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Brittle Bone Disorders Consortium of the Rare Disease Clinical Research Network

Brittle Bone Disorders Consortium of the Rare Disease Clinical Research Network
罕见疾病临床研究网络脆性骨疾病联盟
批准号:
8906760
负责人:
Brendan Lee
金额:
$126.16万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-06 至 2019-07-31
关键词:
AdultAdvocacyAffectAntibodiesBaltimoreBiochemistryBiological MarkersBiometryBone DiseasesBoxingCanadaChicagoChildChildhoodClinicalClinical ResearchClinical TreatmentCollagenCollagen GeneCollagen Type IComplexDataDeformityDentalDevelopmentDiagnosisDiagnostics ResearchDiseaseDistrict of ColumbiaDoseE-learningEducational workshopEpidemiologyFacultyFamilyFellowshipFloridaFoundationsFractureGenderGenesGenetic Predisposition to DiseaseGenotypeHealth PersonnelHealth SciencesHereditary DiseaseHeterogeneityHospitalsHumanHuman Subject ResearchHydroxylationIndustryInformation SystemsInstitutesKnowledgeLeadLifeLinkLos AngelesMass Spectrum AnalysisMeasurementMeasuresMedicalMedical GeneticsMedical StudentsMedical centerMedicineMolecular GeneticsMutationNatural HistoryNew YorkNew York CityObservational StudyOperative Surgical ProceduresOregonOsteogenesis ImperfectaOutcomePatient Outcomes AssessmentsPatient advocacyPatientsPatternPhasePhenotypePhysiciansPilot ProjectsPost-Translational Protein ProcessingPregnancyPrimary Health CarePrincipal InvestigatorRaceRare DiseasesRecruitment ActivityResearchResearch PersonnelResearch TrainingResourcesRotationSeveritiesSeverity of illnessSignal PathwaySignal TransductionSignaling ProteinSiteSpecial HospitalsSpinal FracturesStructureSystemTestingTherapeuticTrainingTranslatingUniversitiesWagesWashingtonbasebiomechanical engineeringboneburden of illnesschronic painclinical research sitecohortcollegecontrol trialcraniofacialcrosslinkdesigndisease natural historymembermouse modelmultidisciplinarynovelphase I trialpreclinical studypublic health relevanceresearch studyresponsescoliosisskeletalsuccesstherapeutic targettooltraffickingurinary

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DESCRIPTION (provided by applicant): This is an application to establish a Brittle Bones Disorders Rare Disease Clinical Research Consortium (BBD RDCRC) focused on studying the over 13 genetic conditions that not contribute to the Osteogenesis Imperfecta (OI) phenotype. The BBD RDCRC is composed of 8 primary clinical sites (Houston, Los Angeles, Portland, Chicago, Montreal, New York City, Baltimore, Washington DC), 2 core sites (Seattle and Tampa), one training & advocacy site (Osteogenesis Imperfecta Foundation), and an Administrative unit (Houston). We propose two clinical projects. Project 1 is a Longitudial study of OI focused on correlating genotype to phenotype, natural history of vertebral fractures in OI type I, scoliosis in severe OI, pregnancy i OI, and craniofacial/dental features in severe Ol. Project 2 is a Phase I trial of an anti-TGFb therapy Fresolimumab in severe OI in the context of a dose ranging study followed by an extension repeat dosing study. There will be two Pilot Projects. The first focuses on the development of mass spectrometric analysis of urinary collagen cross-link patterns as a tool for distinguishing different mechanistic causes of Ol and for correlating with disease severity. The second focuses on validating aspects of the PROMIS tool for adults with OI. An important partner will be the Osteogenesis Imperfecta Foundation (OIF) and the Training and Advocacy activities will be coordianted by the OIF. They include establishment of a new fellowship for clinical research training, a clinical bone research training workshop, and development of a "tool box" of web-based training for primary healthcare providers to extend the knowledge gained by these studies to patients. Finally, the administration of the BBD RDCRC will be based in Houston at the Baylor College of Medicine. The BBD RDCRC will be leveraged by resources from the OIF who will directly support two of the clinical sites and a pilot project on PROMIS, the Shriners Hospital system, and institutional commitments from Baylor College of Medicine. The BBD RDCRC is built on established cohorts of the OIF Linked Longitudinal Clinical Research Centers and established expertise in pediatric and adult interventional studies that demonstrates a track record of success in patient advocacy, recruitment, and retention for clinical research studies.
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