Development of novel agents for the treatment of renal fibrosis
Development of novel agents for the treatment of renal fibrosis
批准号:
8780197
负责人:
ANIL K KARIHALOO
金额:
$61.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-01 至 2016-08-31
关键词:
AchievementAcuteAnimal ModelAreaBackBehaviorBiological AssayCYP2D6 geneCYP3A4 geneCaco-2 CellsCanis familiarisCell modelCharacteristicsChronic Kidney FailureClinicalDevelopmentDiabetic NephropathyDisease modelDoseDrug KineticsEnd stage renal failureEvaluationFeasibility StudiesFibrosisGoalsGrantHumanIn VitroInhibitory Concentration 50KidneyLeadLettersLiver MicrosomesLysophosphatidic Acid ReceptorsMedicalMetabolicModelingMusOral AdministrationPermeabilityPharmaceutical PreparationsPharmacotherapyPhasePositioning AttributePreparationPropertyRattusRenal Replacement TherapyResearchSafetySelection CriteriaSeriesSignal PathwaySmall Business Innovation Research GrantStreptozocinTestingTherapeutic InterventionToxic effectUreteral obstructionanalogclinical efficacycommercializationimprovedin vivolead serieslipophilicitymeetingsmortalitynovelnovel therapeuticspre-clinicalpreclinical studypreventprogramspublic health relevancesafety studyscale upsmall moleculestandard of caretherapy development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The ultimate goal of our project is to develop novel therapeutics effective in chronic kidney diseases that normally develop fibrosis, lead to end stage renal disease and require renal replacement therapy. This SBIR phase 2 application builds on the results obtained in phase 1 where novel and selective small molecule antagonists were discovered that prevent the progression of renal fibrosis in a unilateral ureteral obstruction
(UUO) animal model. Leads identified in phase 1 will be optimized for drug-like and ADME properties. Candidate compounds meeting the selection criteria will be assessed for safety in vivo and the best compound will be examined in several different animal models of chronic kidney disease to delineate a development path in the clinical setting.
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会议论文
Selective LPA1 receptor antagonists as agents in prevention of renal fibrosis
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批准号:8251867
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项目类别:
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资助金额:$38.96万
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财政年份:2012
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:7279669
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项目类别:
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资助金额:$0.1万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6892388
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项目类别:
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资助金额:$11.83万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6602379
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项目类别:
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资助金额:$11.31万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
Role of Glypicans in HGF Mediated Cell Morphogenesis
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批准号:6744097
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项目类别:
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资助金额:$11.56万
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财政年份:2003
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负责人:ANIL K KARIHALOO
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依托单位:
EPITHELIAL BRANCHING MORPHOGENESIS AND ENDOSTATIN
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批准号:6554742
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项目类别:
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资助金额:$5.44万
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财政年份:2002
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负责人:ANIL K KARIHALOO
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依托单位:
EPITHELIAL BRANCHING MORPHOGENESIS AND ENDOSTATIN
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批准号:6447271
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项目类别:
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资助金额:$4.73万
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财政年份:2001
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负责人:ANIL K KARIHALOO
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依托单位:
海外基金