- Trials with a EudraCT protocol (159)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
159 result(s) found for: CA-125.
Displaying page 2 of 8.
EudraCT Number: 2013-001276-38 | Sponsor Protocol Number: ColoAd1-2001 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:PsiOxus Therapeutics Ltd | |||||||||||||
Full Title: A Clinical Study Of ColoAd1 Administered Intraperitoneally: Dose Finding and Proof of Concept in Platinum-Resistant Epithelial Ovarian Cancer | |||||||||||||
Medical condition: Epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004472-30 | Sponsor Protocol Number: MITO23 | Start Date*: 2015-12-02 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Randomized phase III trial on Trabectedin (ET-743) vs clinician’s choice chemotherapy in recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
Medical condition: recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008336-85 | Sponsor Protocol Number: MO22225 | Start Date*: 2009-06-05 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||||||||||||
Full Title: A single-arm Phase II clinical study of the combination of carboplatin and weekly paclitaxel plus bevacizumab as first-line treatment in patients with epithelial ovarian cancer | |||||||||||||||||||||||
Medical condition: Epithelial ovarian cancer, fallopian tube or primary peritoneal carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) NL (Completed) GB (Completed) SE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000265-67 | Sponsor Protocol Number: APR-486 | Start Date*: 2017-08-01 | |||||||||||
Sponsor Name:Aprea Therapeutics AB | |||||||||||||
Full Title: PiSARRO-R: p53 Suppressor Activation in Platinum-Resistant High Grade Serous Ovarian Cancer, a Phase II Study of Systemic Pegylated Liposomal Doxorubicin Chemotherapy With APR-246 | |||||||||||||
Medical condition: Platinum-resistant high grade serous ovarian carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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: 2010-018849-59 | Sponsor Protocol Number: GMIHO-008/2009_AG56 | Start Date*: 2011-05-10 | |||||||||||
Sponsor Name:GMIHO Gesellschaft für Medizinische Innovation - Hämatologie und Onkologie mbH | |||||||||||||
Full Title: A randomized phase II trial of standard carboplatin-based chemotherapy with or without panitumumab in platinum-sensitive recurrent ovarian cancer | |||||||||||||
Medical condition: Platinum-sensitive recurrent ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000400-42 | Sponsor Protocol Number: ZP-PDProtec-201 | Start Date*: 2014-05-13 |
Sponsor Name:Zytoprotec GmbH | ||
Full Title: Prospective, randomized, multi-center, double-blind, controlled, two-period, two-treatment, crossover, phase II trial to evaluate the safety and efficacy of PD-protec® in peritoneal dialysis in pat... | ||
Medical condition: End Stage Renal Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005576-26 | Sponsor Protocol Number: 08-PIR-04 | Start Date*: 2009-02-19 | |||||||||||
Sponsor Name:Nektar Therapeutics | |||||||||||||
Full Title: A Multicenter, Open-Label, Phase 2 Study to Evaluate the Safety and Efficacy of NKTR-102 (PEG-Irinotecan) When Given on a Q14 Day or a Q21 Day Schedule in Patients with Metastatic or Unresectable L... | |||||||||||||
Medical condition: Metastatic or Unresectable Locally Advanced Platinum-Resistant Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003209-10 | Sponsor Protocol Number: ML18583 | Start Date*: 2005-10-18 |
Sponsor Name:Tampere University Hospital | ||
Full Title: VEGF, VEGFR1 and VEGFR2 expression in serous epithelial ovarian carcinoma, and its association to the efficacy of bevacizumab combined with paclitaxel and carboplatin as first line treatment | ||
Medical condition: FIGO Stage III-IV serous epithelial ovarian carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000886-30 | Sponsor Protocol Number: D6010C00004 | Start Date*: 2015-07-29 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Multicentre Phase II Study of AZD1775 plus Chemotherapy in Patients with Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer. | ||
Medical condition: Platinum-Resistant Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001211-75 | Sponsor Protocol Number: D0816C00002 | Start Date*: 2013-11-15 | ||||||||||||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||||||||||||
Full Title: A Phase III Randomised, Double Blind, Placebo Controlled, Multicentre Study of Olaparib Maintenance Monotherapy in Platinum Sensitive Relapsed BRCA Mutated Ovarian Cancer Patients who are in Comple... | ||||||||||||||||||||||||||||
Medical condition: BRCA Mutated Platinum Sensitive Relapse (PSR) high grade Serous Ovarian Cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) IT (Completed) ES (Ongoing) FR (Ongoing) PL (Completed) DE (Completed) BE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000825-18 | Sponsor Protocol Number: CSET2020/3047 | Start Date*: 2020-05-12 | |||||||||||
Sponsor Name:Gustave Roussy | |||||||||||||
Full Title: An open-label, multicentric, phase Ib/II study to assess the safety and efficacy of AsiDNATM, a DNA repair inhibitor, administered intravenously in addition to Niraparib in patients with relapsed p... | |||||||||||||
Medical condition: Relapsed platinum sensitive ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020233-56 | Sponsor Protocol Number: DC-006 | Start Date*: 2011-03-24 |
Sponsor Name:Oslo University Hospital | ||
Full Title: PHASE I/II TRIAL OF VACCINE THERAPY IN RELAPSED AND PLATINUM RESISTANT EPITHELIAL OVARIAN CANCER PATIENTS USING AUTOLOGOUS DENDRITIC CELLS LOADED WITH AMPLIFIED OVARIAN CANCER STEM CELL mRNA, hTE... | ||
Medical condition: Relapsed and platinum resistant epithelial ovarian carcinoma patients that have received one line of non-platinum chemotherapy in resistance disease setting. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005181-20 | Sponsor Protocol Number: CEPO906A2303 | Start Date*: 2006-05-19 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, parallel group, open-label, active controlled, multicenter Phase III trial of Patupilone (EPO906) versus pegylated liposomal doxorubicin (Doxil/Caelyx) in taxane/platinum refractory/r... | ||
Medical condition: Approximately 75% of women with ovarian cancer present advanced disease. Survival is highly dependent on the stage of disease at the initiation of treatment. Favorable prognostic factors include yo... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) ES (Completed) FI (Completed) DK (Completed) HU (Completed) GR (Completed) IT (Completed) IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001836-44 | Sponsor Protocol Number: UCL/11/0119 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A Phase II Trial to Assess the Activity of TroVax® (MVA-5T4) Versus Placebo in Patients with Relapsed Asymptomatic Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer. | |||||||||||||
Medical condition: Patients with relapsed asymptomatic epithelial ovarian, fallopian tube or primary peritoneal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000952-11 | Sponsor Protocol Number: PR-30-5017-C | Start Date*: 2016-07-01 | |||||||||||
Sponsor Name:TESARO, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of Niraparib Maintenance Treatment in Patients with Advanced Ovarian Cancer Following Response on Front-Line Platinum-Base... | |||||||||||||
Medical condition: Homologous recombination deficiency advanced ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) SE (Trial now transitioned) IE (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) GB (GB - no longer in EU/EEA) HU (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
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: 2009-011922-33 | Sponsor Protocol Number: TRIAS2009 | Start Date*: 2009-11-24 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: A randomized, double-blind, placebo controlled, multicenter Phase II study to assess the efficacy and safety of Sorafenib added to standard treatment with Topotecan in patients with platinum-resist... | ||
Medical condition: This study is a prospective, randomized, double-blind, multi-center placebo-controlled phase II study in order to determine progression-free survival of patients with platinum-resistant or refract... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005050-35 | Sponsor Protocol Number: 30102012 | Start Date*: 2014-12-01 | ||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
Full Title: Phase Ib/II study of metformin in combination with carboplatin/paclitaxel chemotherapy in patients with advanced ovarian cancer | ||||||||||||||||||
Medical condition: advanced ovarian cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005872-29 | Sponsor Protocol Number: MORAb-003-004 | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Phase 3 Study to Assess the Efficacy and Safety of Weekly Farletuzumab (MORAb-003) in Combination with Carboplatin and Taxane in Subjects with Plati... | |||||||||||||
Medical condition: First relapse of platinum-sensitive non-mucinous epithelial ovarian cancer including primary peritoneal or fallopian tube malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) PT (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) FR (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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