πŸ›οΈ Verified NIH Record β€’ Updated 2026-05-15

A Phase IIb Study to Evaluate the Effect of Dapagliflozin in Combination With Baxdrostat Compared With Baxdrostat on Albuminuria in Participants With Chronic Kidney Disease and High Blood Pressure. (NCT07222917)

A Phase IIb, Randomised, Multicentre, Double-Blind Study to Evaluate the Effect of Baxdrostat in Combination With Dapagliflozin Compared With Baxdrostat on Albuminuria in Participants With Chronic Kidney Disease and High Blood Pressure.

🟒 Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: AstraZeneca

🩺 Plain-English Summary (8th-Grade Level)

International, Multicenter and Double-Blind study. The purpose is to measure the effect of baxdrostat in combination with dapagliflozin compared with baxdrostat/placebo on albuminuria, as well as safety, in participants with chronic kidney disease and high blood pressure.

Who can join: Review the eligibility criteria below.

Location: Research Site β€” Surprise, Arizona

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (71 Sites)

Showing the first 25 of 71 sites.

  • Research Site β€” Surprise, Arizona
  • Research Site β€” Hollywood, Florida
  • Research Site β€” Port Charlotte, Florida
  • Research Site β€” Port Orange, Florida
  • Research Site β€” Atlanta, Georgia
  • Research Site β€” Champaign, Illinois
  • Research Site β€” Wichita, Kansas
  • Research Site β€” Eatontown, New Jersey
  • Research Site β€” Greenville, North Carolina
  • Research Site β€” Jacksonville, North Carolina
  • Research Site β€” New Bern, North Carolina
  • Research Site β€” Columbus, Ohio
  • Research Site β€” Media, Pennsylvania
  • Research Site β€” East Providence, Rhode Island
  • Research Site β€” Arlington, Texas
  • Research Site β€” Pasadena, Texas
  • Research Site β€” San Antonio, Texas
  • Research Site β€” Woodbridge, Virginia
  • Research Site β€” Buenos Aires,
  • Research Site β€” Ciudad de Buenos Aires,
  • Research Site β€” Mar del Plata,
  • Research Site β€” Rosario,
  • Research Site β€” San NicolΓ‘s,
  • Research Site β€” Pernik,
  • Research Site β€” Plovdiv,

πŸ“ž Contact the Study Coordinator

Phone: (877) 240-9479

Email: information.center@astrazeneca.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—