- 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 6 of 6.
EudraCT Number: 2012-003147-30 | Sponsor Protocol Number: 1103-CT02 | Start Date*: 2012-11-20 | |||||||||||
Sponsor Name:Antisense Therapeutics Ltd | |||||||||||||
Full Title: A Phase II Randomised, Open-Label, Parallel Group Study of the Safety, Tolerability, Pharmacokinetics and Efficacy of Two Subcutaneous Dosing Regimens of ATL1103 in Adult Patients with Acromegaly. | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011128-70 | Sponsor Protocol Number: CSOM230G2304 | Start Date*: 2011-08-24 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, multicentre, phase III study to evaluate the efficacy and safety of pasireotide LAR in patients with Cushing’s disease | |||||||||||||
Medical condition: Cushing's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) NL (Completed) BE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000297-72 | Sponsor Protocol Number: 2-55-52030-727 | Start Date*: 2007-04-24 | |||||||||||
Sponsor Name:BEAUFOUR IPSEN Pharma | |||||||||||||
Full Title: Phase III, multicentre, open study to assess the efficacy and safety profiles of the co-administration of lanreotide Autogel 120 mg (administered via deep subcutaneous injections every 28 days) and... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GR (Completed) DE (Completed) CZ (Completed) DK (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024165-44 | Sponsor Protocol Number: CSOM230B2406 | Start Date*: 2011-08-05 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label, multi-center, expanded access study of pasireotide s.c. in patients with Cushing’s disease (Seascape) | |||||||||||||
Medical condition: Cushing’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Prematurely Ended) ES (Completed) CZ (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006182-88 | Sponsor Protocol Number: CRAD001CDE16 | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single arm, multicenter, single-stage phase II trial of RAD001 in Advanced and Metastatic Silent neuro-Endocrine Tumours in Europe | |||||||||||||
Medical condition: Patients with histologically confirmed advanced (unresectable or metastatic) non syndromic NET from foregut, midgut and hindgut, with exclusion of pancreatic NET, who have progressed within 12 mont... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) GB (Completed) ES (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005222-30 | Sponsor Protocol Number: LANHD01-2012 | Start Date*: 2013-02-04 | |||||||||||
Sponsor Name:UNIVERSITA' DI GENOVA | |||||||||||||
Full Title: Feasibility study to assess safety of high dose of lanreotide in net patients poorly controlled by standard doses of SSA | |||||||||||||
Medical condition: Neuroendocrine tumours | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003594-41 | Sponsor Protocol Number: CSOM230c2401 | Start Date*: 2008-11-26 | |||||||||||
Sponsor Name:Uppsala University Hospital, Dept of Medical Scienses | |||||||||||||
Full Title: An open label, multi-centre study of pasireotide LAR in addition to chemotherapy in patients with non-functioning, endocrine pancreatic tumors | |||||||||||||
Medical condition: Non-functioning endocrine pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005517-20 | Sponsor Protocol Number: IRST 100 01 | Start Date*: 2008-01-10 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
Full Title: Receptor radionuclide therapy with [177Lu- DOTA]0,Tyr3-octreotate (177Lu-DOTATATE): a phase II trial. | |||||||||||||
Medical condition: cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005202-10 | Sponsor Protocol Number: IEO388 | Start Date*: 2016-07-06 | ||||||||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | ||||||||||||||||||
Full Title: An open label, single-center, not controlled, exploratory study to develop and evaluate the application of a new technique of radioguided surgery in gastro-entero-pancreatic neuroendocrine tumors (... | ||||||||||||||||||
Medical condition: Gastro-entero-pancreatic neuroendocrine tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
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: 2013-001807-35 | Sponsor Protocol Number: S-20120206 | Start Date*: 2013-08-22 | |||||||||||
Sponsor Name:Department of Nuclear Medicine, Odense University Hospital | |||||||||||||
Full Title: Imaging with 111In-Octreotide SPECT-CT compared to 68Ga-DOTATATE PET-CT in patients admitted for evaluation of GastroEnteroPancreatic NeuroEndocrine Tumours, GEP-NETs | |||||||||||||
Medical condition: GastroEnteroPancreatic NeuroEndocrine Tumours (GEP-NET's) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012376-27 | Sponsor Protocol Number: ALADIN II | Start Date*: 2009-11-16 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: EFFECTS OF LONG-ACTING SOMATOSTATIN ON DISEASE PROGRESSION IN PATIENTS WITH AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND MODERATE/SEVERE RENAL INSUFFICIENCY(ALADIN II STUDY) | |||||||||||||
Medical condition: Polycystic Kidney | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023895-26 | Sponsor Protocol Number: CH-PHT-01 | Start Date*: 2011-04-15 | ||||||||||||||||
Sponsor Name:Chiasma, Inc. | ||||||||||||||||||
Full Title: Estudio de prueba de concepto diseñado para evaluar los efectos de Octreolin sobre el gradiente de presión venosa hepática en sujetos con cirrosis e hipertensión portal | ||||||||||||||||||
Medical condition: Cirrosis con signos de hipertensión portal significativa | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003067-38 | Sponsor Protocol Number: IRST100.17 | Start Date*: 2016-03-16 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | |||||||||||||
Full Title: 177Lutethium - Peptide Receptor Radionuclide Therapy (Lu-PRRT) plus Capecitabine versus Lu-PRRT in FDG positive, gastro-entero-pancreatic neuroendocrine tumors: a randomized phase II study. (Lu-Ca-S) | |||||||||||||
Medical condition: gastro-entero-pancreatic neuroendocrine tumors (GEP-NET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004186-83 | Sponsor Protocol Number: RZ358-606 | Start Date*: 2017-04-11 | ||||||||||||||||||||||||||
Sponsor Name:Rezolute, Inc. | ||||||||||||||||||||||||||||
Full Title: An Open-Label Multiple-Dose Study of RZ358 in Patients with Congenital Hyperinsulinism | ||||||||||||||||||||||||||||
Medical condition: Hypoglycemia associated with congenital hyperinsulinism | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) BG (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004992-62 | Sponsor Protocol Number: A-US-52030-328 | Start Date*: 2016-11-14 | |||||||||||
Sponsor Name:Ipsen Biopharmaceuticals, Inc | |||||||||||||
Full Title: A PHASE 3, PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, MULTI-CENTER, STUDY OF THE EFFICACY AND SAFETY OF LANREOTIDE AUTOGEL/ DEPOT 120 MG PLUS BSC VS. PLACEBO PLUS BSC FOR TUMOR CONTROL IN SUBJECTS WITH... | |||||||||||||
Medical condition: Lung Neuroendocrine Tumours | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) NL (Completed) DK (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001973-15 | Sponsor Protocol Number: SAFA-2-2014 | Start Date*: 2014-11-18 | ||||||||||||||||
Sponsor Name:University Clinic in Nephrology and Hypertension, Department of Medical Research | ||||||||||||||||||
Full Title: Renal Handling of Water and Sodium in Autosomal Dominant Polycystic Kidney Disease. The effects of tolvaptan on renal handling of water and sodium , vasoactive hormones and central hemodynamics dur... | ||||||||||||||||||
Medical condition: Hyponatreamia SIADH ( Syndrome of Inappropriate Antidiuretic Hormone Secretion) Overhydration Autosomal dominant polycystic kidney disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003418-10 | Sponsor Protocol Number: IRST202.02 | Start Date*: 2014-12-17 | ||||||||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI IRST - IRCCS | ||||||||||||||||||
Full Title: PEPTIDE RECEPTOR RADIONUCLIDE THERAPY WITH 90Y-DOTATOC IN RELAPSED/REFRACTORY DIFFUSE LARGE B CELL AND MANTLE CELL LYMPHOMAS | ||||||||||||||||||
Medical condition: Relapsed or refractory DLBCL (DIFFUSE LARGE B CELL LYMPHOMAS) or MCL (MANTLE CELL LYMPHOMAS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002133-37 | Sponsor Protocol Number: COR-2012-01 | Start Date*: 2014-11-17 | |||||||||||
Sponsor Name:Cortendo AB | |||||||||||||
Full Title: An Open Label Study to Assess the Safety and Efficacy of COR—003 (2S, 4R-Ketoconazole) in the Treatment of Endogenous Cushing’s Syndrome | |||||||||||||
Medical condition: Endogenous Cushing's syndrome (CS) or Cushing's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) BE (Completed) NL (Completed) SE (Completed) DK (Completed) DE (Completed) IT (Completed) BG (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001467-39 | Sponsor Protocol Number: GETNE1509 | Start Date*: 2015-07-24 | ||||||||||||||||
Sponsor Name:GETNE (Grupo Español de Tumores Neuroendocrinos) | ||||||||||||||||||
Full Title: A phase II study to evaluate the safety and efficacy of lenvatinib in patients with advanced grade 1/2 neuroendocrine neoplasmas of pancreatic and extrapancreatic origin. | ||||||||||||||||||
Medical condition: Patients with advanced/metastatic, histologically confirmed, grade 1/2 (G1/G2) of 2010 WHO classification neuroendocrine tumors of the pancreas after progression to a previous targeted agent (cohor... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) AT (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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