- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
61 result(s) found for: Somatostatin Receptor.
Displaying page 1 of 4.
EudraCT Number: 2016-005129-35 | Sponsor Protocol Number: FENET-2016 | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI FERRARA | |||||||||||||
Full Title: "Peptide Receptor Radionuclide Therapy (PRRT) with somatostatin analogs in tumors over-expressing somatostatin receptors" | |||||||||||||
Medical condition: Tumors over-expressing somatostatin receptors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006889-29 | Sponsor Protocol Number: MEC-2008-322 | Start Date*: 2009-02-25 |
Sponsor Name:ErasmusMC | ||
Full Title: A pilotstudy comparing systemic versus locoregional injection of radiolabelled somatostatin analogues in patients with neuroendocrine Gastro-Entero_Pancreatic (GEP) tumors. | ||
Medical condition: Uptake of Octreoscan in sst-2 receptor positive Gastro Entero Pancreatic neuroendocrine tumors injected in systemical and locoregional way. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001562-15 | Sponsor Protocol Number: CAAA601A22301 | Start Date*: 2019-11-15 | |||||||||||||||||||||
Sponsor Name:Advanced Accelerator Applications SA | |||||||||||||||||||||||
Full Title: This is a multicenter, stratified, randomized, open-label comparator-controlled, Phase III study in patients with somatostatin receptor positive, well-differentiated G2 and G3, advanced GEP NETs, d... | |||||||||||||||||||||||
Medical condition: Patients with somatostatin receptor positive, well-differentiated G2 and G3, advanced GEP NETs | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) DE (Ongoing) NL (Ongoing) ES (Ongoing) IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002960-42 | Sponsor Protocol Number: Yttrium-90-02 | Start Date*: 2017-11-15 | |||||||||||
Sponsor Name:AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA | |||||||||||||
Full Title: 173/5000 Forse cercavi: Terapia radiometabolica recettoriale-mediata con [90Y-DOTA0-Tyr3]-octreotide (90Y-DOTATOC) nei tumori endocrini del tratto gastroenteropancreatico e bronchiale. (Yttrium-90... | |||||||||||||
Medical condition: Patients with Somatostatin receptors Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005545-20 | Sponsor Protocol Number: IJBNMDOCASTOR | Start Date*: 2014-12-23 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: The CaStOR study Carcinoid Tumors after failure of Somatostatin analogs: a randomized phase III of Octreotide Lutate Peptid Receptor radionuclide Therapy (PRRT) versus inteRferon α-2b | |||||||||||||
Medical condition: Progressive, unresectable, non-pancreatic gastrointestinal neuroendocrine tumors resistant to therapy with somatostatin analogues. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002230-20 | Sponsor Protocol Number: CRN00808-03 | Start Date*: 2018-11-13 | |||||||||||
Sponsor Name:Crinetics Pharmaceuticals, Inc. | |||||||||||||
Full Title: An open label exploratory study to evaluate the safety, pharmacokinetics and efficacy of CRN00808 in patients with acromegaly treated with somatostatin analogue based treatment regimens (ACROBAT EDGE) | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) DE (Completed) GR (Completed) PL (Completed) GB (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004091-35 | Sponsor Protocol Number: EMC-NET1 | Start Date*: 2019-04-19 | |||||||||||||||||||||
Sponsor Name:Erasmus University Medical Center | |||||||||||||||||||||||
Full Title: Improving Treatment Options for Somatostatin Type 2 Receptor Negative Neuroendocrine Tumor Patients | |||||||||||||||||||||||
Medical condition: Neuroendocrine tumors | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000549-15 | Sponsor Protocol Number: S63678 | Start Date*: 2020-08-05 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Al18F-NOTA-octreotide PET imaging of the somatostatin receptor in neuroendocrine tumors | ||
Medical condition: Neuroendocrine tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005546-63 | Sponsor Protocol Number: DOTATER1_26_15 | Start Date*: 2016-05-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE SANTA MARIA NUOVA/IRCCS DI REGGIO EMILIA | |||||||||||||
Full Title: Peptide receptor radionuclide therapy in tumors with high expression of somatostatine receptors. | |||||||||||||
Medical condition: Cancer patients with high expression of somatostatin receptors (neurendocrine tumors, thyroid tumors, lung tumors, meningiomas). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000849-40 | Sponsor Protocol Number: HS-19-657 | Start Date*: 2021-08-23 | ||||||||||||||||
Sponsor Name:Camurus AB | ||||||||||||||||||
Full Title: A randomized, multi-center, open-label, active-controlled Phase 3 trial to assess the efficacy and safety of octreotide subcutaneous depot (CAM2029) versus octreotide LAR or lanreotide ATG in patie... | ||||||||||||||||||
Medical condition: gastroenteropancreatic neuroendocrine tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) BE (Trial now transitioned) HU (Ongoing) DE (Ongoing) NL (Trial now transitioned) IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005049-11 | Sponsor Protocol Number: AAA-III-01 | Start Date*: 2012-04-25 | ||||||||||||||||
Sponsor Name:Advanced Accelerator Applications | ||||||||||||||||||
Full Title: A multi-centre, stratified, open, randomized, comparator-controlled, parallel-group phase III study comparing treatment with 177Lu-DOTA0-Tyr3-Octreotate to Octreotide LAR in patients with inoperabl... | ||||||||||||||||||
Medical condition: Patients with inoperable, progressive, OctreoScan® positive, well-differentiated neuroendocrine tumours of the small bowel (midgut carcinoid tumours), who are treated with 20 mg or 30 mg Octreotide... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) IT (Completed) BE (Completed) PT (Completed) FR (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002951-39 | Sponsor Protocol Number: CAAA601A32201 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
Sponsor Name:Advanced Accelerator Applications SA | |||||||||||||||||||||||||||||||||
Full Title: A multicenter open-label study to evaluate safety and dosimetry of Lutathera in adolescent patients with somatostatin receptor positive gastroenteropancreatic neuroendocrine (GEP-NET) tumors, pheoc... | |||||||||||||||||||||||||||||||||
Medical condition: somatostatin receptor positive gastroenteropancreatic neuroendocrine (GEP-NET) tumors, pheochromocytoma and paragangliomas | |||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) FR (Ongoing) PT (Ongoing) PL (Ongoing) BE (Completed) IT (Ongoing) NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001468-12 | Sponsor Protocol Number: PEN-221-001 | Start Date*: 2017-01-16 |
Sponsor Name:Tarveda Therapeutics, Inc. | ||
Full Title: A Phase 1/2a, open-label multicenter study to assess the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of PEN-221 in patients with somatostatin receptor 2 expressing ad... | ||
Medical condition: Somatostatin receptor 2 (SSTR2) expressing advanced cancers, including gastroenteropancreatic (GEP) cancer or lung cancer or thymus cancer or other NETs (Neuroendocrine tumour) or small cell lung c... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001108-35 | Sponsor Protocol Number: NRA 6290010 | Start Date*: 2006-07-03 | |||||||||||
Sponsor Name:Clinic of University of Wuerzburg | |||||||||||||
Full Title: CHANGES OF LEFT VENTRICULAR MASS AND CARDIAC FUNCTION IN PATIENTS WITH ACTIVE ACROMEGALY DURING TREATMENT WITH THE GROWTH HORMONE RECEPTOR ANTAGONIST PEGVISOMANT: AN OPEN-LABELLED, PROSPECTIVE STUDY | |||||||||||||
Medical condition: Somavert (Pegvisomant) is approved for the treatment of acromegalic patients who have had an inadequate response to surgery and/or radiation therapy and/or other medical therapy as Somatostatin Ana... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012260-14 | Sponsor Protocol Number: 20050418 | Start Date*: 2010-08-27 |
Sponsor Name:Department of Endocrine Oncology | ||
Full Title: An open, non-randomized phase-2 study of efficacy and safety of treatment with 177Lutetium-DOTA0-Tyr3-octreotate in patients with neuroendocrine tumors | ||
Medical condition: Patients with malignant neuroendocrine tumours, not amenable to surgical treatment or radiofrequency ablation. Renal, bone marrow and liver function must be sufficient. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005431-70 | Sponsor Protocol Number: CRN00808-09 | Start Date*: 2022-03-04 | |||||||||||
Sponsor Name:Crinetics Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Controlled, Multi-Center Study to Evaluate the Safety and Efficacy of Paltusotine in Subjects with Acromegaly Treated with Long-acting Somatostatin Receptor Ligands | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) AT (Completed) DE (Completed) HU (Ongoing) PL (Ongoing) BG (Ongoing) ES (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004377-99 | Sponsor Protocol Number: CSMS995ADE17-RNOP-11/B-01 | Start Date*: 2007-04-17 |
Sponsor Name:Medizinische Einrichtungen des Bezirks Oberpfalz GmbH | ||
Full Title: Phase I study of Somatostatin-Analogues as Second Line Treatment in Adult Patients with Recurrent Medulloblastoma (WHO IV) | ||
Medical condition: patients with medulloblastoma in whom therapy for primary disease (minimum: best possible resection, radiotherapy and one chemotherapy regimen) failed | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003167-38 | Sponsor Protocol Number: NL50643.09r.r4 | Start Date*: 2015-04-28 |
Sponsor Name:Radboudumc | ||
Full Title: 68Ga-NODAGA-exendin-4 PET/CT in patients with AHH - a prospective comparative evaluation of preoperative imaging Under the FP7 project Betacure (602812); Personalized diagnosis and treatment of hy... | ||
Medical condition: Adult endogenous hyperinsulinemic hypoglycemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-006068-99 | Sponsor Protocol Number: DuoNen2020 | Start Date*: 2021-09-20 |
Sponsor Name:Narodowe Centrum Badań Jądrowych, Ośrodek Radioizotopów POLATOM | ||
Full Title: Tandem therapy LutaPol/ItraPol (177Lu / 90Y-DOTATATE) as an effective method in the treatment of neuroendocrine neoplasms, Acronym: DuoNen, 2019 / ABM / 01/00077 | ||
Medical condition: Diagnosed and confirmed histopathologically disseminated or locally unresectable, well and moderately differentiated (G1 and G2) neuroendocrine neoplasms of the gastrointestinal tract (GEP-NET) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001897-13 | Sponsor Protocol Number: ITM-LET-01 | Start Date*: 2017-08-22 | |||||||||||
Sponsor Name:ITM Solucin GmbH | |||||||||||||
Full Title: A prospective, randomised, Controlled, Open-label, Multicentre phase III study to evaluate efficacy and safety of Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-Edotreotide compared to tar... | |||||||||||||
Medical condition: Patients with inoperable, progressive, somatostatin receptor-positive(SSTR+), neuroendocrine tumours of gastroenteric or pancreatic origin (GEP-NET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) AT (Ongoing) GB (GB - no longer in EU/EEA) NL (Ongoing) PL (Ongoing) CZ (Ongoing) BE (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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