🏛️ Verified NIH Record • Updated 2025-06-25

Safety, Pharmacokinetics, and Efficacy of AT 1501 in Patients Undergoing Kidney Transplant (NCT05027906)

A Phase 1b, Multicenter, Open Label Study to Evaluate the Safety, Pharmacokinetics and Efficacy of AT 1501 in Patients Undergoing Kidney Transplant

🟢 Recruiting Phase1 / Phase2 💊 Investigational Drug / Biologic Sponsor: Eledon Pharmaceuticals

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

This study will evaluate the safety, PK, and efficacy of AT 1501 in patients undergoing kidney transplantation.

Who can join: Review the eligibility criteria below.

Location: University of Cincinnati — Cincinnati, Ohio

Age range: 18 Years to 100 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (9 Sites)

  • University of Cincinnati — Cincinnati, Ohio
  • Royal Prince Alfred Hospital — Camperdown, New South Wales
  • Royal Adelaide Hospital — Adelaide, South Australia
  • Fundação Oswaldo Ramos - Hospital do Rim — São Paulo,
  • Providence Health Care - St. Paul's Hospital — Vancouver, British Columbia
  • Vancouver General Hospital — Vancouver, British Columbia
  • McGill University Health Care Centre — Montreal, Quebec
  • Liverpool University Hospitals NHS Foundation Trust - Royal Liverpool University Hospital — Liverpool,
  • Oxford University Hospitals NHS Foundation Trust - John Radcliffe Hospital — Oxford,

📞 Contact the Study Coordinator

Phone: (949) 238-8090

Email: clinicaltrials@eledon.com

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

💰 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 § 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.

💡 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.
🏛️ View Official NIH Record ↗