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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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,
π 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.
π° 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.
More studies in Neuroendocrine Tumors
- Targeted Alpha-emitter Therapy of PRRT NaΓ―ve and Previous PRRT Neuroendocrine Tumor Patients β Denver, Colorado
- Lu-DOTATATE Treatment in Patients With 68Ga-DOTATATE Somatostatin Receptor Positive Neuroendocrine Tumors β Hamilton, Ontario
- A Safety Study of 212Pb-VMT-alpha-NET in Patients With Neuroendocrine Tumors β Iowa City, Iowa
- Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients β Gilbert, Arizona
- Lesion-to-lesion Comparison of 68Ga-HA-DOTATATE, 18F-DOPA, and 18F-FDG PET/CT in the Evaluation of Metastatic Neuroendocrine Tumors β Edmonton, Alberta
Explore by condition: All Neuroendocrine Tumors clinical trials
π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.