Developmental Therapeutics Research Program
发育治疗研究计划
基本信息
- 批准号:10456702
- 负责人:
- 金额:$ 8.49万
- 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:1997-04-25 至 2023-05-31
- 项目状态:已结题
- 来源:
- 关键词:Advanced Malignant NeoplasmAntibodiesApplied ResearchAwardBasic ScienceBiologicalBiological AssayBiological MarkersCancer CenterCancer PatientChildhoodClinicClinicalClinical ResearchClinical TrialsClinical Trials NetworkCollaborationsComprehensive Cancer CenterDevelopmentDevelopmental Therapeutics ProgramDirect CostsDiseaseDreamsDrug TargetingFundingGoalsHead CancerHematologic NeoplasmsImmunotherapyIndividualIndustry CollaborationInnovative TherapyInterventionInvestigational TherapiesLaboratoriesLeadMalignant NeoplasmsMalignant neoplasm of prostateMissionMolecularMolecular TargetMonitorNational Clinical Trials NetworkNeck CancerNeoplasm Circulating CellsNew AgentsOutcomePaperPathway interactionsPatient-Focused OutcomesPatientsPeer ReviewPeptidesPharmaceutical ChemistryPharmaceutical PreparationsPhasePhase I Clinical TrialsPreparationPublicationsPublishingRainReproduction sporesResearchResearch PersonnelResource SharingSchoolsScienceServicesSignal TransductionSolid NeoplasmSourceStrategic PlanningTherapeuticTherapeutic AgentsTherapeutic Human ExperimentationTimeTranslatingTranslational ResearchTranslationsUnited States National Institutes of HealthWorkanticancer researchbasebiomarker developmentbiomarker discoverycancer biomarkerscancer cellcancer clinical trialcancer therapyclinical translationcollegedata resourcedrug discoveryearly phase clinical trialeffective therapyfirst-in-humanimmune imagingimprovedinterdisciplinary approachmembernew therapeutic targetnovelnovel therapeuticspeerpre-clinicalpredictive testprogramsresearch and developmentresistance mechanismresponsesmall moleculetargeted agenttargeted cancer therapytherapeutic biomarkertherapeutic developmenttreatment strategytumor immunology
项目摘要
UWCCC Developmental Therapeutics (DT) Program Summary
Co-Leaders: Glenn Liu, Shigeki Miyamoto, and Jing Zhang
PROJECT SUMMARY/ABSTRACT
The mission of the UW Carbone Cancer Center (UWCCC) Developmental Therapeutics (DT) Program is to
improve cancer patient outcomes by discovering new targets, developing therapeutic agents and biomarkers,
and translating this research into early phase clinical trials. The DT Program provides the translational direction
not only for DT members, but for other programs within the UWCCC (e.g. GEM, VR, TM). Clinical trial data and
resources inform our understanding of response and resistance mechanisms and enable the identification of
new therapeutic targets and treatment strategies to improve clinical outcomes. The DT Program has 59 core
members, representing 18 departments and 5 different schools/colleges. Research impacts of DT members
are evidenced by research awards totaling over $22.5M in annual direct cost of peer-reviewed and non-peer
reviewed funding (including $3.45M NCI, $6.2M cancer-related other NIH agencies, $4.97M peer-reviewed
non-NIH sources, $7.9M non-peer reviewed funding) and a significant number of publications (1228
publications, 18% of which result from intra-programmatic collaboration and 24% from inter-programmatic
work).
A key component of the new UWCCC Strategic Operating Plan is to further strengthen and develop
Innovative Therapies and Cancer Biomarkers. Consistent with this strategic goal, the thematic aims of the
DT Program are to: 1) discover new molecular targets for cancer therapy; 2) develop new agents and
biomarkers; and 3) translate new therapies and biomarkers into clinical trials. To achieve this goal, it is critical
to have a very strong program that discovers, develops, and translates novel interventions and biomarkers. To
this end, members of the DT Program come from basic science, applied science, and clinical departments.
This program has expertise ranging from basic discovery (molecular pathways and targets), to development
(drugs/assays/biomarkers), to early clinical translation application (Phase 1 clinical trials). Translational and
clinical research DT program members apply intra- and inter-programmatic research discoveries in clinical
trials, performing the majority of first-in-human or early phase clinical trials, while individual disease-specific
research teams (Disease Oriented Teams) focus primarily on phase 2 and 3 studies. DT members lead or
participate in all clinical research groups facilitating both translational and reverse-translational opportunities.
UWCCC开发治疗学(DT)计划摘要
联合负责人:Glenn Liu、Shigeki Miyamoto和Jing Zhang
项目总结/摘要
UW Carbone癌症中心(UWCCC)开发治疗(DT)计划的使命是
通过发现新靶点、开发治疗剂和生物标志物,
并将这项研究转化为早期临床试验。DT计划提供了翻译方向
不仅适用于DT成员,而且适用于UWCCC内的其他计划(例如GEM,VR,TM)。临床试验数据和
资源为我们了解反应和抗性机制提供了信息,并使我们能够识别
新的治疗靶点和治疗策略,以改善临床结果。DT计划有59个核心
委员来自十八个学系及五间不同的学校/学院。DT成员的研究影响
证明了研究奖励总额超过2250万美元的年度直接成本的同行评审和非同行
审查的资金(包括345万美元的NCI,620万美元的癌症相关的其他NIH机构,497万美元的同行评审
非NIH来源,790万美元非同行评审资金)和大量出版物(1228
出版物,其中18%来自计划内合作,24%来自计划间合作
工作)。
新的UWCCC战略运营计划的一个关键组成部分是进一步加强和发展
创新疗法和癌症生物标志物。根据这一战略目标,
DT计划的目标是:1)发现癌症治疗的新分子靶点; 2)开发新的药物,
生物标志物;和3)将新疗法和生物标志物转化为临床试验。为了实现这一目标,
有一个非常强大的项目,发现,开发和翻译新的干预措施和生物标志物。到
为此,DT计划的成员来自基础科学,应用科学和临床部门。
该计划的专业知识范围从基本发现(分子途径和目标),
(药物/检测/生物标志物),到早期临床翻译应用(1期临床试验)。平移和
临床研究DT计划成员将计划内和计划间的研究发现应用于临床
试验,进行大多数首次在人体或早期临床试验,而个别疾病特异性
研究团队(疾病导向团队)主要专注于2期和3期研究。DT成员领导或
参与所有临床研究小组,促进翻译和反向翻译的机会。
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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{{ truncateString('Christian Capitini', 18)}}的其他基金
Exosome educated monocytes for acute radiation syndrome
外泌体训练的单核细胞治疗急性放射综合征
- 批准号:
10306061 - 财政年份:2021
- 资助金额:
$ 8.49万 - 项目类别:
Exosome educated monocytes for acute radiation syndrome
外泌体训练的单核细胞治疗急性放射综合征
- 批准号:
10458706 - 财政年份:2021
- 资助金额:
$ 8.49万 - 项目类别:
Combining hu14.18-IL2 and NK cell infusions to treat neuroblastoma
联合 hu14.18-IL2 和 NK 细胞输注治疗神经母细胞瘤
- 批准号:
10403986 - 财政年份:2018
- 资助金额:
$ 8.49万 - 项目类别:
Combining hu14.18-IL2 and NK cell infusions to treat neuroblastoma
联合 hu14.18-IL2 和 NK 细胞输注治疗神经母细胞瘤
- 批准号:
10194408 - 财政年份:2018
- 资助金额:
$ 8.49万 - 项目类别:
Inhibiting STAT1 as a novel graft-versus-host/graft-versus-leukemia therapy
抑制 STAT1 作为一种新型移植物抗宿主/移植物抗白血病疗法
- 批准号:
9264486 - 财政年份:2014
- 资助金额:
$ 8.49万 - 项目类别:
Inhibiting STAT1 as a novel graft-versus-host/graft-versus-leukemia therapy
抑制 STAT1 作为一种新型移植物抗宿主/移植物抗白血病疗法
- 批准号:
9057477 - 财政年份:2014
- 资助金额:
$ 8.49万 - 项目类别:
Inhibiting STAT1 as a novel graft-versus-host/graft-versus-leukemia therapy
抑制 STAT1 作为一种新型移植物抗宿主/移植物抗白血病疗法
- 批准号:
8699319 - 财政年份:2014
- 资助金额:
$ 8.49万 - 项目类别:
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