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NCT04727723Completed

Italian Prospective Observational Study Assessing the Effectiveness and Outcomes Associated With Lutathera Treatment in GEP-NETs

Two Steps Italian Prospective obsErvationAL Study Assessing the Effectiveness and Outcomes Associated With LUtathera (177Lu) Oxodotreotide Treatment in Adult Subjects With Unresectable or Metastatic, Progressive, Well Differentiated (G1 and G2), Somatostatin Receptor Positive Gastroenteropancreatic-neuroendocrine Tumours (GEP-NETs) - REAL-LU

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

This is a multicentre long-term non-interventional study of adult subjects diagnosed with unresectable or metastatic, progressive, well differentiated (G1 and G2), somatostatin receptor positive GEP-NETs who have been prescribed Lutathera® in standard clinical practice.

Status (registry)
Completed
Study type
Observational
Enrollment
164 (actual)
First submitted
20 Nov 2020
Start date
9 Mar 2021
Primary completion date
10 Mar 2026
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT04727723

What you commit to

  • Study type: Observational
  • Participants enrolled: 164
  • From 9 Mar 2021 to the primary completion date, 10 Mar 2026
  • 18 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in a current or prior investigational study within 30 days preceding enrolment or within 5 half-lives of the investigational product, whichever is longer.

Who the study is looking for

  • Written informed consent must be obtained prior to any data collection.
  • Patients must be diagnosed with unresectable or metastatic, progressive, well differentiated (G1 and G2), somatostatin receptor positive gastroenteropancreatic-neuroendocrine tumour (GEP-NET).
  • Aged ≥18 years.
  • Patients must be naïve to treatment with Lutathera® at enrolment.

Age in the registry: 18 years to 100 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
Coordinator of this site? Confirm its status
AlessandriaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
BolognaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
BresciaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
ConaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
FlorenceItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
LatinaItalyUnknown status
Novartis Investigative Site
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MeldolaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
MessinaItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
MilanItalyUnknown status
Novartis Investigative Site
Coordinator of this site? Confirm its status
NaplesItalyUnknown status
Novartis Investigative Site
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NegrarItalyUnknown status
Novartis Investigative Site
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PadovaItalyUnknown status
Novartis Investigative Site
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PisaItalyUnknown status
Novartis Investigative Site
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Reggio EmiliaItalyUnknown status
Novartis Investigative Site
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Rionero in VoltureItalyUnknown status
Novartis Investigative Site
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RomaItalyUnknown status
Novartis Investigative Site
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RozzanoItalyUnknown status
Novartis Investigative Site
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TorinoItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.