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

Nivolumab and Multi-fraction Stereotactic Radiosurgery With or Without Ipilimumab in Treating Patients With Recurrent Grade II-III Meningioma (NCT03604978)

A Phase I/II Study of Nivolumab Plus or Minus Ipilimumab in Combination With Multi-Fraction Stereotactic Radiosurgery for Recurrent High-Grade Radiation-Relapsed Meningioma

๐Ÿ”ต Active, Not Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

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

This phase I/II trial studies the side effects and best dose of nivolumab when given together with multi-fraction stereotactic radiosurgery and to see how well they work with or without ipilimumab in treating patients with grade II-III meningioma that has come back (recurrent). Immunotherapy with monoclonal antibodies, such as nivolumab and ipilimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Stereotactic radiosurgery is a specialized radiation therapy that delivers a single, high dose of radiation directly to the tumor and may cause less damage to normal tissue. Giving nivolumab and multi-fraction stereotactic radiosurgery with or without ipilimumab may work better in treating patients with grade II-III meningioma.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

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 (29 Sites)

Showing the first 25 of 29 sites.

  • Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona
  • City of Hope Comprehensive Cancer Center โ€” Duarte, California
  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • Los Angeles General Medical Center โ€” Los Angeles, California
  • USC / Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • UC Irvine Health/Chao Family Comprehensive Cancer Center โ€” Orange, California
  • UCHealth University of Colorado Hospital โ€” Aurora, Colorado
  • 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
  • Mayo Clinic in Florida โ€” Jacksonville, Florida
  • University of Miami Miller School of Medicine-Sylvester Cancer Center โ€” Miami, Florida
  • UM Sylvester Comprehensive Cancer Center at Kendall โ€” Miami, Florida
  • UM Sylvester Comprehensive Cancer Center at Plantation โ€” Plantation, Florida
  • University of Kansas Cancer Center โ€” Kansas City, Kansas
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • Johns Hopkins University/Sidney Kimmel Cancer Center โ€” Baltimore, Maryland
  • Mayo Clinic in Rochester โ€” Rochester, Minnesota
  • Siteman Cancer Center at West County Hospital โ€” Creve Coeur, Missouri
  • Washington University School of Medicine โ€” St Louis, Missouri
  • University of Nebraska Medical Center โ€” Omaha, Nebraska
  • Laura and Isaac Perlmutter Cancer Center at NYU Langone โ€” New York, New York
  • NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center โ€” New York, New York
  • UNC Lineberger Comprehensive Cancer Center โ€” Chapel Hill, North Carolina
  • Duke University Medical Center โ€” Durham, North Carolina

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

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†—