- Trials with a EudraCT protocol (730)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
730 result(s) found for: Ovarian Cancer.
Displaying page 19 of 37.
EudraCT Number: 2007-003323-20 | Sponsor Protocol Number: CP4055-204 | Start Date*: 2008-05-30 |
Sponsor Name:Clavis Pharma ASA | ||
Full Title: A Phase I/II Study of CP-4055 in Patients with Platinum Resistant Ovarian Cancer | ||
Medical condition: A phase I/II clinical study of CP4055 in patients with platinum resistant ovarian cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000418-23 | Sponsor Protocol Number: AGO/2015/002 | Start Date*: 2015-12-18 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Intraoperative intraperitoneal chemoperfusion to treat peritoneal minimal residual disease in stage III ovarian cancer: a randomized phase II trial. | ||
Medical condition: stage III ovarian cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005208-20 | Sponsor Protocol Number: 2019DEPO-TRIGGER001 | Start Date*: 2022-08-10 | |||||||||||
Sponsor Name:Universitair Ziekenhuis Brussel | |||||||||||||
Full Title: Depo-Trigger trial: GnRH agonist DEPOt TRIGGER for final oocyte maturation in breast cancer patients undergoing fertility preservation: a pilot study. | |||||||||||||
Medical condition: Female patients with breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003475-42 | Sponsor Protocol Number: GTAEXS617-001 | Start Date*: 2023-05-23 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Exscientia AI Ltd | ||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2 open-label multicenter study to assess the safety, pharmacokinetics, and anti-tumor activity of GTAEXS617 in patients with advanced solid tumors. | ||||||||||||||||||||||||||||||||||||||
Medical condition: advanced solid tumors | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004323-20 | Sponsor Protocol Number: BNT211-01 | Start Date*: 2020-06-30 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:BioNTech Cell & Gene Therapies GmbH | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase 1/2a, first-in-human, open-label, dose escalation trial with expansion cohorts to evaluate safety and preliminary efficacy of CLDN6 CAR-T with or without CLDN6 RNA-LPX in patients with CLDN6-... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: CLDN6-positive relapsed or refractory advanced solid tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004780-13 | Sponsor Protocol Number: CeNturIOn-2016 | Start Date*: 2018-08-22 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: An open-label, randomised, phase II trial of ruCaparib combined with Nivolumab +/- Ipilimumab to augment response in homologous repair deficient patients with relapsed Ovarian, primary peritoneal a... | |||||||||||||
Medical condition: High grade serous ovarian cancer (includes histologically identical fallopian tube and primary peritoneal cancers and high grade G3 endometrioid histological subtypes) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005024-14 | Sponsor Protocol Number: ARD6122 | Start Date*: 2006-03-28 |
Sponsor Name:Sanofi-Synthélabo Recherche, a subsidiary of sanofi-aventis group | ||
Full Title: Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos y en dos fases, de la eficacia y seguridad de AVE0005 (VEGF Trap) administrado por vía intravenosa cada 2 semanas en pacientes ... | ||
Medical condition: pacientes con cáncer de ovario avanzado resistente a platino y resistente a topotecano y/o doxorubicina liposomal. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) SE (Completed) PT (Completed) DE (Completed) HU (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003128-35 | Sponsor Protocol Number: GETHI-2013-01 | Start Date*: 2014-06-05 | |||||||||||
Sponsor Name:Grupo Español de Tumores Huérfanos e Infrecuentes (GETHI) | |||||||||||||
Full Title: Open label phase II clinical trial of Orteronel (TAK-700) in metastatic or advanced non-resectable granulosa cell ovarian tumors. The Greko II study. | |||||||||||||
Medical condition: Metastatic or advanced non-resectable granulosa cell ovarian tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002616-22 | Sponsor Protocol Number: CHORINE | Start Date*: 2012-05-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Stage IIIC unresectable epithelial ovarian/tubal cancer with partial or complete response after 1st line neoadjuvant chemotherapy (3 cycles CBDCA+Paclitaxel): a phase 3 prospective randomized stu... | |||||||||||||
Medical condition: EPITHELIAL OVARIAN/TUBAL CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006227-17 | Sponsor Protocol Number: D8410C00001 | Start Date*: 2022-09-14 | |||||||||||||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||
Full Title: A Modular Phase I/IIa, Open-label, Multi-centre Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Ascending Doses of AZD9574 as Monotherapy an... | |||||||||||||||||||||||||||||||||
Medical condition: Module 1: advanced/relapsed ovarian, breast, pancreatic or prostate cancer where patients loss of function or predicted loss of function mutation in BRCA1, BRCA2, PALB2, RAD51C, or RAD51D Mdoule 2:... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003357-29 | Sponsor Protocol Number: PROICM2019-08INT | Start Date*: 2019-12-03 |
Sponsor Name:Institut Régional du Cancer de Montpellier (ICM) | ||
Full Title: Intensive intraperitoneal therapy in advanced ovarian cancer combining cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (HIPEC) and postoperative intraperitoneal chemotherapy (I... | ||
Medical condition: Patient with high-grade serous (high grade according to MD Anderson, grade II and III according to Silverman) ovarian or tubal or primitive peritoneal histologically proven cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002326-24 | Sponsor Protocol Number: ALKS4230-007 | Start Date*: 2023-02-13 | |||||||||||||||||||||
Sponsor Name:Mural Oncology, Inc. | |||||||||||||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label, Randomized Study of Nemvaleukin Alfa in Combination With Pembrolizumab Versus Investigator’s Choice Chemotherapy in Patients With Platinum-Resistant Epithelial O... | |||||||||||||||||||||||
Medical condition: Patients with Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PL (Prematurely Ended) IT (Trial now transitioned) NO (Trial now transitioned) AT (Trial now transitioned) LT (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001005-82 | Sponsor Protocol Number: TALL/IP/2 | Start Date*: 2015-05-05 |
Sponsor Name:Galileo Research Srl | ||
Full Title: Phase II trial of intraperitoneal MHC unrestricted adoptive cell therapy with TALL-104 cells in patients with ovarian carcinoma with minimal or microscopic residual disease at second look laparotom... | ||
Medical condition: Ovarian carcinoma (FIGO stage IIIA and IIIB/IIIC/IV; patients with extra-abdominal disease will be excluded by the study unless those with pleural effusion) with minimal/microscopic residual disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003412-31 | Sponsor Protocol Number: BROVALE-2012(BC-POF2012) | Start Date*: 2012-10-01 | |||||||||||||||||||||
Sponsor Name:CUB - Hôpital Erasme | |||||||||||||||||||||||
Full Title: Efficiency and Safety of Ovarian Stimulation with Letrozole for fertility preservation in breast cancer patients. | |||||||||||||||||||||||
Medical condition: The aim of this trial is to offer a safe and efficient alternative protocol to preserve fertility by storing oocytes in breast cancer patients before chemotherapy. Letrozole, an inhibitor of aromat... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001346-41 | Sponsor Protocol Number: ICON6 | Start Date*: 2007-07-16 | |||||||||||||||||||||
Sponsor Name:Medical Research Council | |||||||||||||||||||||||
Full Title: A double-blind, placebo-controlled, three arm randomised multi-centre Gynaecologic Cancer InterGroup trial of AZD2171, in combination with platinum-based chemotherapy and as a single agent maintena... | |||||||||||||||||||||||
Medical condition: epitehlial ovarian carcinoma, fallopian tube carcinoma, primary serous peritoneal carcinoma relapsing more than 6 months after completion of first-line platinum based chemotherapy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000517-20 | Sponsor Protocol Number: CO-338-017 | Start Date*: 2013-11-26 | |||||||||||||||||||||
Sponsor Name:Clovis Oncology, Inc. | |||||||||||||||||||||||
Full Title: A Phase 2, Open-Label Study of Rucaparib in Patients with Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
Medical condition: Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003287-39 | Sponsor Protocol Number: PRO-105 | Start Date*: 2017-07-05 |
Sponsor Name:NuCana plc | ||
Full Title: A Phase II Open-Label Study of NUC-1031 in Patients with Platinum-Resistant Ovarian Cancer | ||
Medical condition: Platinum-resistant epithelial cancer of the ovary, fallopian tube or primary peritoneum (here termed ‘ovarian cancer’), who have been treated with 3 or more prior chemotherapy regimens. | ||
Disease: | ||
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: 2007-001432-31 | Sponsor Protocol Number: CA190001 | Start Date*: 2008-04-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 1/2a, Ascending Multiple-Dose Study to Evaluate the Safety, Efficacy and Pharmacokinetics of BMS-753493 in Subjects with Advanced Cancer. Revised Protocol 02, incorporating Protocol Amend... | |||||||||||||
Medical condition: Advanced Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003014-18 | Sponsor Protocol Number: TEO-NEF-01 | Start Date*: 2012-03-05 | ||||||||||||||||||||||||||
Sponsor Name:Vicente Barrio Lucia | ||||||||||||||||||||||||||||
Full Title: Double blind randomized controlled clinical trial to evaluate the efficacy and safety of theophyline in the prevention of nephrotoxicity associated with cisplatin in oncology | ||||||||||||||||||||||||||||
Medical condition: Eficacia del tratamiento con teofilina para evitar el descenso del 25 %, estimado en el grupo placebo del filtrado glomerular medido con EDTA-Cr51 en pacientes oncológicos bajo tratamiento quimiote... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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