findmyKOL
Clinical trialNCT04334707RecruitingObservational

Kidney Precision Medicine Project

SponsorIcahn School of Medicine at Mount SinaiEnrollment1,000Acute Kidney FailureAcute Kidney InsufficiencyAcute Renal FailureAcute Renal InjuryAcute Renal InsufficiencyChronic Kidney Diseases+9 more conditions
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Acute kidney injury (AKI) and chronic kidney disease (CKD) impose a significant global health burden. Yet, no effective therapies currently exist for AKI, and only a few are available for CKD. Despite significant effort from industry and academia, development of pharmacologic therapies for AKI and CKD has been hampered by: Non-predictive animal models The inability to identify and prioritize human targets The limited availability of human kidney biopsy tissue A poor understanding of AKI and CKD heterogeneity Historically, AKI and CKD have been described as single, uniform diseases. However, growing consensus suggests that different disease pathways lead to different subgroups of AKI and CKD (AKIs and CKDs). Access to human kidney biopsy tissue is a critical first step to define disease heterogeneity and determine the precise molecular pathways that will facilitate identification of specific drug targets and ultimately enable individualized care for people with AKI and CKD. A number of research centers across the United States are collaborating to bring state-of-the-art technologies together to: * Ethically obtain and evaluate kidney biopsies from participants with AKI or CKD * Define disease subgroups * Create a kidney tissue atlas * Identify critical cells, pathways, and targets for novel therapies The KPMP is made up of three distinct, but highly interactive, activity groups: * Recruitment Sites: The recruitment sites (RS) are responsible for recruiting participants with AKI or CKD into the longitudinal study and performing the kidney biopsy. * Tissue Interrogation Sites: The tissue interrogation sites (TIS) are responsible for developing and using innovative technologies to analyze the biopsy tissue. * Central Hub: The central hub is responsible for aggregating, analyzing, and visualizing the generated data and providing scientific, infrastructure, and administrative support for the KPMP consortium.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of Arizona

    Tucson, Arizona, United States

    Frank "Chip" Brosius, MD
    Recruiting
  • Yale University

    New Haven, Connecticut, United States

    Dennis Moledina, MBBS, PhDFrances (Perry) Wilson, MD
    Recruiting
  • University of Illinois Chicago

    Chicago, Illinois, United States

    Ana Ricardo, MDJames Lash, MD
    Recruiting
  • Johns Hopkins University

    Baltimore, Maryland, United States

    Chirag Parikh, MD, PhDSteve Menez, MD
    Recruiting
  • Boston Medical Center

    Boston, Massachusetts, United States

    Sushrut Waikar, MD
    Recruiting
  • Joslin Diabetes Center

    Boston, Massachusetts, United States

    Stewart Lecker, MDSylvia Rosas, MD
    Recruiting
  • University of Minnesota

    Minneapolis, Minnesota, United States

    Luiza Caramori, MDPatrick Nachman, MD
    Recruiting
  • Mayo Clinic, Rochester

    Rochester, Minnesota, United States

    Aleksandra Kukla, MDYogish Kudva, MD
    Recruiting
  • Mount Sinai

    New York, New York, United States

    Kristin Meliambro, MDSteven Coca, DO
    Recruiting
  • University of North Carolina

    Chapel Hill, North Carolina, United States

    Amy Mottl, MD
    Recruiting
  • Cleveland Clinic

    Cleveland, Ohio, United States

    Emilio Poggio, MDJohn O'Toole, MDJohn Sedor, MD
    Recruiting
  • University of Texas at Southwestern

    Dallas, Texas, United States

    Miguel Vazquez, MDRobert Toto, MD
    Recruiting
  • University of Washington

    Seattle, Washington, United States

    Ian de Boer, MDPetter Bjornstad, MD
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 Sept 2019
Primary completion
30 Jun 2027
Completion
30 Jun 2027
Last update posted
14 Apr 2026
Registered enrollment
1,000
Registry id
NCT04334707

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.