Radioactive drug safety tracked for years in rare cancer patients
NCT ID NCT05017662
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study follows 20 people with neuroendocrine tumors who previously received a radioactive drug called 177Lu-satoreotide tetraxetan. Researchers check for long-term side effects, including new cancers, every 3 months for up to 5 years. The goal is to understand the drug's safety over time, not to test if it works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 177Lu-satoreotide tetraxetan (a radioactive drug)
- What this could lead to
- If successful, this study will provide crucial safety data that could support the future use of this treatment for neuroendocrine tumors.
- What could go wrong
- This is a small, observational follow-up study with only 20 participants, so results may not apply to all patients. It does not test whether the treatment works, only its long-term safety.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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20 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Apr 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participant is capable of giving signed informed consent * Participant must have received at least one infusion of 177Lu-IPN01072 in Study OPS-C-001 Exclusion Criteria: \- There are no exclusion criteria in this safety surveillance study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Aarhus University Hospital
Aarhus, 8200, Denmark
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Hôtel Dieu de Nantes
Nantes, 44093 Cedex 1, France
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Medical University of Vienna
Vienna, 1090, Austria
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Peter Maccallum Cancer Center
Melbourne, 3002, Australia
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Ramsay Hollywood Private Hospital
Perth, 6009, Australia
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Royal Free Hospital London
London, NW3 2QG, United Kingdom
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University Hospital Basel
Basel, 4031, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Swiss registry aims to map rare neuroendocrine tumors
- Can patients drop monthly injections after targeted radiotherapy for neuroendocrine tumors?
- Can a vast image library unlock better pancreatic diagnoses?
- Can a sharper PET tracer light up hidden neuroendocrine tumors?
- Can patient records reveal who will respond to neuroendocrine tumor treatments?
- Can a new drug formulation shrink Hard-to-Treat neuroendocrine tumors?