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Phase I Trials of Anti-Cancer Agents

Phase I Trials of Anti-Cancer Agents
抗癌药物的一期试验
批准号:
8628946
负责人:
MICHAEL R GREVER
金额:
$75.49万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-04-15 至 2015-02-28
关键词:
Antineoplastic AgentsApoptosisBasic ScienceBiological AssayBiological SciencesBiomedical ResearchCancer CenterCancer PatientCancer Therapy Evaluation ProgramCell Cycle RegulationCell SurvivalChildhoodClinicClinicalClinical ResearchClinical SciencesClinical TrialsClinical assessmentsComprehensive Cancer CenterConduct Clinical TrialsCorrelative StudyDataDentistryDevelopmentDiscipline of NursingDiseaseDoseDrug Administration ScheduleDrug KineticsEngineeringEvaluationExposure toFacultyFunctional ImagingFunctional disorderGoalsHepaticHistonesHumanIndividualIntentionInterdisciplinary StudyInvestigationInvestigational DrugsInvestigational TherapiesJointsKidneyKnowledgeLaboratoriesLaboratory StudyMalignant - descriptorMalignant NeoplasmsMeasurementMedicineMethylationMissionMolecularMolecular GeneticsMolecular TargetMonoclonal AntibodiesNational Cancer InstituteNew AgentsOhioOutcomePatientsPharmaceutical PreparationsPharmacodynamicsPharmacogenomicsPharmacy facilityPhasePhase I Clinical TrialsPlayPopulationPost-Translational Protein ProcessingProcessProtocols documentationPublic HealthRecommendationRegimenRegulationResearch DesignResearch PersonnelRoleSafetyScheduleSchemeScientistSignal PathwaySignal Transduction PathwayTherapeuticTherapeutic AgentsTherapeutic Human ExperimentationTimeToxic effectUniversitiesVariantVeterinary Medicineangiogenesisbasecancer therapyclinical effectcollegecritical perioddesignexperiencemannamed groupneoplastic cellnovelnovel therapeuticspatient safetyphase 1 studyphysical sciencepre-clinicalprogramsresponsetherapeutic targettumor

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DESCRIPTION (provided by applicant): Phase I studies play a critical role in the development of new cancer therapies. These trials are the initial interface between basic and clinical research for "first in human" studies. Successful therapeutic research embodies an iterative process between the clinic and the laboratory during this critical period of initial development. Whereas in the past, phase I trials focused strictly upon defining the toxicity and pharmacokinetics of new agents, the current emphasis requires that more information is efficiently procured without compromising the analysis of safe and effective administration. This mandate requires real-time procurement of pharmacokinetics, pharmacodynamics, and pharmacogenomics as well as meticulous clinical assessment. In this application, both clinical and basic science investigators of The Ohio State University Comprehensive Cancer Center (OSUCCC) join in a collaborative approach to conduct phase I trials of new cancer therapeutic agents and regimens. Investigators will cooperate closely with the National Cancer Institute in developing correlative studies to evaluate clinical outcomes in the context of basic science observations. The present application builds upon approximately 30 years of experience and the scientific strength of the OSUCCC in conducting clinical trials with pertinent biologic measurements. Trials will target agents and strategies with which our faculty has prior preclinical experience and/or cellular and molecular networks under study in their laboratories. The Experimental Therapeutics Program at OSUCCC has expertise in signal transduction pathways, angiogenesis, cell cycle control, selective induction of tumor cell apoptosis, monoclonal antibodies, molecular genetics, histone protein modification, DMA methylation and other basic targeted therapeutic strategies. The Ohio State University represents one of the most comprehensive biomedical research campuses in the world dedicated to interdisciplinary research. Respective scientists associated with experimental therapy of cancer form a critical mass within the Colleges of Medicine and Public Health, Pharmacy, Biological Sciences, Mathematical and Physical Sciences, Veterinary Medicine, Engineering, Dentistry, and Nursing. This is a Phase I clinical trials program designed to achieve the ultimate goals of expedient (yet thorough) dose-finding trials in man with the intention of providing safe and effective new therapy to benefit patients with malignant diseases.
期刊论文(52)
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科研奖励(0)
会议论文
DOI: 10.1007/s10637-010-9563-7
发表时间: 2012-04
期刊: INVESTIGATIONAL NEW DRUGS
影响因子: 3.4
作者: [Ramaswamy, Bhuvaneswari, Phelps, Mitch A., Baiocchi, Robert, Bekaii-Saab, Tanios, Ni, Wenjun, Lai, Ju-Ping, Wolfson, Anna, Lustberg, Mark E., Wei, Lai, Wilkins, Deidre, Campbell, Angela, Arbogast, Daria, Doyle, Austin, Byrd, John C., Grever, Michael R., Shah, Manisha H.]
通讯作者: Shah, Manisha H.
DOI: 10.1007/s10637-012-9863-1
发表时间: 2013-06
期刊: INVESTIGATIONAL NEW DRUGS
影响因子: 3.4
作者: [Mortazavi, Amir, Ling, Yonghua, Martin, Ludmila Katherine, Wei, Lai, Phelps, Mitch A., Liu, Zhongfa, Harper, Erica J., Ivy, S. Percy, Wu, Xin, Zhou, Bing-Sen, Liu, Xiyong, Deam, Deidre, Monk, J. Paul, Hicks, William J., Yen, Yun, Otterson, Gregory A., Grever, Michael R., Bekaii-Saab, Tanios]
通讯作者: Bekaii-Saab, Tanios
DOI: 10.1371/journal.pone.0074710
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Nicholas C, Yang J, Peters SB, Bill MA, Baiocchi RA, Yan F, Sïf S, Tae S, Gaudio E, Wu X, Grever MR, Young GS, Lesinski GB]
通讯作者: Lesinski GB
Development and validation of a rapid and sensitive high-performance liquid chromatography-mass spectroscopy assay for determination of 17-(allylamino)-17-demethoxygeldanamycin and 17-(amino)-17-demethoxygeldanamycin in human plasma.
开发和验证快速、灵敏的高效液相色谱-质谱法测定人血浆中的 17-(烯丙氨基)-17-去甲氧基格尔德霉素和 17-(氨基)-17-去甲氧基格尔德霉素。
DOI: 10.1016/j.jchromb.2008.06.029
发表时间: 2008
期刊: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
影响因子: --
作者: [Johnston,JeffreyS, Phelps,MitchA, Blum,KristieA, Blum,William, Grever,MichaelR, Farley,KatherineL, Dalton,JamesT]
通讯作者: Dalton,JamesT
18
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