Clinical Pharmacology (CP)
临床药理学(CP)
基本信息
- 批准号:8804008
- 负责人:
- 金额:$ 11.82万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1997
- 资助国家:美国
- 起止时间:1997-08-04 至 2019-11-30
- 项目状态:已结题
- 来源:
- 关键词:AliquotBiologicalBiological AssayBiological ProcessCancer Center Support GrantCellsClinicalClinical ChemopreventionClinical OncologyClinical PharmacologyClinical ResearchConcentration measurementConsultationsDNAData AnalysesDetectionDevelopmentDrug CombinationsDrug KineticsEpidemiologic StudiesEpidemiologyFacultyFluorescenceHigh Pressure Liquid ChromatographyImmunologyInvestigational DrugsInvestigational New Drug ApplicationLiquid substanceMalignant NeoplasmsMethodologyModelingMolecularNorris Cotton Cancer CenterPerformancePeripheral Blood Mononuclear CellPharmaceutical PreparationsPharmaceutical ServicesPharmacistsPharmacodynamicsPharmacologyPharmacology Shared ResourcePharmacy facilityPhasePlasmaProcessProtocols documentationResearchResearch DesignResearch MethodologyResearch PersonnelSalivaSamplingServicesSiteTestingTherapeuticTissuesTumor TissueUrineViolaabstractingbiobankcancer epidemiologycancer immunotherapycostdesignin vivoliquid chromatography mass spectrometrymembernoveloncologyoperationpharmacodynamic modelpre-clinicalprograms
项目摘要
Project Summary/Abstract: Clinical Pharmacology (CP)
The Clinical Pharmacology (CP) Shared Resource is now in its 19th year of operation and primarily functions
to support Norris Cotton Cancer Center (NCCC) investigators in the design, performance, data analysis, and
interpretation of pharmacology objectives in preclinical (in vivo and ex-vivo), clinical, chemoprevention, and
epidemiological studies, at lowest cost and highest value as possible. The major CPSR services are in 4
domains: (1) Central processing for biological fluids and tissues (e.g., cells, tumor tissue, plasma, saliva, urine,
DNA) obtained as part of approved clinical and epidemiological protocols; services that include, but are not
limited to, sample logging, processing (including processing peripheral blood mononuclear cells), aliquoting,
storage and sample distribution when necessary; (2a) Development of novel analyte assays (when such
assays are only available as research methods) using either high performance liquid chromatography (HPLC)
with ultra-violet (UV) and/or fluorescence detection, or increasingly liquid-chromatography mass spectrometry
(LC-MS/MS) methodology; (2b) Performance of analyte-concentration measurements in biological fluids and
tissues for preclinical and clinical oncology studies using these validated bioanalytical assays; (3a) Expert
consultation regarding study design and pharmacokinetic and pharmacodynamic hypothesis-development and
testing in preclinical and clinical cancer studies; (3b) Pharmacokinetic (PK) and pharmacodynamic (PD) data
analysis and PK-PD modeling from pre-clinical and clinical studies; and (4) Research pharmacy services for
cancer therapeutic clinical studies with both commercially available drugs and drugs under an investigational
new drug application (IND). CP is directed by Dr. Lionel D. Lewis, who has established expertise in the clinical
performance, the pharmacokinetics, and the pharmacodynamics of early phase clinical studies of
investigational oncology drug/drug combinations. Other staff include a junior faculty pharmacologist with
bioanalytical and molecular pharmacology expertise, a research assistant-lab manager with biorepository and
bioanalytical expertise, and a research pharmacist with expertise in oncologic and investigational drug
pharmacy. During the period 12/01/2012 to 11/30/2013, members of the Molecular Therapeutics (MT)
program were the most common and frequent users of CP services, representing 60% of use. However, CP
provided important services to other NCCC program members. Cancer Epidemiology (CE) members
represented 8.5% of users, Cancer Mechanisms (CM) members represented 8.5% of users, and Immunology
& Cancer Immunotherapy (ICI) program members represented 17% of users.
项目简介/摘要:临床药理学(CP)
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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LIONEL David LEWIS其他文献
LIONEL David LEWIS的其他文献
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{{ truncateString('LIONEL David LEWIS', 18)}}的其他基金
7HP349, an Integrin Activator to Treat Patients With anti-PD-1 Resistant Solid Tumors
7HP349,一种整合素激活剂,用于治疗抗 PD-1 耐药实体瘤患者
- 批准号:
10761171 - 财政年份:2023
- 资助金额:
$ 11.82万 - 项目类别:
Development of 7HP349, an oral integrin activator to enhance therapeutic responses to immune checkpoint inhibitors
开发 7HP349,一种口服整合素激活剂,可增强对免疫检查点抑制剂的治疗反应
- 批准号:
10261525 - 财政年份:2020
- 资助金额:
$ 11.82万 - 项目类别:
Toxicology, Pathology and Biodistribution Core (TPB Core)
毒理学、病理学和生物分布核心(TPB 核心)
- 批准号:
7982610 - 财政年份:2010
- 资助金额:
$ 11.82万 - 项目类别:
Protocol Review and Monitoring System (PRMS)
方案审查和监控系统 (PRMS)
- 批准号:
10554303 - 财政年份:1997
- 资助金额:
$ 11.82万 - 项目类别:
Protocol Review and Monitoring System (PRMS)
方案审查和监控系统 (PRMS)
- 批准号:
10311241 - 财政年份:1997
- 资助金额:
$ 11.82万 - 项目类别:
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