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Development of A Novel Anti-Hyperglycemic Agent

Development of A Novel Anti-Hyperglycemic Agent
新型抗高血糖药的研制
批准号:
7687310
负责人:
Zhaoping Li
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2012-03-31
关键词:
Adverse effectsAdverse eventAgreementAlzheimer&aposs DiseaseAmino AcidsAnimal ModelAnimalsAsiansBloodBlood GlucoseBone DensityBrainCardiovascular systemCause of DeathCell membraneCellsCenters for Disease Control and Prevention (U.S.)ChemistryChronic DiseaseClinicalClinical TrialsComplexCopperCountryCytosolDefectDevelopmentDiabetes MellitusDiabetes preventionDipeptidesDiseaseDoseDouble-Blind MethodDropsEnvironmental Risk FactorEnzyme GeneEnzymesEuropeanEventExpenditureFDA approvedFastingFutureGelGenesGeneticGenetic PolymorphismGlucagonGlucoseGlucose IntoleranceGlucose TransporterGlucose tolerance testGlycosylated hemoglobin AHealthHealthcareHematologyHepaticHigh PrevalenceHourHumanHyperglycemiaHypoglycemiaHypoglycemic AgentsImpairmentInjection of therapeutic agentInpatientsInsulinInsulin ReceptorInsulin ResistanceInsulinaseIntakeIntestinesKidneyLeadLegal patentLeptinLiteratureLiverLiver FailureMarketingMediatingMedicalMedical centerMetforminMolecularMuscleMutationNational Health and Nutrition Examination SurveyNauseaNon-Insulin-Dependent Diabetes MellitusObesityOralOral AdministrationOutcomeOutcome StudyOutpatientsPatientsPeptide HydrolasesPeptidesPeripheralPharmaceutical PreparationsPharmacy facilityPhasePhase I Clinical TrialsPioglitazonePlacebo ControlPlacebosPlasmaPlayPopulationPreventionProcessProteinsRandomizedRattusReceptor SignalingRecruitment ActivityRegimenReportingResearchResearch DesignRiskRoleSLC2A1 geneSafetyServicesSevere Adverse EventSignal TransductionStomachSulfonylurea CompoundsSymptomsTherapeutic AgentsThyroid Function TestsTissuesUnited StatesUrineVeteransVisitVomitingZincZinc deficiencyabsorptionadiponectinanalogbasebrain tissuecapsulecommercializationcostdiabeticdiabetic patientdiet and exerciseeffective therapyexperiencefasting plasma glucosefour-arm studyfunctional disabilityglucogenesisglucose metabolismglucose outputglucose uptakeglycemic controlhistidylprolineimprovedinhibitor/antagonistinsulin sensitivityinsulin signalingnoveloral glucose toleranceprimary outcomepublic health relevancereceptor recyclingrosiglitazonesecondary outcomevolunteerweek trial

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DESCRIPTION (provided by applicant): We have demonstrated that a cyclic dipeptide Cyclo (his-pro) plus zinc (Cyclo-Z) treatment improved clinical conditions of diabetes in various animal models and a phase 1 clinical trial. The main objective of this study is to demonstrate that this product is safe and effective for the treatment of human diabetes. Research Plan This is a randomized, double blinded, placebo-controlled, and parallel study. In this study, we will recruit 120 hypoglycemic drug naove type 2 diabetic patients and randomize them into 4 groups of 30 subjects each to compare the effects of a Cyclo-Z capsule containing CHP 0 (placebo), 3 mg (minimally effective), 9 mg (optimally effective), or 15 mg (no-additional effect) plus 20 mg zinc on diabetic symptoms in a 12-week trial period. The primary outcome of this study is improvement of hemoglubin A1c; secondary outcomes are fasting blood glucose, 2 hours postprandial glucose and glucose tolerance test. Safety will be assessed by the presence of severe adverse events (SAEs), adverse events (AEs), any changes of vital signs, physical exams, blood hematology, chemistry, liver, renal, thyroid function tests, urine analysis and zinc, copper levels. PUBLIC HEALTH RELEVANCE: Relevance to the Veterans Health Diabetes is a difficult and challenging chronic disease, and the seventh leading cause of death in the US (61). The DVA provides healthcare service to about 5.0 million patients throughout the country in 163 medical centers, and diabetes has high prevalence in VA patients. In the year 2000, 19.6% of VA patients had diabetes and this percentage increases annually by 2 % (61). Hence, the diabetic population among VA patients may approach 30% in the year 2008. About 30 % of pharmacy prescriptions of the VA Medical Centers are received by diabetic patients (62) and overall 23 % of pharmacy expenditures were related to patients' glycemic control in the year 2000. The expenditure for the outpatient visits was $214.8 million and inpatient expenditure was $1.45 billion in 1998 (63). Cyclo-Z may pose a benefit to more than 30% of veteran population. This new drug may ameliorate diabetes and reduce insulin-resistance which would greatly reduce the cost of inpatient and outpatient medical service as well as pharmacy expenditure. Three different patents with Cyclo-Z for the treatment of diabetes, obesity and Alzheimer's disease are now owned by the DVA and the phase 1 clinical trial has been completeds with favorable result. The outcome of the proposed phase 2a clinical trial will lead to an agreement with a major drug company by the DVA for Cyclo-Z marketing. We believe that Cyclo-Z will be effective and safe in the prevention and treatment of diabetes and that this novel drug will be beneficial to the health of many diabetic veteran patients.
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BCAA Catabolic Defect in HF: Novel Mechanism and Therapeutic Target
Development of A Novel Anti-Hyperglycemic Agent
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