grant

Predoctoral Preparatory Program (P3) in Translational Research

Organization CHILDREN'S HOSP OF PHILADELPHIALocation PHILADELPHIA, UNITED STATESPosted 1 May 2024Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY20250-11 years oldAddison disease-cerebral sclerosis syndromeAddison disease-spastic paraplegia syndromeAddison-Schilder syndromeAddressAdrenoleukodystrophyAffectAgeAreaArylsulfatase A Deficiency DiseaseBronze Schilder diseaseCareer ChoiceCareer ExplorationCareer PathCerebroside Sulphatase Deficiency DiseaseCerebrumChildChild YouthChildhoodChildren (0-21)Children's HospitalClinical ResearchClinical StudyClinical Trials NetworkCollaborationsCollectionCommunicationCommunitiesComplex thinkingCritical ThinkingCurriculumDNA TherapyDevelopmentDevelopment PlansDevelopment and ResearchDiseaseDisorderEducationEducational CurriculumEducational aspectsEducational process of instructingEducational workshopEnrollmentEnvironmentEvaluative ThinkingExposure toFanconi-Prader syndromeFoundationsFundingFutureGene Transfer ClinicalGenetic InterventionGoalsHourIndividualInfrastructureInstitutionInternetInvestigatorsLeadMedicineMentorsMentorshipMetachromatic LeukodystrophyMyelinNational Institutes of HealthNeurologicNeurologicalOrphan DiseasePb elementPediatric HospitalsPennsylvaniaPersonal awarenessPersonsPhiladelphiaPhysiciansPopulationProcessR & DR&DRare DiseasesRare DisorderResearchResearch PersonnelResearch ResourcesResearchersResourcesSchilder-Addison ComplexScienceScientistSelf PerceptionSelf imageSelf viewSiemerling-Creutzfeldt diseaseSiemerling-Creutzfeldt syndromeSiteSulfatide LipidosisSulfatidosisTargeted ResearchTeachingTherapeuticTranslational ResearchTranslational ScienceUnderrepresented GroupsUnderrepresented PopulationsUnited States National Institutes of HealthUniversitiesWWWWorkWorkshopX-Linked Adrenoleukodystrophyadrenocortical atrophy-cerebral sclerosis syndromeadrenoleukomyeloneuropathyagesarylsulfatase A deficiencycareercareer aspirationcareer developmentcareer interestcareer pathwaycareer trackcerebralcommunity buildingconferenceconventiondesigndesigningdevelop therapydevelopmentalenrollexpectationexperiencegene repair therapygene therapygene-based therapygenetic therapygenomic therapyhands on researchheavy metal Pbheavy metal leadinnovateinnovationinnovativeinterestintervention developmentkidslesson plansleukodystrophymedical collegemedical schoolsmeetingmeetingsmelanodermic leukodystrophymetachromatic leukoencephalopathymetachromatic leukoencephalynext generationnovelorphan disorderpediatricpre-docpre-doctoralprogramsrare genetic diseaserare genetic disorderrecruitresearch and developmentresponsible research conductschool of medicineself awarenessself knowledgeskill acquisitionskill developmentskillssulfatide lipoidosissummitsymposiasymposiumtargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmenttherapeutic agent developmenttherapeutic developmenttherapy developmenttooltranslation researchtranslational investigationtranslational investigatortranslational medicinetranslational researchertranslational scientisttranslational therapeuticstranslational therapytreatment developmentunder representation of groupsunder represented groupsunder represented peopleunder represented populationsunderrepresentation of groupsunderrepresented peoplewebworld wide webyoungster
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Full Description

Project Summary/Abstract
Leukodystrophies are a collection of rare genetic disorders that affect cerebral myelin development.

Exciting recent therapeutic advances, including gene therapy development for adrenoleukodystrophy

and metachromatic leukodystrophy, underscore the critical unmet need for therapeutic development

more broadly across the leukodystrophies. The future of innovation, however, is limited by the pipeline

of future translational researchers interested in rare diseases.

The Rare Diseases Clinical Research Network (RDCRN) Global Leukodystrophy Initiative Clinical Trials

Network (GLIA-CTN; U54TR002823) is an NIH-funded research consortium for leukodystrophy

collaboration and innovation across a network of 8 large US-based academic institutions. This

infrastructure provides a unique opportunity to recruit and support the next generation of rare disease

research leaders. We hypothesize that a formal education program in rare disease research targeting

junior research coordinators who are early in their career will facilitate long-term commitment and

passion for rare disease research. This is a population that is enriched with young scholars interested

in science who are often undecided about career paths or have had insufficient exposure to translational

research. The proposed program represents a novel collaboration between the Leukodystrophy Center

of Excellence (LCE) at the Children’s Hospital of Philadelphia (CHOP), a GLIA-CTN site, and the

Institute for Translational Medicine and Therapeutics Education (ITMAT Ed) programs at the Perelman

School of Medicine, University of Pennsylvania. In 2021-2022, the LCE and ITMAT Ed piloted the

Predoctoral Preparatory Program (P3) with 8 junior research coordinators, known as P3 scholars, based

exclusively within the Children’s Hospital of Philadelphia (CHOP). In 2022-2023, the program expanded

to include 14 coordinators working at sites across the GLIA-CTN. Each year we aim to enroll 12-15

scholars who are junior research coordinators working within the GLIA-CTN. We recognize the

importance of diversity among future translational research leaders and will continue to recruit from

populations underrepresented in medicine (UIM).

In this application, we propose an education program, the Predoctoral Preparatory Program (P3),

which will (1) provide a curriculum related to responsible conduct of research and (2) prepare the next

generation of physician scientists in translational research through professional development workshops

and mentorship. This proposal is to further the development and implementation of a one-year program

focused on research and professional skills development, community building, and mentorship which is

fully integrated into a hands-on research experience through the GLIA-CTN research network.

Grant Number: 5R25TR005269-02
NIH Institute/Center: NIH

Principal Investigator: Laura Adang

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