๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-30

Immunotherapy in Combination With Prednisone and Sirolimus for Kidney Transplant Recipients With Unresectable or Metastatic Skin Cancer (NCT05896839)

A Phase 2 Study of Nivolumab and Ipilimumab in Combination With Sirolimus and Prednisone in Kidney Transplant Recipients With Selected Unresectable or Metastatic Cutaneous Cancers

๐ŸŸข Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase II trial tests the combination of nivolumab and ipilimumab with sirolimus and prednisone for the treatment of skin (cutaneous) cancer that cannot be removed by surgery (unresectable) or that has spread from where it first started to other places in the body (metastatic) in kidney transplant recipients. Immunotherapy with nivolumab and ipilimumab, may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. Sirolimus and prednisone are immunosuppressants that are given to keep the body from rejecting the transplanted kidney. Giving nivolumab and ipilimumab in combination with sirolimus and prednisone may kill more cancer cells, while also keeping the transplanted kidney healthy, in patients with unresectable or metastatic cutaneous cancer who have received a kidney transplant.

Who can join: Review the eligibility criteria below.

Location: UC San Diego Moores Cancer Center โ€” La Jolla, California

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

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

๐Ÿ“ All Participating Trial Locations (26 Sites)

Showing the first 25 of 26 sites.

  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • Keck Medicine of USC Koreatown โ€” Los Angeles, California
  • Los Angeles General Medical Center โ€” Los Angeles, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Sibley Memorial Hospital โ€” Washington D.C., District of Columbia
  • UM Sylvester Comprehensive Cancer Center at Aventura โ€” Aventura, Florida
  • UM Sylvester Comprehensive Cancer Center at Coral Gables โ€” Coral Gables, Florida
  • UM Sylvester Comprehensive Cancer Center at Deerfield Beach โ€” Deerfield Beach, Florida
  • University of Miami Miller School of Medicine-Sylvester Cancer Center โ€” Miami, Florida
  • UM Sylvester Comprehensive Cancer Center at Kendall โ€” Miami, Florida
  • University of Miami Sylvester Comprehensive Cancer Center at Sole Mia โ€” North Miami, Florida
  • UM Sylvester Comprehensive Cancer Center at Plantation โ€” Plantation, Florida
  • Emory University Hospital/Winship Cancer Institute โ€” Atlanta, Georgia
  • Northwestern University โ€” Chicago, Illinois
  • Memorial Hospital East โ€” Shiloh, Illinois
  • University of Kentucky/Markey Cancer Center โ€” Lexington, Kentucky
  • Johns Hopkins University/Sidney Kimmel Cancer Center โ€” Baltimore, Maryland
  • Siteman Cancer Center at Saint Peters Hospital โ€” City of Saint Peters, Missouri
  • Siteman Cancer Center at West County Hospital โ€” Creve Coeur, Missouri
  • Washington University School of Medicine โ€” St Louis, Missouri
  • Siteman Cancer Center-South County โ€” St Louis, Missouri
  • Siteman Cancer Center at Christian Hospital โ€” St Louis, Missouri
  • NYU Langone Hospital - Long Island โ€” Mineola, New York
  • Laura and Isaac Perlmutter Cancer Center at NYU Langone โ€” New York, New York
  • UPMC Hillman Cancer Center โ€” Pittsburgh, Pennsylvania

๐Ÿ“ž Contact the Study Coordinator

Phone: (858) 822-5354

Email: cancercto@ucsd.edu

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

๐Ÿ’ฐ 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 ยง 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.

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—