- Trials with a EudraCT protocol (2,303)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
2,303 result(s) found for: Oophorectomy.
Displaying page 5 of 116.
EudraCT Number: 2016-004151-79 | Sponsor Protocol Number: TRIO030 | Start Date*: 2017-05-08 | |||||||||||
Sponsor Name:Translational Research in Oncology (TRIO) | |||||||||||||
Full Title: A Presurgical Tissue-Acquisition Study to Evaluate Molecular Alterations in Human Breast Cancer Tissue Following Short-Term Exposure to the Androgen Receptor Antagonist Darolutamide (ODM-201) | |||||||||||||
Medical condition: Early Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001769-26 | Sponsor Protocol Number: MB02-C-02-17 | Start Date*: 2017-11-30 | |||||||||||
Sponsor Name:mAbxience Research SL | |||||||||||||
Full Title: STELLA – A Randomized, Multicenter, Multinational, Double-Blind Study to Assess the Efficacy and Safety of MB02 (Bevacizumab Biosimilar Drug) Versus Avastin® in Combination With Carboplatin and Pac... | |||||||||||||
Medical condition: Stage IIIB/IV Non-squamous Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) GR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016523-61 | Sponsor Protocol Number: PJMR0062105 | Start Date*: 2009-12-07 | |||||||||||
Sponsor Name:King’s College London [...] | |||||||||||||
Full Title: 18F-fluoride PET for Early Non-invasive Assessment of Cortical Bone Formation | |||||||||||||
Medical condition: Osteopenia Please note this is not a study to investigate the use of the IMP for the treatment of osteopenia but rather to validate a non-invasive imaging technique for measuring early changes in b... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001849-13 | Sponsor Protocol Number: 2013/cardio3 | Start Date*: 2013-07-09 |
Sponsor Name:ASLTO2-Maria Vittoria Hospital Cardiology | ||
Full Title: AnakInRa Treatment of Recurrent Idiopathic Pericarditis | ||
Medical condition: idiopathic recurrent pericarditis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000638-35 | Sponsor Protocol Number: CZOL446N2312 | Start Date*: 2004-09-15 |
Sponsor Name:Novartis Sverige AB | ||
Full Title: A 2-year randomized, multicenter, double-blind, placebocontrolled study to determine the efficacy and safety of intravenous zoledronic acid 5 mg administered either annually at randomization and 12... | ||
Medical condition: Postmenopausal Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002418-12 | Sponsor Protocol Number: CFEM345D2407 | Start Date*: 2005-01-25 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open-label, randomized, multicenter safety study to evaluate the skeletal and lipid profile effects of letrozole and tamoxifen in postmenopausal women with resected, receptor positive early brea... | ||
Medical condition: Bone loss attributed to cessation of ovarian estrogen production is common in postmenopausal women. In postmenopausal women with breast cancer, treatment with an aromatase inhibitor may further red... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005241-38 | Sponsor Protocol Number: LX6171.1-201-AAMI | Start Date*: 2007-11-12 | |||||||||||
Sponsor Name:Lexicon Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Determine Safety and Tolerability of LX6171 Oral Suspension Dosed for 28 Days in Subjects Exhibiting Age Associated Memory Impairment (AAMI) ... | |||||||||||||
Medical condition: Age-Associated Memory Impairment (AAMI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003078-41 | Sponsor Protocol Number: MUC-2/16 | Start Date*: 2018-11-23 |
Sponsor Name:MUCOS Pharma CZ s.r.o. | ||
Full Title: Reduction of post-traumatic systemic inflammatory response by Phlogenzym® using total hip replacement as a model. | ||
Medical condition: Total hip replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-003183-13 | Sponsor Protocol Number: OLATRA | Start Date*: 2018-05-25 | |||||||||||
Sponsor Name:GEICO - Grupo Español de Investigación en Cáncer de Ovario | |||||||||||||
Full Title: Phase-II study of olaparib as maintenance therapy after response to trabectedinpegylated liposomal doxorubicin in recurrent ovarian carcinoma. | |||||||||||||
Medical condition: Ovarian Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002825-52 | Sponsor Protocol Number: CRAD001A2401T | Start Date*: 2014-04-03 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: Single-center, open-label, single-arm Phase IIa study in kidney transplant patients with acute T-cell-mediated rejection in renal transplant according to Banff criteria (class IA and IB) without (s... | |||||||||||||
Medical condition: Acute cellular rejection after kidney transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002767-98 | Sponsor Protocol Number: UCDCRC/19/01 | Start Date*: 2020-05-28 | |||||||||||
Sponsor Name:University College Dublin | |||||||||||||
Full Title: A Pilot Study of Combined Immune Checkpoint Inhibition in combination with ablative therapies in Subjects with Hepatocellular Carcinoma (HCC) | |||||||||||||
Medical condition: Patients with Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004575-12 | Sponsor Protocol Number: DOMEC | Start Date*: 2019-07-05 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: DOMEC - phase II trial of Durvalumab (MEDI4736) and Olaparib in Metastatic/recurrent Endometrial Cancer, a DGOG trial. | ||
Medical condition: advanced endometrial cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004230-37 | Sponsor Protocol Number: BCX7353-312 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: An open-label study to provide berotralstat access to subjects with type 1 and 2 hereditary angioedema who were previously enrolled in berotralstat studies | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001976-39 | Sponsor Protocol Number: GORTEC-2018-02 | Start Date*: 2018-12-14 | |||||||||||
Sponsor Name:GORTEC | |||||||||||||
Full Title: A phase II trial of radiotherapy-durvalumab without prophylactic neck irradiation in squamous cell carcinoma of the head and neck | |||||||||||||
Medical condition: Untreated Squamous cell carcinoma : Oral cavity, oropharynx, hypopharynx or larynx | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002687-65 | Sponsor Protocol Number: 2317 | Start Date*: 2019-04-18 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: The NUVOLA TRIAL: Neoadjuvant chemoteraphy in Unresectable oVarian cancer with OLAparib and weekly carboplatin plus paclitaxel. A phase II open-label multi-centre study. | |||||||||||||
Medical condition: ADVANCED OVARIAN CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001203-32 | Sponsor Protocol Number: DEDALUS | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:FONDAZIONE I.R.C.C.S. POLICLINICO SAN MATTEO | |||||||||||||
Full Title: An open-label, multi-center, phase 2 study of chemo-immunotherapy followed by reduced-dose hypo-fractionated RT and maintenance immunotherapy for stage III unresectable Non –small-cell lung carcino... | |||||||||||||
Medical condition: stage III unresectable non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000230-35 | Sponsor Protocol Number: 014-FPO18 | Start Date*: 2018-10-17 | |||||||||||
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
Full Title: Phase II study on the combination of trabectedin and olaparib for advanced, platinum-resistant ovarian/tubes and primary of peritoneum cancer. - TROOPS trial (TRabectedin plus Olaparib in advanced ... | |||||||||||||
Medical condition: platinum-resistant ovarian carcinoma or Fallopian tubes or primary of peritoneum | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000617-20 | Sponsor Protocol Number: MITO31 | Start Date*: 2018-11-14 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
Full Title: A phase II trial of Olaparib in patients with recurrent ovarian cancer wild type for germline and somatic BRCA 1 and 2 genes: The MITO 31 transalational study. | |||||||||||||
Medical condition: patients with recurrent ovarian cancer wild type for germline and somatic BRCA 1 and 2 genes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004758-39 | Sponsor Protocol Number: ESR-18-13485 | Start Date*: 2019-06-12 | |||||||||||
Sponsor Name:AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA | |||||||||||||
Full Title: A PHASE II STUDY OF CAPECITABINE PLUS CONCOMITANT RADIATION THERAPY FOLLOWED BY DURVALUMAB (MEDI4736) AS PREOPERATIVE TREATMENT IN RECTAL CANCER | |||||||||||||
Medical condition: Locally advanced (T3-4 N0-1) rectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002855-12 | Sponsor Protocol Number: RM-493-034 | Start Date*: 2022-04-22 |
Sponsor Name:Rhythm Pharmaceuticals Inc. | ||
Full Title: A 2-Stage (Open-Label Run-in followed by Randomized Withdrawal), Double-Blind, Placebo-Controlled, Phase 2 study of Setmelanotide in Patients with Specific Gene Defects in the Melanocortin-4 Rece... | ||
Medical condition: Specific Gene Defects in the Melanocortin-4 Receptor Pathway, responsible for improper functions of certain messenger materials in the body. E.g Melanocyte-Stimulating Hormone (MSH) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) DE (Completed) ES (Ongoing) NL (Completed) GR (Completed) | ||
Trial results: View results |
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