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Clinical trialNCT04724837CompletedPhase 2Interventional

Zibotentan and Dapagliflozin for the Treatment of CKD (ZENITH-CKD Trial)

SponsorAstraZenecaEnrollment542Chronic Kidney Disease
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of the study is to assess efficacy, safety and tolerability of treatment with zibotentan and dapagliflozin in combination and dapagliflozin 10 mg as monotherapy in participants with chronic kidney disease (CKD) with estimated glomerular filtration rate (eGFR) ≥ 20 mL/min/1.73 m\^2, and urinary albumin to creatinine ratio (UACR) ≥ 150 mg/g and ≤ 5000 mg/g.

Investigators

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

  • David C Wheeler, MB ChB, MD, FRCP

    Centre for Nephrology Royal Free Campus University College London Rowland Hill Street London NW3 2PF United Kingdom

    Principal Investigator
  • Jamie P. Dwyer, M.D.

    Nephrology Clinical Trials Center Nephrology and Hypertension Vanderbilt University Medical Center Nashville TN United States of America

    Principal InvestigatorKOL profile →

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

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

Argentina
  • Research Site

    Buenos Aires, Argentina

  • Research Site

    CABA, Argentina

  • Research Site

    CABA, Argentina

  • Research Site

    Corrientes, Argentina

  • Research Site

    Córdoba, Argentina

  • Research Site

    Junín, Argentina

  • Research Site

    Mar del Plata, Argentina

  • Research Site

    Mar del Plata, Argentina

  • Research Site

    San Luis, Argentina

  • Research Site

    San Miguel de Tucumán, Argentina

  • Research Site

    Santa Fe, Argentina

Australia
  • Research Site

    Adelaide, Australia

  • Research Site

    Birtinya, Australia

  • Research Site

    Elizabeth Vale, Australia

  • Research Site

    Gosford, Australia

  • Research Site

    Westmead, Australia

Brazil
  • Research Site

    Botucatu, Brazil

  • Research Site

    Campinas, Brazil

  • Research Site

    Curitiba, Brazil

  • Research Site

    Porto Alegre, Brazil

  • Research Site

    Santo André, Brazil

  • Research Site

    São José do Rio Preto, Brazil

  • Research Site

    São Paulo, Brazil

  • Research Site

    São Paulo, Brazil

  • Research Site

    São Paulo, Brazil

Bulgaria
  • Research Site

    Gabrovo, Bulgaria

  • Research Site

    Kozloduy, Bulgaria

  • Research Site

    Montana, Bulgaria

  • Research Site

    Plovdiv, Bulgaria

  • Research Site

    Sliven, Bulgaria

  • Research Site

    Sofia, Bulgaria

  • Research Site

    Sofia, Bulgaria

  • Research Site

    Stara Zagora, Bulgaria

Canada
  • Research Site

    St. John's, Newfoundland and Labrador, Canada

  • Research Site

    London, Ontario, Canada

  • Research Site

    Toronto, Ontario, Canada

  • Research Site

    Waterloo, Ontario, Canada

Croatia
  • Research Site

    Pula, Croatia

  • Research Site

    Vinkovci, Croatia

Denmark
  • Research Site

    Gentofte Municipality, Denmark

124 more sites on the registry record.ClinicalTrials.gov ↗

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

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Dapagliflozin →PlaceboZibotentan
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

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

Start
28 Apr 2021
Primary completion
1 Jun 2023
Completion
1 Jun 2023
Last update posted
30 Jul 2024
Registered enrollment
542
Registry id
NCT04724837

Cross-registrations

EU-CTR / CTIS (EudraCT)2020-004101-32

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.