Reversing Isoniazid Resistance By Isotopic Substitution
Reversing Isoniazid Resistance By Isotopic Substitution
批准号:
9347156
负责人:
GRAHAM S TIMMINS
金额:
$58.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-03-06 至 2019-02-28
关键词:
AddressAdverse effectsAffectBlindedBreath TestsCapital FinancingCell NucleusChemistryComplementContractsCouplingDataDeuteriumDevelopmentDrug KineticsDrug effect disorderDrug resistanceDrug resistance in tuberculosisFree RadicalsFundingFutureGoalsHumanHydrogenInvestigational DrugsIsoniazid resistanceIsotopesKineticsKnowledgeLabelLaboratoriesLegal patentLiteratureMagnetismMedicineMetabolismMultidrug-Resistant TuberculosisMutationMycobacterium tuberculosisPathway interactionsPharmaceutical PreparationsPharmacodynamicsPhasePhase I Clinical TrialsPositioning AttributePrivatizationProcessProtocols documentationPublic HealthReactionResistanceRifampinRiskRunningScienceScientistSilkSiteSmall Business Innovation Research GrantStable Isotope LabelingSystemTechnology TransferTestingToxic effectToxicologyTreatment CostTuberculosisWorkactive controldrug discoverygood laboratory practiceimprovedin vivoisoniazidmagnetic fieldmanufacturing processmutantnovelnovel strategiesnovel therapeuticspre-clinicalresearch clinical testingresistance mechanismresistant strainscale upstable isotopetheoriestuberculosis drugs
中文摘要
项目摘要
这个项目的总体目标是开发我们的新的稳定同位素标记的,版本的一个
现有的结核病(TB)药物异烟肼(INH)用于治疗耐药结核病。我们
假设我们同位素增强的化合物可以发展成一种强大的新的
通过解决以下具体问题,开发针对INH耐药结核病和多药耐药结核病的药物
目的:
具体目标1。确定其他INH耐药相关突变[酰基-13 C]INH可以
克服,并确定为什么[酰基-13 C]INH克服高INH的机制
突变体S315 T KatG菌株的抗性。
具体目标2。开发我们化合物的优化合成和技术转让
外部良好生产工艺的方案(TTP),符合GMP的生产。
具体目标3。收集非药物非临床研究质量管理规范(GLP)毒理学数据
化合物,以支持后续的GLP研究性新药(IND)使能研究。
顺利完成这些任务,将为风险投资资金和转移铺平道路
进行临床试验
英文摘要
Project Summary
The overall goal of this project is to develop our new stable isotope labeled, version of an
existing tuberculosis (TB) drug, isoniazid (INH) for use in treated drug resistant TB. We
hypothesize that our that isotope-enhanced compound can be developed into a powerful new
drug against INH-resistant TB and multidrug resistant-TB, by addressing the following specific
aims:
Specific Aim 1. Determine what other INH resistance-associated mutations [acyl-13C]INH can
overcome, and determine the mechanism for why [acyl-13C]INH overcomes the high INH
resistance of mutant S315T KatG strains.
Specific Aim 2. Develop an optimized synthesis of our compound and a Technology Transfer
Protocol (TTP) for external good manufacturing processes, GMP-capable manufacture.
Specific Aim 3. Collect non-Good Laboratory Practices (GLP) toxicology data on our
compound to support subsequent GLP Investigational New Drug (IND) enabling studies.
Successful completion of these tasks will pave the way for venture capital funding and transfer
of our compound into clinical testing.
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依托单位:--
海外基金