indications for use
thus exerting a significant impact on improving global public health.
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