Carcinoma, NeuroendocrinePhase 2NCT01876771
A Trial to Assess the Safety and Effectiveness of Lutetium-177 Octreotate Therapy in Neuroendocrine Tumours
A Phase 2 study testing [177]Lu-DOTA-TATE in people with Carcinoma, Neuroendocrine, run by AHS Cancer Control Alberta at 1 site in Canada.
Trial summary
Neuroendocrine tumours (NETs) are rare, slow growing, and diagnosis is often delayed with advanced metastases at presentation. In select patient populations, radioisotope therapy with Lutetium-177 (Lu-DOTA-TATE) has been shown to be a safe and effective palliative therapy, and has been widely used by research groups… Read more about this study
- Who is it for?
- Ages 14 to 90 years
- Conditions the study is for
- Carcinoma, Neuroendocrine
- What is being tested?
- [177]Lu-DOTA-TATE
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 413 participants
- Where
- 1 siteCanada
- Study dates
- 29 Apr 2014to Dec 2042
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 to 90 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Group A (Primary Therapy) Inclusion Criteria:
- Male or female ≥ 14 - 90 years of age.
- At least 1 tumour site reliably evaluable by CT or magnetic resonance imaging (MRI) of at least 1.0 cm (smallest dimension) or ≥ 1.5 cm lymph node disease (smallest dimension) (the target lesion) within 26 weeks of enrolment, with documented presence of somatostatin receptors on radionuclide imaging, with uptake greater than liver background as assessed by planar Octreoscan® images or Ga-68 labelled somatostatin analogue (68Ga-DOTATATE or 68Ga-HA-DOTATATE) PET imaging (or other available somatostatin receptor targeting PET agents) obtained within 1 year of enrolment. Patients with bone-only disease can be enrolled provided there is presence of somatostatin receptor positive tumour(s) on radionuclide imaging corresponding to osteolytic or osteoblastic bone lesions on CT or MRI, with uptake greater than liver background as assessed by planar Ocgtreoscan(R) images or somatostatin receptor PET imaging regardless of size.
- Histologically confirmed diagnosis of neuroendocrine tumor.
- Progressive disease documented by anatomic imaging and/or presence of new lesions on somatostatin receptor imaging assessed by comparable studies. In the opinion of the investigator, patients with no progression on imaging may still be considered eligible in presence of carcinoid symptoms refractory to treatment with somatostatin receptor analogues or functional Pheochromocytoma/Paraganglioma symptoms that are not well controlled with current medical treatment.
- 18F-FDG PET/CT whole-body imaging within 26 weeks of enrolment.
- Life expectancy greater than 12 weeks from enrollment.
- Serum creatinine ≤ 150 µmol/L, and a calculated (Cockcroft-Gault) or estimated GFR of ≥ 50 mL/min measured within 2 weeks of enrollment.
- Haemoglobin concentration ≥ 90 g/L; white blood cell (WBC) count ≥ 2 x 10^9/L; platelets ≥ 100 x 10^9/L measured within 2 weeks of enrolment.
- Liver function tests (total bilirubin, alanine transaminase (ALT), aspartate transaminase (AST)) ≤ 3X the limit of normal measured within 2 weeks of enrolment. Serum albumin ≥ 23 g/L within 2 weeks of enrolment.
- Eastern Cooperative Oncology Group (ECOG) Performance Scale Score ≤ 2 measured within 2 weeks of enrolment.
- Provide written informed consent prior to enrolment.
Group B (Maintenance Therapy) Inclusion Criteria:
- Male or female ≥ 14 - 90 years of age.
- Have previously received Lu-DOTA-TATE treatment under the SAP.
- Life expectancy greater than 12 weeks from enrolment.
- Serum creatinine ≤ 150 μmol/L, and a calculated (Cockcroft-Gault) or estimated glomerular filtration rate (GFR) of ≥ 50 mL/min measured within 2 weeks of enrolment.
- Haemoglobin concentration ≥ 90 g/L; white blood cell (WBC) count ≥ 2 x 10^9/L; platelets ≥ 100 x 10^9/L measured within 2 weeks of enrolment.
- Liver function tests (total bilirubin, alanine transaminase (ALT), aspartate transaminase (AST)) ≤ 3X the limit of normal measured within 2 weeks of enrolment. Serum albumin ≥ 23 g/L within 2 weeks of enrolment.
- Eastern Cooperative Oncology Group (ECOG) Performance Scale Score ≤ 2 measured within 2 weeks of enrolment.
- Provide written informed consent prior to enrolment.
Group A (Primary Therapy) Exclusion Criteria:
- Have previously received Lu-DOTA-TATE therapy.
- Potential for surgery with curative intent. Local surgery for symptomatic relief permitted as long as target lesion unaffected.
- Major surgery within 12 weeks of enrolment. Minor surgeries such as removal of superficial skin lesions, laser eye surgery, cataract surgery, laparoscopic procedures and other procedures that are minimally invasive are permitted at the Investigator's discretion.
- Liver embolization [transcatheter arterial embolization (TAE), TACE, or TARE] within 4 weeks of enrolment.
- Radioisotope therapy within 12 weeks of enrolment.
- Systemic therapy: mTOR inhibitors and tyrosine kinase inhibitors within 6 weeks of enrolment; chemotherapy and interferon within 8 weeks of enrolment.
- Change in long-acting somatostatin analogues, dosage, or dosage frequency within 12 weeks of enrolment unless changes are required to manage uncontrolled symptoms.
- Localized external beam irradiation with target lesion(s) in the radiation field. Other localized external beam therapy is permitted.
- Known brain metastases unless these metastases have been treated and stabilized (confirmed by CT) for ≥ 4 months prior to enrolment
- Uncontrolled diabetes mellitus defined as random glucose ≥ 2X the upper limit of normal (or HbA1c > 10%, if results available) within 12 weeks of enrolment.
- Another significant medical, psychiatric or surgical condition uncontrolled by treatment, which may interfere with completion or conduct of the study (such as urinary incontinence, co-existing malignancies).
- Pregnancy.
- Breast feeding.
- Prior radiation therapy to more than 25% of the bone marrow.
- If, in the opinion of the investigator, other treatments are considered more appropriate than the investigational therapy, based on patient and disease characteristics.
- Known allergy to somatostatin analogues or any components of the study medication.
Group B (Maintenance Therapy) Exclusion Criteria:
- Another significant medical, psychiatric or surgical condition uncontrolled by treatment, which may interfere with completion or conduct of the study (such as urinary incontinence or co-existing malignancies).
- Pregnancy.
- Breast feeding.
- Known allergy to somatostatin analogues or any components of the study medication.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: An Open-label Phase II Study of Lutetium-177 [DOTA0, Tyr3] Octreotate (Lu-DOTA-TATE) Treatment in Patients With Somatostatin Receptor Positive Tumours
Neuroendocrine tumours (NETs) are rare, slow growing, and diagnosis is often delayed with advanced metastases at presentation. In select patient populations, radioisotope therapy with Lutetium-177 (Lu-DOTA-TATE) has been shown to be a safe and effective palliative therapy, and has been widely used by research groups in Europe. A brand of Lu-DOTA-TATE (Lutathera(R)) is approved for the treatment of gastroenteropancreatic NETs in Europe, the U.S., and more recently in Canada. While Lutathera(R) is approved in Canada, it is not publicly funded in Alberta. Lu-DOTA-TATE has been used at the Cross Cancer Institute to treat more than 300 patients with NETs since August, 2010. Our Lu-DOTA-TATE treatment was initially given under Health Canada's Special Access Programme (SAP), with each individual treatment requiring separate approval. In 2014, Health Canada requested we conduct a clinical trial with Lu-DOTA-TATE instead.
The purpose of this study is to: 1) assess the efficacy of Lu-DOTA-TATE treatment in patients with somatostatin receptor positive tumours; 2) assess the safety of Lu-DOTA-TATE; 3) assess the effect of Lu-DOTA-TATE on Quality of Life and survival.
Read the detailed description
The proposed clinical trial will be a Phase II, open label, single site study in subjects with somatostatin receptor positive tumours. Radioactive Lu-DOTA-TATE doses are fixed within a range of 1.85 - 5.55 GBq ± 10%, with individual doses based on specified risk factors. There will be two groups of subjects enrolled in this study. Group A subjects (primary therapy) will have progressive somatostatin receptor positive tumours and have never received Lu-DOTA-TATE. Group B subjects (maintenance therapy) will be those subjects who have previously received Lu-DOTA-TATE under the Special Access Programme (SAP) and will maintain their treatment schedule when they are entered into the study.
All subjects in Group A will be treated in an induction stage using 10-14 week dosing for up to 4 treatments. If an individual patient shows stable or improving disease status with no significant toxicities after the 4 induction treatments, they will be assessed 12-20 weeks after the last therapeutic treatment for entry into the maintenance stage. Patients will be re-assessed for stable or improving disease status with no significant toxicities 12-20 weeks after every other treatment of the maintenance stage for consideration of further maintenance treatments (re-evaluations), up to a maximum of 8 treatments per patient if there have been no significant toxicities or progression. At each treatment, an amino acid solution is infused prior to and during the Lu-DOTA-TATE infusion to protect the kidneys. Subjects will be followed for 6 months and 1 year (± 4 weeks) following their last treatment dose to determine progression-free survival, and annually (± 4 weeks) for up to 5 years following their last treatment dose to determine overall survival. All subjects meeting evaluation criteria will be analysed for safety, and all Group A subjects who have received at least two treatments of Lu-DOTA-TATE will be evaluated for efficacy. Those Group B subjects with adequate baseline data for comparison collected retrospectively from a chart review study (REV-LUT-001) may also be evaluated for safety and efficacy. Additional optional characterization of tumour samples from subjects who have had surgery before or during the study may be performed to characterize NET tumour biology changes following Lu-DOTA-TATE treatment.
- Conditions
- Carcinoma, Neuroendocrine
- Being tested
- [177]Lu-DOTA-TATE
- Keywords
- 177lutetium-DOTA(O)Tyr3)octreotate
- Medical subject headings
- Carcinoma, Neuroendocrine
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
[177]Lu-DOTA-TATEDrug
Also called Lu-DOTA-TATE
Peptide receptor radionuclide therapy (PPRT)
| Study group | Role | What they receive |
|---|---|---|
| [177]Lu-DOTA-TATE Therapy | Experimental | Nominal, induction stage dose of 150 mCi (5.55 GBq) [177]Lu-DOTA-TATE every 10 - 14 weeks for 4 treatments.
Nominal maintenance stage dose of 100 mCi (3.7 GBq) [177]Lu-DOTA-TATE every 22 - 40 weeks, up to a maximum of 8 treatments. Receives: Drug: [177]Lu-DOTA-TATE |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Tumour response of the target lesion(s) through end of treatment
Tumor response of the target lesions(s) will be assessed by anatomic criteria in reference to RECIST 1.1 used in conjuction with lesion avidity on Nuclear Medicine scans, such as Lu-177 post-therapy scans, Octreoscan, [68]Ga-DOTATATE or [68]Ga-HA-DOTATATE PET, [18]F-FDG PET, [18]F-FDOPA PET, and/or others, as clinically indicated.
Measured: At screening, 12-20 weeks after each treatment cycle, and 6 months and 1 year after the last treatment
Median progression-free survival
Time from date of enrolment to the first documented target lesion progression or death due to any cause, which ever occurs first.
Measured: Up to 1 year after last treatment
Lu-177 scan disease evaluation
A post-therapy Lu-177 scan will be conducted up to 3 days after each Lu-DOTA-TATE treatment to determine the intensity of tumour uptake of Lu-DOTA-TATE and the extent of tumour burden. Changes in Lu-177 scan data will also be used to stratify tumour response.
Measured: Up to 3 days after each Lu-DOTA-TATE treatment
Change in tumour marker levels
As clinically indicated, serum Chromogranin-A, urinary 5-HIAA, metanephrines, and/or other tumour markers will be collected at baseline, at each re-evaluation, at end of treatment, and at 6 months and 1 year after the last treatment. Tumour marker parameters will be recorded and all changes will be summarized.
Measured: At baseline, 12-20 weeks after each treatment cycle, and 6 months and 1 year after last treatment
Secondary outcomes (8)
Number of participants with adverse events as a measure of safety and tolerability
All participants will be evaluated for AE occurence from treatment 1 up to 5 years after the last treatment.
Measured: Up to 5 years after last treatment
Change in haematology
Blood samples will be analyzed for hemoglobin, platelet count, white blood cell count, lymphocyte count, and neutrophil count to monitor and record clinically significant out of range values that are indicative of toxicity. Samples will be collected at screening, within 2 weeks prior to each treatment, 6 weeks after each treatment, at each re-evaluation (12-20 weeks after treatments 4, 6, 8, and 10) and at 6 months and 1 year after the last treatment. Changes will be analyzed using descriptive statistics, and any identified adverse events will be tabulated and categorized according to CTCAE v.4.
Measured: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment.
Change in renal function
Blood samples will be analyzed for creatinine in order to calculate the glomerular filtration rate (GFR) and monitor and record clinically significant out of range values that are indicative of toxicity. Samples will be collected at screening, within 2 weeks prior to each treatment, 6 weeks after each treatment, at each re-evaluation (12-20 weeks after treatments 4, 6, 8, and 10) and at 6 months and 1 year after the last treatment. Changes will be analyzed using descriptive statistics, and any identified adverse events will be tabulated and categorized according to CTCAE v.4.
Measured: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment
Change in liver function
Blood samples will be analyzed for total bilirubin, aspartate transaminase, and alanine transaminase to monitor and record clinically significant out of range values that are indicative of toxicity. Samples will be collected at screening, within 2 weeks prior to each treatment, 6 weeks after each treatment, at each re-evaluation (12-20 weeks after treatments 4, 6, 8, and 10) and at 6 months and 1 year after the last treatment. Changes will be analyzed using descriptive statistics, and any identified adverse events will be tabulated and categorized according to CTCAE v.4.
Measured: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment
Median, 1, 2, 3, 4, and 5-year overall survival
Time from date of enrolment to date of death due to any cause or date of censoring at the last time the participant was known to be alive.
Measured: Up to 5 years after last treatment
Change in Quality of Life (EORTC QLQ)
The European Organisation for Research Treatment of Cancer (EORTC) QLQ-C30 v.3 in conjunction with the supplementary module QLQ-GI.NET21 Quality of Life questionnaires will be administered prior to each treatment on the visit date. The core questionnaire and supplementary module will be scored according to the scoring manual, and changes analyzed to assess the effect of Lu-DOTA-TATE treatment on Quality of Life.
Measured: Prior to each treatment
Change in Quality of Life (ESAS-r)
The Edmonton Symptom Assessment System Revised (ESAS-r) will be administered prior to each treatment on visit date. The questionnaire will be scored according to the scoring manual, and changes analyzed to assess the effect of Lu-DOTA-TATE treatment on Quality of Life.
Measured: Prior to each treatment
Change in tumour biology (optional)
Subjects who have had surgery prior to or after Lu-DOTA-TATE therapy may have existing tumour tissue sample tested to characterize NET tumour biology and the effects of Lu-DOTA-TATE therapy on tumour cell function.
Measured: Up to 1 year after last treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Jun 2013 (estimated)
- Study start29 Apr 2014
- Primary completionDec 2042 (estimated)
- Study completionDec 2042 (estimated)
Why it stopped: Study closed to accrual given widespread availability of the similar marketed product, Lutathera(R), and the corresponding lack of accrual to the study.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Carcinoma, NeuroendocrineStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 413 participants (actual)
Sponsor and investigators
- Lead sponsor
- AHS Cancer Control Alberta
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Stella Koumna, MD, Principal investigator, Cross Cancer Institute, Cancer Care Alberta
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01876771
- Sponsor's protocol ID
- TX-LUT-001
- Other IDs
- HREBA.CC-18-0165
- Status last verified
- Jul 2026
- First submitted
- 10 Apr 2013
- Last updated
- 27 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-label Phase II Study of Lutetium-177 [DOTA0, Tyr3] Octreotate (Lu-DOTA-TATE) Treatment in Patients With Somatostatin Receptor Positive Tumours
- ClinicalTrials.gov ID
- NCT01876771
- Acronym / sponsor ID
- TX-LUT-001
- Conditions
- Carcinoma, Neuroendocrine
- Keywords
- 177lutetium-DOTA(O)Tyr3)octreotate
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- SuspendedReason stopped: Study closed to accrual given widespread availability of the similar marketed product, Lutathera(R), and the corresponding lack of accrual to the study.
- Enrolment
- 413 participants (actual)
- Lead sponsor
- AHS Cancer Control AlbertaUniversity, hospital or other
- Study start
- 29 Apr 2014 (actual)
- Primary completion
- Dec 2042 (estimated)
- Study completion
- Dec 2042 (estimated)
- First posted
- 13 Jun 2013 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Neuroendocrine tumours (NETs) are rare, slow growing, and diagnosis is often delayed with advanced metastases at presentation. In select patient populations, radioisotope therapy with Lutetium-177 (Lu-DOTA-TATE) has been shown to be a safe and effective palliative therapy, and has been widely used by research groups in Europe. A brand of Lu-DOTA-TATE (Lutathera(R)) is approved for the treatment of gastroenteropancreatic NETs in Europe, the U.S., and more recently in Canada. While Lutathera(R) is approved in Canada, it is not publicly funded in Alberta. Lu-DOTA-TATE has been used at the Cross Cancer Institute to treat more than 300 patients with NETs since August, 2010. Our Lu-DOTA-TATE treatment was initially given under Health Canada's Special Access Programme (SAP), with each individual treatment requiring separate approval. In 2014, Health Canada requested we conduct a clinical trial with Lu-DOTA-TATE instead.
The purpose of this study is to: 1) assess the efficacy of Lu-DOTA-TATE treatment in patients with somatostatin receptor positive tumours; 2) assess the safety of Lu-DOTA-TATE; 3) assess the effect of Lu-DOTA-TATE on Quality of Life and survival.
Detailed description
The proposed clinical trial will be a Phase II, open label, single site study in subjects with somatostatin receptor positive tumours. Radioactive Lu-DOTA-TATE doses are fixed within a range of 1.85 - 5.55 GBq ± 10%, with individual doses based on specified risk factors. There will be two groups of subjects enrolled in this study. Group A subjects (primary therapy) will have progressive somatostatin receptor positive tumours and have never received Lu-DOTA-TATE. Group B subjects (maintenance therapy) will be those subjects who have previously received Lu-DOTA-TATE under the Special Access Programme (SAP) and will maintain their treatment schedule when they are entered into the study.
All subjects in Group A will be treated in an induction stage using 10-14 week dosing for up to 4 treatments. If an individual patient shows stable or improving disease status with no significant toxicities after the 4 induction treatments, they will be assessed 12-20 weeks after the last therapeutic treatment for entry into the maintenance stage. Patients will be re-assessed for stable or improving disease status with no significant toxicities 12-20 weeks after every other treatment of the maintenance stage for consideration of further maintenance treatments (re-evaluations), up to a maximum of 8 treatments per patient if there have been no significant toxicities or progression. At each treatment, an amino acid solution is infused prior to and during the Lu-DOTA-TATE infusion to protect the kidneys. Subjects will be followed for 6 months and 1 year (± 4 weeks) following their last treatment dose to determine progression-free survival, and annually (± 4 weeks) for up to 5 years following their last treatment dose to determine overall survival. All subjects meeting evaluation criteria will be analysed for safety, and all Group A subjects who have received at least two treatments of Lu-DOTA-TATE will be evaluated for efficacy. Those Group B subjects with adequate baseline data for comparison collected retrospectively from a chart review study (REV-LUT-001) may also be evaluated for safety and efficacy. Additional optional characterization of tumour samples from subjects who have had surgery before or during the study may be performed to characterize NET tumour biology changes following Lu-DOTA-TATE treatment.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| [177]Lu-DOTA-TATE Therapy | Experimental | Drug: [177]Lu-DOTA-TATENominal, induction stage dose of 150 mCi (5.55 GBq) [177]Lu-DOTA-TATE every 10 - 14 weeks for 4 treatments. Nominal maintenance stage dose of 100 mCi (3.7 GBq) [177]Lu-DOTA-TATE every 22 - 40 weeks, up to a maximum of 8 treatments. |
Who may qualify
- Ages
- 14 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| [177]Lu-DOTA-TATEAlso: Lu-DOTA-TATEPeptide receptor radionuclide therapy (PPRT) | Drug | [177]Lu-DOTA-TATE Therapy |
Primary outcome
Change in Tumour response of the target lesion(s) through end of treatment
Time frame: At screening, 12-20 weeks after each treatment cycle, and 6 months and 1 year after the last treatment
Tumor response of the target lesions(s) will be assessed by anatomic criteria in reference to RECIST 1.1 used in conjuction with lesion avidity on Nuclear Medicine scans, such as Lu-177 post-therapy scans, Octreoscan, [68]Ga-DOTATATE or [68]Ga-HA-DOTATATE PET, [18]F-FDG PET, [18]F-FDOPA PET, and/or others, as clinically indicated.
Median progression-free survival
Time frame: Up to 1 year after last treatment
Time from date of enrolment to the first documented target lesion progression or death due to any cause, which ever occurs first.
Lu-177 scan disease evaluation
Time frame: Up to 3 days after each Lu-DOTA-TATE treatment
A post-therapy Lu-177 scan will be conducted up to 3 days after each Lu-DOTA-TATE treatment to determine the intensity of tumour uptake of Lu-DOTA-TATE and the extent of tumour burden. Changes in Lu-177 scan data will also be used to stratify tumour response.
Change in tumour marker levels
Time frame: At baseline, 12-20 weeks after each treatment cycle, and 6 months and 1 year after last treatment
As clinically indicated, serum Chromogranin-A, urinary 5-HIAA, metanephrines, and/or other tumour markers will be collected at baseline, at each re-evaluation, at end of treatment, and at 6 months and 1 year after the last treatment. Tumour marker parameters will be recorded and all changes will be summarized.
8 secondary outcomes
Number of participants with adverse events as a measure of safety and tolerability
Time frame: Up to 5 years after last treatment
Change in haematology
Time frame: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment.
Change in renal function
Time frame: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment
Change in liver function
Time frame: At screening, within 2 weeks prior to at 6 weeks after each treatment, at each re-evaluation, and at 6 months and 1 year after last treatment
Median, 1, 2, 3, 4, and 5-year overall survival
Time frame: Up to 5 years after last treatment
Change in Quality of Life (EORTC QLQ)
Time frame: Prior to each treatment
Change in Quality of Life (ESAS-r)
Time frame: Prior to each treatment
Change in tumour biology (optional)
Time frame: Up to 1 year after last treatment
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Jul 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stella Koumna, MD principal investigator
Cross Cancer Institute, Cancer Care Alberta
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing [177]Lu-DOTA-TATE in people with Carcinoma, Neuroendocrine, run by AHS Cancer Control Alberta at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: paused, as of the sponsor's last update on 27 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Tumour response of the target lesion(s) through end of treatment (time frame: At screening, 12-20 weeks after each treatment cycle, and 6 months and 1 year after the last treatment). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jul 2026.