- Trials with a EudraCT protocol (77)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
77 result(s) found for: Adrenal tumor.
Displaying page 1 of 4.
| EudraCT Number: 2004-001125-20 | Sponsor Protocol Number: FIRM-ACT | Start Date*: 2004-07-26 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
| Full Title: First International Randomized trial in Metastatic Adrenocortical Cancer Treatment FIRM-ACT Etoposide, Doxorubicin, Cisplatin and Mitotane vs. Streptozotocin and Mitotane | |||||||||||||
| Medical condition: Chemotherapy in patients with locally advanced or metastatic adrenocortical cancer in adults and children | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001802-27 | Sponsor Protocol Number: F002MH0218_1 | Start Date*: 2019-04-16 | ||||||||||||||||||||||||||
| Sponsor Name:University Hospital Wuerzburg | ||||||||||||||||||||||||||||
| Full Title: A Multicenter, Open-label, Phase II Study to Evaluate the Efficacy and Safety of Cabozantinib in Advanced (Unresectable or Metastatic) Adrenocortical Carcinoma. | ||||||||||||||||||||||||||||
| Medical condition: Advanced (Unresectable or Metastatic) Adrenocortical Carcinoma | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-002632-99 | Sponsor Protocol Number: ONC-NET-01 | Start Date*: 2011-10-14 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: SUTNET Trial: Biological and Clinical Phase II study of Sunitinib in patients with unresectable and/or metastatic pheochromocytoma/paraganglioma | |||||||||||||
| Medical condition: Patients with unresectable and/or metastatic pheochromocytomas/paragangliomas | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001591-35 | Sponsor Protocol Number: ASST-ONCO-CABAC2017 | Start Date*: 2017-12-27 | |||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: Multicenter, prospective, non-randomized, phase II trial designed to evaluate the activity of Cabazitaxel in patients with advanced Adreno-Cortical- Carcinoma progressing after previous chemotherap... | |||||||||||||
| Medical condition: Histologically confirmed diagnosis of ACC Locally advanced or metastatic disease not amenable to radical surgery resection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000494-91 | Sponsor Protocol Number: PEMBR-01 | Start Date*: 2022-12-22 | |||||||||||
| Sponsor Name:Narodowy Instytut Onkologii im. Marii Skłodowskiej-Curie, Państwowy Instytut Badawczy | |||||||||||||
| Full Title: A multicentre, open-label phase 2 study to evaluate the efficacy and safety of pembrolizumab in the treatment of advanced, progressive adrenocortical carcinoma. | |||||||||||||
| Medical condition: carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004530-38 | Sponsor Protocol Number: ASSTBS-FARONCO-PESETA-20 | Start Date*: 2022-05-30 | |||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: PROSPECTIVE, PHASE II STUDY TO EVALUATE THE EFFICACY OF ADDITION OF PROGESTERONE TO STANDARD CHEMOTHERAPY ACCORDING TO EDP SCHEME PLUS MITOTANE IN PATIENTS WITH ADVANCED ADRENALCORTICAL (PESETA TRIAL) | |||||||||||||
| Medical condition: advanced/ metastatic patients with ACC | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000580-90 | Sponsor Protocol Number: ASSTBS-ONCO-ACACIA-18 | Start Date*: 2018-06-20 | |||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: Multicenter randomized open-label phase III trial of Adjuvant Chemotherapy vs. observation or mitotane after primary surgical resection of localized | |||||||||||||
| Medical condition: localized Adrenocortical CarcInomA with high risk of recurrence | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-000115-10 | Sponsor Protocol Number: SPON CU 086 | Start Date*: 2005-10-14 |
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised, double blind, placebo-controlled, cross-over study of the effects of dehydroepiandrosterone replacement on vascular function in patients with primary and secondary adrenal insufficiency. | ||
| Medical condition: Primary and secondary adrenal failure | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022417-25 | Sponsor Protocol Number: NL 33608 | Start Date*: 2011-04-18 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: Pheochromocytoma RandomisEd Study Comparing adRenoreceptor Inhibiting agents for Preoperative Treatment | |||||||||||||
| Medical condition: Perioperative hemodynamic control in patients undergoing resection of a pheochromocytoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005157-24 | Sponsor Protocol Number: 75688 | Start Date*: 2021-09-21 | |||||||||||
| Sponsor Name:UMC Utrecht | |||||||||||||
| Full Title: [18F]mFBG PET-CT imaging of pheochromocytoma | |||||||||||||
| Medical condition: Pheochromocytoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000748-32 | Sponsor Protocol Number: SPI-62-CL-2002 | Start Date*: 2023-08-29 | |||||||||||
| Sponsor Name:Sparrow Pharmaceuticals, Inc. | |||||||||||||
| Full Title: SPI-62 as a Treatment for Hypercortisolism Related to a Benign Adrenal Tumor | |||||||||||||
| Medical condition: Hypercortisolism Related to a Benign Adrenal Tumor | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003163-29 | Sponsor Protocol Number: SNIPP | Start Date*: 2012-06-08 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: SNIPP study - A investigator initiated phase II study of Sunitinib in patients with recurrent paraganglioma/pheochromocytoma | |||||||||||||
| Medical condition: Paraganglioma/pheochromocytoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006824-20 | Sponsor Protocol Number: CSOM230BDE02 | Start Date*: 2007-11-08 | |||||||||||
| Sponsor Name:Universitätsklinikum Essen - Zentrum für Innere Medizin - Klinik für Endokrinologie | |||||||||||||
| Full Title: Monocenter, double blinded, exploratory, randomized, study investigating the influence of Pasireotide on the hormonal activity of Pheochromocytoma – proof of concept study | |||||||||||||
| Medical condition: Pheochromocytoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003396-19 | Sponsor Protocol Number: EOADR1-19 | Start Date*: 2020-05-28 | |||||||||||||||||||||
| Sponsor Name:Enterome | |||||||||||||||||||||||
| Full Title: A phase 1/2 trial of EO2401, a novel microbial-derived peptide therapeutic vaccine, in combination with PD-1 check point blockade, for treatment of patients with locally advanced or metastatic adr... | |||||||||||||||||||||||
| Medical condition: - locally advanced or metastatic adrenocortical carcinoma (ACC) - malignant pheochromocytoma/paraganglioma (MPP) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Completed) NL (Ongoing) ES (Completed) DE (Completed) DK (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-002873-47 | Sponsor Protocol Number: SOGUG2011-03 | Start Date*: 2011-11-25 | |||||||||||
| Sponsor Name:Grupo Español de Oncología Genitourinaria (SOGUG) | |||||||||||||
| Full Title: PHASE II CLINICAL TRIAL OF DOVITINIB (TKI-258) IN FIRST-LINE METASTATIC OR LOCALLY ADVANCED NON-RESECTABLE ADRENOCORTICAL CARCINOMA | |||||||||||||
| Medical condition: Carcinoma adrenocortical metastásico o localmente avanzado no resecable, confirmado histológicamente. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002211-11 | Sponsor Protocol Number: MIP-IB12 | Start Date*: 2008-02-13 | |||||||||||
| Sponsor Name:Molecular Insight Pharmaceuticals, Inc | |||||||||||||
| Full Title: A PHASE I-II STUDY EVALUATING THE MAXIMUM TOLERATED DOSE, DOSIMETRY, SAFETY, AND EFFICACY OF ULTRATRACE™ IOBENGUANE I 131 IN PATIENTS WITH MALIGNANT PHEOCHROMOCYTOMA/PARAGANGLIOMA | |||||||||||||
| Medical condition: MALIGNANT PHEOCHROMOCYTOMA/PARAGANGLIOMA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004076-34 | Sponsor Protocol Number: 7487-CL-0209 | Start Date*: 2014-02-27 | ||||||||||||||||||||||||||
| Sponsor Name:Astellas Pharma Global Development, Inc. | ||||||||||||||||||||||||||||
| Full Title: A phase II open-label rollover study for subjects that have participated in an Astellas sponsored linsitinib trial | ||||||||||||||||||||||||||||
| Medical condition: Solid tumors | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2013-003431-29 | Sponsor Protocol Number: CBGG492A2216 | Start Date*: 2014-05-27 |
| Sponsor Name:Novartis Farma S.p.A. | ||
| Full Title: A multicenter medical safety follow-up study for patients with partial onset seizures who received more than 28 days of total exposure to BGG492 in studies CBGG492A2207 and/or CBGG492A2212. | ||
| Medical condition: Testing for adrenal cortical adenomas in male and female patients Testing for uterine endometrial stromal sarcromas in all female patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000864-82 | Sponsor Protocol Number: hydrocortisone | Start Date*: 2011-12-22 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: A randomized double blind cross-over study of the effects of low dose and high dose hydrocortisone replacement therapy on cognition, quality of life, metabolic profile and somatosensation in patien... | |||||||||||||
| Medical condition: Secondary adrenal insufficiency | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (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 (Trial now transitioned) PT (Prematurely Ended) PL (Trial now transitioned) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
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