πŸ›οΈ Verified NIH Record β€’ Updated 2025-12-17

Post-Authorization Long-Term Safety Study of LUTATHERA (NCT03691064)

International, Non-interventional, Post-Authorization Long-Term Safety Study of Lutathera, in Patients With Unresectable or Metastatic, Well-Differentiated, Somatostatin Receptor Positive, Gastroenteropancreatic Neuroendocrine Tumours

πŸ”΅ Active, Not Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: Advanced Accelerator Applications

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

Study to assess the long-term safety of LUTATHERA for the labeled indication (SmPC/USPI).

Who can join: Review the eligibility criteria below.

Location: Banner MD Anderson Cancer Center β€” Phoenix, 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 (20 Sites)

  • Banner MD Anderson Cancer Center β€” Phoenix, Arizona
  • The Ohio State University Wexner Medical Center β€” Portland, Ohio
  • Oregon Health & Sciences University Hospital β€” Portland, Oregon
  • Virginia Mason in Seattle β€” Seattle, Washington
  • Novartis Investigative site β€” Clichy,
  • Novartis Investigative site β€” Lyon,
  • Novartis Investigative site β€” Villejuif,
  • Novartis Investigative site β€” Coimbra, Coimbra District
  • Novartis Investigative site β€” Santiago de Compostela, La Corunya
  • Novartis Investigative site β€” Majadahonda, Madrid
  • Novartis Investigative site β€” Birmingham,
  • Novartis Investigative site β€” Cambridge,
  • Novartis Investigative site β€” Glasgow,
  • Novartis Investigative site β€” Liverpool,
  • Novartis Investigative site β€” London,
  • Novartis Investigative site β€” London,
  • Novartis Investigative site β€” London,
  • Novartis Investigative site β€” London,
  • Novartis Investigative site β€” Manchester,
  • Novartis Investigative site β€” Sheffield,

πŸ“ž Contact the Study Coordinator

Phone: (877) 632-6789

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†—