- Trials with a EudraCT protocol (120)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
120 result(s) found for: Octreotide.
Displaying page 3 of 6.
EudraCT Number: 2021-000598-95 | Sponsor Protocol Number: HS-20-674 | Start Date*: 2021-07-30 | |||||||||||
Sponsor Name:Camurus AB | |||||||||||||
Full Title: A Phase 2, randomized, double-blind, placebo-controlled, multi-center trial to assess the efficacy and safety of octreotide subcutaneous depot (CAM2029) in patients with acute respiratory distress ... | |||||||||||||
Medical condition: Acute respiratory distress syndrome (ARDS) caused by COVID-19 or other disorders | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000507-12 | Sponsor Protocol Number: RYZ101-301 | Start Date*: 2023-06-12 | ||||||||||||||||
Sponsor Name:RayzeBio, Inc. | ||||||||||||||||||
Full Title: Phase 1b/3 global, randomized, controlled, open-label trial comparing treatment with RYZ101 to standard of care (SoC) therapy in subjects with inoperable, advanced, somatostatin receptor expressing... | ||||||||||||||||||
Medical condition: gastro-enteropancreatic neuroendocrine tumors (GEP-NETs) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) NL (Trial now transitioned) BE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001833-42 | Sponsor Protocol Number: CRN00808-02 | Start Date*: 2018-11-13 | |||||||||||
Sponsor Name:Crinetics Pharmaceuticals, Inc. | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized withdrawal study to evaluate the safety, pharmacokinetics and efficacy of CRN00808 in patients with acromegaly that are responders to octreotide LAR o... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) GR (Completed) PL (Completed) GB (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006097-76 | Sponsor Protocol Number: LOTUS | Start Date*: 2013-01-11 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: RANDOMIZED PHASE 3 TRIAL EVALUATING THE EFFICACY OF LOCOREGIONAL TREATMENT WITH TRANSARTERIAL EMBOLIZATION (TAE) FOR LIVER METASTASIS, IN COMBINATION WITH OCTREOTIDE LAR, IN PATIENTS WITH NEUROENDO... | |||||||||||||
Medical condition: PATIENTS WITH NEUROENDOCRINE TUMOR AND INOPERABLE LIVER METASTASIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
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 (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003963-58 | Sponsor Protocol Number: 5FLUOCT | Start Date*: 2005-03-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
Full Title: CONTINOUS INFUSION OF 5-FLUORURACIL PLUS OCTREOTIDE LONG ACTING IN PATIENTS WITH NEUROENDOCRINE ADVANCED NOT SMALL CELL TUMORS | |||||||||||||
Medical condition: TREATMENT OF PATIENTS WITH NON SMALL CELL NEUROENDOCRINE TUMORS WITH LOW PROLIFERATIVE ACTIVITY WITHOUT SURGICAL APPROACH | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004033-32 | Sponsor Protocol Number: RADIOMEN | Start Date*: 2013-12-13 |
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | ||
Full Title: AN OPEN, MONOCENTRIC, NOT CONTROLLED CLINICAL TRIAL TO DEVELOP AND EVALUATE THE CLINICAL APPLICATION OF A NEW BETA PROBE FOR RADIOGUIDED SURGERY IN MENINGIOMA TUMOR | ||
Medical condition: SUBJECTS WITH CONVEXITY MENINGIOMA TUMORS OF NEW DIAGNOSIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005642-37 | Sponsor Protocol Number: sandopouch-01 | Start Date*: 2007-04-10 |
Sponsor Name:University of Leuven, Division of Gastroenterology | ||
Full Title: Sandostatin® in the treatment of diarrhea in patients with ileal pouch anal anastomosis. | ||
Medical condition: IPAA Pouchitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005585-12 | Sponsor Protocol Number: 1 | Start Date*: 2007-12-20 | |||||||||||
Sponsor Name:Department of Internal Medicine of the University of Munich | |||||||||||||
Full Title: Prospektive, offene Studie zur Prüfung der Wirksamkeit der zusätzlichen Gabe des Somatostatinanalogon Octreotid (Sandostatin) bzw. des Dopaminagonisten Cabergolin (Dostinex) bei Patientin mit Akrom... | |||||||||||||
Medical condition: acromegaly (= growth hormone hypersecretion mostly caused by a pituitary adenoma) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001078-94 | Sponsor Protocol Number: 1981 | Start Date*: 2007-05-21 |
Sponsor Name:Radboud University medical centre | ||
Full Title: Treatment of dumping syndrome with Lanreotide Autogel | ||
Medical condition: treatment of the dumping syndrome with Lanreotide Autogel | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000888-41 | Sponsor Protocol Number: MetNET1trial | Start Date*: 2014-06-05 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei tumori | ||||||||||||||||||
Full Title: Activity and safety of Everolimus in combination with octreotide LAR and Metformin in patients with advanced pancreatic well-differentiated Neuroendocrine Tumors (pWDNETs): a Phase II, open, mono... | ||||||||||||||||||
Medical condition: advanced/ or not resectable well differnciated pancreatic neuroendocrin tumor | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004179-11 | Sponsor Protocol Number: 2018-4898 | Start Date*: 2019-06-03 |
Sponsor Name:Radboudumc | ||
Full Title: Effectiveness of Somatostatin Analogues in Patients with hereditary hemorrhagic telangiectasia and symptomatic gastrointestinal bleeding, the SAIPAN-trial: a multicenter, randomized, open-label, pa... | ||
Medical condition: Hereditary hemorrhagic telangiectasia (HHT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Ongoing) FR (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023674-39 | Sponsor Protocol Number: AKRO1 | Start Date*: 2014-08-05 | |||||||||||
Sponsor Name:Österreichisches Akromegalie Register | |||||||||||||
Full Title: Evaluation of a standardized treatment regimen for acromegaly: A multi centre intervention study | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016722-13 | Sponsor Protocol Number: CSOM230C2402 | Start Date*: 2010-06-10 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase III, multicenter, randomized, parallel-group study to assess the efficacy and safety of double-blind pasireotide LAR 40 mg and pasireotide LAR 60 mg versus open-label octreotide LAR or lanr... | |||||||||||||
Medical condition: Acromegaly is characterized by chronic hypersecretion of growth hormone (GH), clinical features comprise structural and functional changes occurring in practically all organs. Cardiovascular diseas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) IT (Completed) NO (Completed) BE (Completed) DE (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019066-92 | Sponsor Protocol Number: 2-55-52030-730/TR321 | Start Date*: 2010-08-31 | |||||||||||
Sponsor Name:Ipsen Pharma SAS | |||||||||||||
Full Title: A double-blind, randomized placebo-controlled clinical trial investigating the efficacy and safety of Somatuline Depot (lanreotide) Injection in the treatment of carcinoid syndrome | |||||||||||||
Medical condition: Carcinoid syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LV (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004507-18 | Sponsor Protocol Number: CRAD001C2325 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter phase III study in patients with advanced carcinoid tumor receiving Sandostatin LAR® Depot and RAD001 10 mg/d or Sandostatin LAR® Depot a... | |||||||||||||
Medical condition: Low grade neuroendocrine carcinoma consists of carcinoid and pancreatic endocrine tumors. These tumors originate from the neuroendocrine cells throughout the body and are capable of producing vario... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SE (Completed) FR (Completed) BE (Completed) SK (Completed) DE (Completed) ES (Completed) NL (Completed) GB (Completed) GR (Completed) IT (Completed) FI (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002630-31 | Sponsor Protocol Number: CSOM230C2413 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase IIIb multicenter, open-label, single arm study to evaluate the efficacy and safety of pasireotide in patients with acromegaly inadequately controlled with first generation somatostatin ana... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) PT (Completed) IT (Completed) FR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004707-12 | Sponsor Protocol Number: CRAD001C2X01B | Start Date*: 2013-05-16 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open-label, multi-center everolimus roll-over protocol for patients who have completed a previous Novartis-sponsored everolimus study and are judged by the investigator to benefit from continued... | ||
Medical condition: Disease corresponding to the Novartis-sponsored study the patient will be transitioning from | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) NL (Prematurely Ended) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005376-17 | Sponsor Protocol Number: 201401 | Start Date*: 2014-06-20 | |||||||||||
Sponsor Name:Erasmus Medical Center | |||||||||||||
Full Title: Sandostatin therapy in sarcoidosis | |||||||||||||
Medical condition: Sarcoidosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003444-53 | Sponsor Protocol Number: CSMS995BIT12 | Start Date*: 2005-10-11 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A randomised, open label, multicenter study comparing the efficacy and safety of medical treatment with Sandostatin LAR 30 mg administered every 21 days for 6 months with that of Sandostatin LAR 60... | |||||||||||||
Medical condition: Treatment of acromegalic patients partially responsive to somatostatin analogues | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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