醫(yī)學(xué)專題-開發(fā)報(bào)批美國(guó)FDA的仿制藥與相關(guān)問(wèn)題探討

開發(fā)報(bào)批美國(guó)FDA的仿制(fǎngzhì)藥與相關(guān)問(wèn)題探討上海復(fù)星普適醫(yī)藥(yīyào)科技有限公司何平第一頁(yè)，共四十一頁(yè)。編輯ppt內(nèi)容提要(nèirónɡtíyào)開發(fā)仿制藥的重要性和機(jī)遇開發(fā)仿制藥的挑戰(zhàn)申報(bào)仿制藥的分類仿制藥研發(fā)團(tuán)隊(duì)仿制藥的研發(fā)過(guò)程QbD在制劑開發(fā)中怎么體現(xiàn)研發(fā)(高難)仿制藥的一些體會(huì)：案例(ànlì)研究第二頁(yè)，共四十一頁(yè)。編輯ppt開發(fā)(kāifā)仿制藥的重要性新藥與仿制藥-NDA

and

ANDA開發(fā)仿制藥與我國(guó)藥物研發(fā)的海外(hǎiwài)戰(zhàn)略藥物制劑目標(biāo)(mùbiāo)主流市場(chǎng)第三頁(yè)，共四十一頁(yè)。編輯ppt開發(fā)(kāifā)仿制藥的挑戰(zhàn)性開發(fā)(kāifā)仿制藥更具挑戰(zhàn)性藥物制劑專利仿制藥的競(jìng)爭(zhēng)仿制藥廠之間的競(jìng)爭(zhēng)由品牌藥轉(zhuǎn)成仿制藥第四頁(yè)，共四十一頁(yè)。編輯ppt仿制藥競(jìng)爭(zhēng)(jìngzhēng)的方式

HOWTOCOMPETECost-IRProductRawMaterialsProcessFinishedProductTechnology-ModifiedReleaseProducts第五頁(yè)，共四十一頁(yè)。編輯ppt申報(bào)(仿制(fǎngzhì))新藥的分類規(guī)范市場(chǎng)(FDA)1。P-I2。P-II3。P-III4。P-IV(1sttofile)中國(guó)(zhōnɡɡuó)市場(chǎng)（sFDA）1類2類3類4類5類6類第六頁(yè)，共四十一頁(yè)。編輯ppt仿制(fǎngzhì)藥研發(fā)團(tuán)隊(duì)

CONCEPT-1BUILDUPATEAMINFORMATIONFORMULATIONPRODUCTREGULATORYANALYTICALBIO-PHARMACEUTICALPROJECTLEGEL第七頁(yè)，共四十一頁(yè)。編輯pptDRUGDELIVERYSYSTEMSFORORALSOLIDFORMULATIONS-MRMATRIXSYSTEMSRESERVIORSYSTEMSOSMOTICALPUMPSYSTEMSCOMBO-SYSTEMS緩控釋給藥的技術(shù)平臺(tái)(píngtái)和給藥系統(tǒng)

CONCEPT-2BUILDUPASYSTEM第八頁(yè)，共四十一頁(yè)。編輯pptProductDevelopmentRoadmap仿制藥的研發(fā)(yánfā)過(guò)程第九頁(yè)，共四十一頁(yè)。編輯ppt?Quality–Acceptablylowriskoffailingtoachievethedesiredclinical

attributes?PharmaceuticalQuality=f{drugsubstance,excipients,manufacturing..}?QbD–‘Productandprocessperformancecharacteristicsscientificallydesignedtomeetspecificobjectives,notmerely

empiricallyderivedfromperformanceoftestbatches’WhatisQbD

(QualitybyDesign)?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？第十頁(yè)，共四十一頁(yè)。編輯pptWhatisQbD?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？PharmaceuticalQualitybyDesign(QbD)QbDmeansdesigninganddevelopingformulationsandmanufacturingprocessestoensurepredefinedproductqualityUnderstandingandcontrollingformulationandmanufacturingprocessvariablesaffectingthequalityofadrugproduct第十一頁(yè)，共四十一頁(yè)。編輯pptEssentialelementsofQbDDefinitionofthequalitytargetproductprofileHighlevelqualityaspectsoftheproduct:purity,drugrelease(dissolution/disintegrationtime),pharmacokineticprofile,etc.Criticalqualityattributes(CQAs)fordrugproduct?CharacteristicsofDPwhichhaveimpactondesiredprofile?ConsciousattempttostudyandcontrolCriticalProcessParameters(CPPs)?IdentificationofmaterialpropertiesandprocessparameterswhichhaveeffectonproductCQAsDesignSpace:ThemultidimensionalcombinationandinteractionofinputvariablesandprocessparametersthathavebeendemonstratedtoprovideassuranceofqualityIdentificationofacontrolstrategyforcriticalprocessparametersWhatisQbD?QbD在制劑開發(fā)中怎么(zěnme)體現(xiàn)？第十二頁(yè)，共四十一頁(yè)。編輯pptRawMaterialsEquipmentEnvironmentOperatorsVariable

Inputsx“Locked”Process=VariableQualityHowDidWeWorkinthePastWhatisQbD?QbD在制劑開發(fā)中怎么(zěnme)體現(xiàn)？第十三頁(yè)，共四十一頁(yè)。編輯pptRawMaterialsEquipmentEnvironmentOperatorsUnderstoodVariableInputsxUnderstoodandControlledProcess=PredefinedQualityFlexibleProcessDesignSpaceHowCanWeWorkintheFutureWhatisQbD?QbD在制劑開發(fā)(kāifā)中怎么體現(xiàn)？第十四頁(yè)，共四十一頁(yè)。編輯pptWhatisQbD?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompressionProduct第十五頁(yè)，共四十一頁(yè)。編輯pptDrugSubstanceExcipientsSourceAssayImpurities……LODPS

……WhatisQbD?QbD在制劑開發(fā)(kāifā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompression第十六頁(yè)，共四十一頁(yè)。編輯pptWaterBinderTempSprayRateSpeedTimeP.SWhatisQbD?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompression第十七頁(yè)，共四十一頁(yè)。編輯pptWhatisQbD?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompressionAirFlowTempRHShockCycleP.S.第十八頁(yè)，共四十一頁(yè)。編輯pptWhatisQbD?QbD在制劑開發(fā)(kāifā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompressionFillVolumeRotationSpeedEndPoint(Time)BlendUniformityDensitiesAngleofRepose第十九頁(yè)，共四十一頁(yè)。編輯pptWhatisQbD?QbD在制劑(zhìjì)開發(fā)中怎么體現(xiàn)？RawMaterialsWetGranulationFluidBedDryingBlendingCompressionFeedFrameToolingPunchPenetrationDepthCompression

ForcePressSpeedFeederSpeed……第二十頁(yè)，共四十一頁(yè)。編輯pptQualityAssessmentunderQbRQuestion-basedReview(QbR)isageneralframeworkforascienceandrisk-basedassessmentofproductqualityQbRcontainstheimportantscientificandregulatoryreviewquestionstoComprehensivelyassesscriticalformulationandmanufacturingprocessvariablesSetregulatoryspecificationsrelevanttoqualityDeterminethelevelofriskassociatedwiththemanufactureanddesignoftheproduct第二十一頁(yè)，共四十一頁(yè)。編輯pptExamplesofQbDquestionsunderQbR?ControlofDrugSubstance–Whatisthedrugsubstancespecification?Doesitincludeallthecriticaldrugsubstanceattributesthataffectthemanufacturingandqualityofthedrugproduct?(2pages)?DrugProduct–Whatattributesshouldthedrugproductpossess?(1.5pages)–Howweretheexcipientsandtheirgradesselected?–Howwasthefinalformulationoptimized??ManufacturingProcess–Howarethemanufacturingsteps(unitoperations)relatedtothedrugproductquality?–Howwerethecriticalprocessparametersidentified,monitored,and/orcontrolled??PharmaceuticalDevelopment?Manufacture?ContainerClosureSystem第二十二頁(yè)，共四十一頁(yè)。編輯pptAspectsTraditionalQbDPharmaceuticaldevelopmentEmpirical;univariateexperimentsSystematic;multivariateexperimentsManufacturingprocessFixed;validationon3initialfull-scalebatches;focusonreproducibilityAdjustablewithindesign

space;continuousverification;focusoncontrolstrategyProcesscontrolIn-processtestingforgo/nogo;offlineanalysisw/slowresponsePATutilizedforfeedback&feedforward,realtimeProductspecificationPrimarymeansofqualitycontrol;basedonbatchdataPartoftheoverallqualitycontrolstrategy;basedondesiredproductperformanceControlstrategyMainlybyintermediateandendproducttestingRisk-based;controlsshiftedupstream;real-timereleaseLifecyclemanagementReactivetoproblems&OOS;post-approvalContinuousimprovementenabledwithindesignspaceQbD小結(jié)(xiǎojié)-SUMMARY第二十三頁(yè)，共四十一頁(yè)。編輯ppt研發(fā)(yánfā)(高難)仿制藥的一些體會(huì)第二十四頁(yè)，共四十一頁(yè)。編輯ppt案例(ànlì)研究-1

CASESTUDY

1-IRTablets

VeryLowWaterSolubility(低水溶性)VeryLowPotency

(低劑量)MicronizedAPIused

(微粉化原料藥)WetGranulationProcess

(濕法制(fǎzhì)粒)第二十五頁(yè)，共四十一頁(yè)。編輯pptDissolution

Profile-體外溶出曲線(qūxiàn)第二十六頁(yè)，共四十一頁(yè)。編輯ppt生物(shēngwù)等效(BE)結(jié)果AUC0-tAUC0-infCmaxFastRatio108.01%108.12%86.26%90%GeometricC.I.103.49%to112.73%103.64%to112.79%75.28%to98.84%FedRatio111.21%112.48%85.24%90%GeometricC.I.104.40%to118.47%105.78%to119.60%73.47%to98.90%SummaryofinvivostudyresultsofTestFormulationvs.RLD第二十七頁(yè)，共四十一頁(yè)。編輯ppt原因(yuányīn)調(diào)查第二十八頁(yè)，共四十一頁(yè)。編輯ppt案例(ànlì)研究-2

CASESTUDY2-ERCAPSULESNoPatent

(無(wú)專利(zhuānlì))CoatedPellets

(包衣微丸)1stBioStudyFailedFast:CloseFed(ComparedwithFast):Brand:BAReducedTested:BAIncreased第二十九頁(yè)，共四十一頁(yè)。編輯pptTEAMWORKMoreInformationCollectedAnalyticalSupportIdentifytheProcessUsedProvidetheInfoforFunctionalCoatingOnemorePilotandOneFullBioPassed第三十頁(yè)，共四十一頁(yè)。編輯ppt案例(ànlì)研究-3

CASESTUDY3-ERCAPSULESBrandProductMicro-TabletsinCapsules95%ofAPIexistedinFinishedProductSystemandProcessPatented第三十一頁(yè)，共四十一頁(yè)。編輯pptUNIQUESYSTEM-CREATIVEDESIGNCompressedGranulesinCapsulesRequirementSameDissolutionBehaviorUniformYieldAcceptable第三十二頁(yè)，共四十一頁(yè)。編輯pptSYSTEMCOMPARISON第三十三頁(yè)，共四十一頁(yè)。編輯pptPILOTBIO-STUDYPRODUCTPDATA(LogTransformedData,Fast,n-12)RatioofGeometricMeansx10090%CIofLogTransformedDataCV(%)TestAvsReferenceAUC10690.4;12322.0Cmax10480.1;13436.4TestBvsReferenceAUC133114;15522.0Cmax129100;16736.4第三十四頁(yè)，共四十一頁(yè)。編輯pptPILOTBIO-STUDYPRODUCTPDATA(LogTransformedData,FED,n-11)RatioofGeometricMeansx10090%CIofLogTransformedDataCV(%)TestAvsReferenceAUC96.175.4;12332.7Cmax10983.5;14135.3TestBvsReferenceAUC92.472.5;11832.7Cmax10983.7;14135.3第三十五頁(yè)，共四十一頁(yè)。編輯pptPIVOTALBIO-STUDYPRODUCTPDATA(LogTransformedData)RatioofGeometricMeansx10090%CIofLogTransformedDataCV(%)FAST