Northern California Consortium for Sickle Cell Disease
北加州镰状细胞病联盟
基本信息
- 批准号:7224831
- 负责人:
- 金额:$ 13.49万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2006
- 资助国家:美国
- 起止时间:2006-04-18 至 2011-03-31
- 项目状态:已结题
- 来源:
- 关键词:Advisory CommitteesAdvocateAreaBiometryBloodBone Marrow TransplantationCaliforniaCell TransplantationCellsChildChildhoodCleaved cellClinicClinicalClinical ManagementClinical NursingClinical ResearchClinical TrialsCollaborationsCommitCommunitiesComprehensive Health CareCounselingDataDiseaseDisease-Free SurvivalElementsEngraftmentEnrollmentEnzymesErythropoiesisEvaluationExhibitsFamilyFatty AcidsGrowthGrowth and Development functionHematopoieticIndividualInjuryInvestigationLysophospholipidsMeasuresMedical centerMulticenter StudiesNatural HistoryNevadaOrganOrgan TransplantationOutcomePatient RecruitmentsPatientsPhasePhospholipase A2PhospholipidsPhysiciansProbabilityQuality of lifeRandomizedResearchResearch InfrastructureResearch PersonnelRiskSiblingsSickle Cell AnemiaStandards of Weights and MeasuresSupportive careTestingTherapeuticTherapeutic InterventionTransfusionabstractingacute chest syndromebasecollaborative trialcooperative studyexperiencefollow-uphydroxyureainternational centerpreventprospectiverhosickle erythropoiesis
项目摘要
DESCRIPTION (provided by applicant):
The Northern California Consortium for Sickle Cell Disease is a cohesive network of regional clinics and
comprehensive medical centers in Northern California and Nevada that are committed to providing comprehensive care for sickle cell disease. In addition, contributing centers in this Consortium have all the necessary elements that include physicians, nurses, clinical support staff, data coordinators, and clinical research infrastructure necessary to participate successfully in clinical trials for sickle cell disease. Efforts at patient recruitment will be enhanced by a partnership with the Community Advisory Committee, a community-based patient advocate organization in Northern California, by communicating with patients and their families about proposed clinical trials. Two clinical investigations are proposed in this application and involve areas in which the center in Oakland has a strong track record of clinical research. The first is a long-term follow-up evaluation after hematopoietic cell transplantation for sickle cell disease, which will be conducted in collaboration with the Center for International Blood and Marrow Transplantation Research (CIBMTR). This study will include a comparison of outcomes among children enrolled in the Cooperative Study of Sickle Cell Disease (CSSCD) and the multicenter pediatric hydroxyurea trial (HUG-KIDS), led by investigators in the Biostatistics team at Rho. The second investigation is a phase III randomized prospective trial of RBC transfusions to prevent acute chest syndrome in sickle cell disease. This investigation will target enrollment of sickle cell disease patients who exhibit high-risk features for acute chest syndrome, as evidenced by elevated levels of secretory phospholipase A2 (sPLA2), an enzyme which cleaves phospholipids generating fatty acids and lysophospholipids. Recently, we demonstrated that sPLA2 is dramatically elevated in many cases of ACS and rising sPLA2 levels predict ACS before it develops. The results of the proposed clinical trials are very likely to have a profound effect on the clinical management of patients with sickle cell disease, and both require a multicenter cooperative clinical trial infrastructure in order to complete these clinical investigations in a timely and rigorous manner. (End of Abstract)
描述(由申请人提供):
北加州镰刀细胞疾病联合会是一个由地区性诊所和
位于加利福尼亚州北部和内华达州的综合性医疗中心,致力于为镰状细胞疾病提供全面护理。此外,该联盟中的捐助中心拥有成功参与镰状细胞病临床试验所需的所有必要要素,包括医生、护士、临床支持人员、数据协调员和临床研究基础设施。通过与社区咨询委员会建立伙伴关系,与患者及其家人就拟议的临床试验进行沟通,将加强招募患者的努力。社区咨询委员会是加利福尼亚州北部的一个社区患者倡导组织。在这项申请中提出了两项临床研究,涉及奥克兰中心在临床研究方面有很强的记录。第一项是与国际血液和骨髓移植研究中心(CIBMTR)合作进行的镰状细胞病造血细胞移植后的长期随访评估。这项研究将包括对参加镰刀细胞病合作研究(CSSCD)和由Rho生物统计团队的研究人员领导的多中心儿科羟基尿素试验(HUG-KILDS)的儿童的结果进行比较。第二项研究是关于输注红细胞以预防镰状细胞病中的急性胸部综合征的III期随机前瞻性试验。这项研究将针对表现出急性胸部综合征高危特征的镰状细胞病患者进行登记,其证据是分泌型磷脂酶A2(SPLA2)水平升高,这是一种分解产生脂肪酸和溶血磷脂的磷脂的酶。最近,我们发现在许多急性冠脉综合征患者中sPLA2水平显著升高,并且sPLA2水平的升高在急性冠脉综合征发生之前就预示着它的发展。拟议的临床试验结果很可能对镰状细胞病患者的临床管理产生深远影响,两者都需要多中心合作的临床试验基础设施,以便及时和严格地完成这些临床研究。(摘要结束)
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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Mark C Walters其他文献
Exagamglogene Autotemcel for Severe Sickle Cell Disease.
Exagamglogene Autotemcel 治疗严重镰状细胞病。
- DOI:
10.1056/nejmoa2309676 - 发表时间:
2024 - 期刊:
- 影响因子:0
- 作者:
H. Frangoul;F. Locatelli;Akshay Sharma;Monica Bhatia;Markus Y. Mapara;Lyndsay Molinari;Donna A. Wall;Robert I Liem;Paul Telfer;Ami J Shah;Marina Cavazzana;S. Corbacioglu;D. Rondelli;Roland Meisel;Laurence Dedeken;S. Lobitz;M. de Montalembert;Martin H. Steinberg;Mark C Walters;Michael J. Eckrich;S. Imren;Laura Bower;C. Simard;Weiyu Zhou;Fengjuan Xuan;Phuong K Morrow;William E Hobbs;Stephan A Grupp - 通讯作者:
Stephan A Grupp
Defining curative endpoints for transfusion-dependent β-thalassemia in the era of gene therapy and gene editing.
定义基因治疗和基因编辑时代输血依赖性β-地中海贫血的治疗终点。
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
S. Corbacioglu;H. Frangoul;F. Locatelli;William E Hobbs;Mark C Walters - 通讯作者:
Mark C Walters
Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial
betibeglogene autotemcel基因疗法治疗输血依赖型严重基因型β-地中海贫血患者(HGB-212):一项非随机、多中心、单臂、开放标签、单剂量3期试验
- DOI:
10.1016/s0140-6736(24)01884-1 - 发表时间:
2024-11-30 - 期刊:
- 影响因子:88.500
- 作者:
Janet L Kwiatkowski;Mark C Walters;Suradej Hongeng;Evangelia Yannaki;Andreas E Kulozik;Joachim B Kunz;Martin G Sauer;Adrian J Thrasher;Isabelle Thuret;Ashutosh Lal;Ge Tao;Shamshad Ali;Himal L Thakar;Heidi Elliot;Ankit Lodaya;Ji Lee;Richard A Colvin;Franco Locatelli;Alexis A Thompson - 通讯作者:
Alexis A Thompson
Mark C Walters的其他文献
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{{ truncateString('Mark C Walters', 18)}}的其他基金
Curing Sickle Cell Disease with CRISPR-Cas9 genome editing
利用 CRISPR-Cas9 基因组编辑治疗镰状细胞病
- 批准号:
10336610 - 财政年份:2019
- 资助金额:
$ 13.49万 - 项目类别:
Curing Sickle Cell Disease with CRISPR-Cas9 genome editing
利用 CRISPR-Cas9 基因组编辑治疗镰状细胞病
- 批准号:
10264257 - 财政年份:2019
- 资助金额:
$ 13.49万 - 项目类别:
Northern California Consortium for Sickle Cell Disease
北加州镰状细胞病联盟
- 批准号:
7393717 - 财政年份:2006
- 资助金额:
$ 13.49万 - 项目类别:
Northern California Consortium for Sickle Cell Disease
北加州镰状细胞病联盟
- 批准号:
7059790 - 财政年份:2006
- 资助金额:
$ 13.49万 - 项目类别:
Induction of Stable Chimerism for Sickle Cell Anemia
镰状细胞性贫血稳定嵌合体的诱导
- 批准号:
6527795 - 财政年份:2001
- 资助金额:
$ 13.49万 - 项目类别:
Induction of Stable Chimerism for Sickle Cell Anemia
镰状细胞性贫血稳定嵌合体的诱导
- 批准号:
6804660 - 财政年份:2001
- 资助金额:
$ 13.49万 - 项目类别:
Induction of Stable Chimerism for Sickle Cell Anemia
镰状细胞性贫血稳定嵌合体的诱导
- 批准号:
6365241 - 财政年份:2001
- 资助金额:
$ 13.49万 - 项目类别:
Induction of Stable Chimerism for Sickle Cell Anemia
镰状细胞性贫血稳定嵌合体的诱导
- 批准号:
6576405 - 财政年份:2001
- 资助金额:
$ 13.49万 - 项目类别:
Induction of Stable Chimerism for Sickle Cell Anemia
镰状细胞性贫血稳定嵌合体的诱导
- 批准号:
6608590 - 财政年份:2001
- 资助金额:
$ 13.49万 - 项目类别:
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