- Trials with a EudraCT protocol (492)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
492 result(s) found for: Ovarian pregnancy.
Displaying page 1 of 25.
| EudraCT Number: 2006-004484-54 | Sponsor Protocol Number: IP-CAT-OC-02 | Start Date*: 2007-08-30 | ||||||||||||||||||||||||||
| Sponsor Name:Fresenius Biotech GmbH | ||||||||||||||||||||||||||||
| Full Title: Multicenter, single-arm, phase II study of the tri functional antibody catumaxomab (anti EpCAM x anti-CD3) administered intra- and postoperatively in patients with epithelial ovarian cancer | ||||||||||||||||||||||||||||
| Medical condition: Epithelial Ovarian Cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-004400-19 | Sponsor Protocol Number: 1707-FIVI-084-MV | Start Date*: 2019-05-30 | |||||||||||
| Sponsor Name:IVIRMA MADRID | |||||||||||||
| Full Title: Study of the effects of telomerase reactivation with Danazol on ovarian function. A Pilot Study. | |||||||||||||
| Medical condition: low ovarian reserve | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001616-30 | Sponsor Protocol Number: 000071 | Start Date*: 2013-09-17 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: A controlled, assessor-blind, parallel groups, multicentre, multinational trial evaluating the immunogenicity of FE 999049 in repeated cycles of controlled ovarian stimulation in women undergoing a... | |||||||||||||
| Medical condition: Infertility | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) DK (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003817-16 | Sponsor Protocol Number: EMR200061-005 | Start Date*: 2014-02-05 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: A phase III, randomized, controlled, single-blind, multicentre, parallel arm trial to assess the efficacy and safety of Pergoveris® (follitropin alfa and lutropin alfa) and GONAL-f® (follitropin... | |||||||||||||
| Medical condition: Poor Ovarian Response i.e. a failure to respond adequately to standard ART (assisted reproductive technologies) protocols and to recruit adequate follicles | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) EE (Completed) HU (Completed) BE (Completed) GB (Completed) NL (Completed) DK (Completed) LV (Completed) ES (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004429-41 | Sponsor Protocol Number: BAY43-9006/12007 | Start Date*: 2008-10-03 | |||||||||||||||||||||
| Sponsor Name:Bayer Healthcare AG | |||||||||||||||||||||||
| Full Title: A Double-Blind, Randomized Phase II Study Evaluating the Efficacy and Safety of Sorafenib Compared to Placebo in Ovarian Epithelial Cancer or Primary Peritoneal Cancer Patients who have achieved a ... | |||||||||||||||||||||||
| Medical condition: The study population will include patients with FIGO stage III or IV ovarian cancer or primary peritoneal cancer who have had extensive debulkment surgery and who have achieved a clinical complete ... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) NL (Completed) IT (Completed) ES (Completed) FR (Completed) FI (Completed) DE (Completed) PL (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-006220-40 | Sponsor Protocol Number: 2022-0101-01 | Start Date*: 2022-06-30 | ||||||||||||||||||||||||||
| Sponsor Name:Hvidovre Hospital, Department of Gynecology | ||||||||||||||||||||||||||||
| Full Title: Double-blinded randomized placebo-controlled trial on tacrolimus in women with an euploid pregnancy loss and PCOS and/or thyroid autoimmunity | ||||||||||||||||||||||||||||
| Medical condition: Polycystic ovarian syndrome and/or thyroid autoimmunity in combination with an euploid pregnancy loss | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2009-012666-31 | Sponsor Protocol Number: OG09/8956 | Start Date*: 2009-11-11 | |||||||||||
| Sponsor Name:Leeds Teaching Hospitals and University of Leeds | |||||||||||||
| Full Title: The role of progesterone support and genetic polymorphisms for inflammatory cytokines on the risk of developing ovarian hyperstimulation syndrome (OHSS) in women undergoing In-Vitro fertilisation/I... | |||||||||||||
| Medical condition: Ovarian Hyperstimulation syndrome | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001457-28 | Sponsor Protocol Number: CAM203 | Start Date*: 2004-09-09 | |||||||||||
| Sponsor Name:CELL THERAPEUTICS EUROPE | |||||||||||||
| Full Title: Phase II open label study of CT-2106 as a single agent in patients with advanced metastatic ovarian cancer who have failed one prior platinum and taxane based regimen | |||||||||||||
| Medical condition: Treatment of patients with advanced ovarian cancer who have failed one prior platinum and taxane based regimen | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-011041-12 | Sponsor Protocol Number: ET-A-018-09 | Start Date*: 2009-07-23 | |||||||||||
| Sponsor Name:Pharma Mar S.A. | |||||||||||||
| Full Title: Étude multicentrique de phase Ib-II en escalade de dose de la trabectédine (Yondelis®) en association avec l’oxaliplatine chez des patientes atteintes d’un cancer de l’ovaire avancé prétraité. | |||||||||||||
| Medical condition: Pretreated Advanced Ovarian Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001323-38 | Sponsor Protocol Number: SOV02 | Start Date*: 2013-08-30 | |||||||||||
| Sponsor Name:SOTIO a.s. | |||||||||||||
| Full Title: A randomized, open-label, parallel group, multi-center Phase II clinical trial evaluating effect of addition of DCVAC/OvCa to standard chemotherapy (carboplatin and gemcitabine) in women with rel... | |||||||||||||
| Medical condition: epithelial ovarian carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007925-38 | Sponsor Protocol Number: HE 4/09 | Start Date*: 2009-04-07 | |||||||||||
| Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||
| Full Title: STUDY OF THE mTOR INHIBITOR TEMSIROLIMUS (CCI-779) IN PATIENTS WITH CA125 ONLY RELAPSE OF OVARIAN CANCER A phase II study by the Hellenic Cooperative Oncology Group | |||||||||||||
| Medical condition: Ovarian cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001325-24 | Sponsor Protocol Number: SOV03 | Start Date*: 2013-08-30 | |||||||||||
| Sponsor Name:SOTIO a.s. | |||||||||||||
| Full Title: A randomized, open-label, parallel group, multi-center Phase II clinical trial evaluating effect of addition of DCVAC/OvCa to standard chemotherapy in women with relapsed platinum resistant epith... | |||||||||||||
| Medical condition: epithelial ovarian carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001755-45 | Sponsor Protocol Number: OX4325 | Start Date*: 2016-09-12 | |||||||||||||||||||||
| Sponsor Name:Mateon Therapeutics, Inc. | |||||||||||||||||||||||
| Full Title: FOCUS: A Multicenter, Multinational, Double-blind, 2-Arm, Randomized, Phase 2/3, Study of Physician’s Choice Chemotherapy (PCC) (Weekly Paclitaxel or Pegylated Liposomal Doxorubicin [PLD]) Plus Bev... | |||||||||||||||||||||||
| Medical condition: Platinum-resistant, recurrent, epithelial ovarian, primary peritoneal or fallopian tube cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-004850-14 | Sponsor Protocol Number: GEICO-1601 | Start Date*: 2017-11-13 | |||||||||||||||||||||
| Sponsor Name:Grupo Español de Investigación en Cancer de Ovario | |||||||||||||||||||||||
| Full Title: Multicentric Single Arm Phase II Clinical Trial, to Evaluate Safety and Efficacy of the Combination of Olaparib and PLD for Platinum Resistant Ovarian Primary Peritoneal Carcinoma, and Fallopian Tu... | |||||||||||||||||||||||
| Medical condition: Platinum resistant ovarian primary peritoneal carcinoma, and fallopian tube cancer patients. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-004364-25 | Sponsor Protocol Number: GINECO-OV244b | Start Date*: 2021-01-08 | ||||||||||||||||
| Sponsor Name:ARCAGY-GINECO | ||||||||||||||||||
| Full Title: Randomized Phase II study comparing neo-epitope based vaccine OSE2101 (TEDOPI®) with or without anti-PD1 (Pembrolizumab) versus best supportive care as maintenance treatment in platinum-sensitive r... | ||||||||||||||||||
| Medical condition: 1st or 2nd platinum-sensitive recurrent ovarian cancer with controlled disease after platinum based chemotherapy. | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-000247-32 | Sponsor Protocol Number: MAXINOVO | Start Date*: 2020-11-03 |
| Sponsor Name:REPRODUCCION BILBAO (GINEGORAMA SL) | ||
| Full Title: ACTIVATION OF PRIMORDIAL FOLLICULES AMONG WOMEN WITH POOR OVARIAN RESERVE BY USIN GROWTH FACTORS. | ||
| Medical condition: The reproductive capacity of women depends on two factors: the number of follicles in the ovaries and the quality of oocytes within those follicles. Premature ovarian failure (POF) and poor ovaria... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002571-25 | Sponsor Protocol Number: 2017.corifollitropinalfa_IVM | Start Date*: 2017-10-18 | |||||||||||
| Sponsor Name:UZ Brussel | |||||||||||||
| Full Title: A comparison between corifollitropin alfa and recombinant FSH for follicular recruitment in women with polycystic ovaries who undergo IVM treatment | |||||||||||||
| Medical condition: Infertile patients with polycystic ovaries | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005197-40 | Sponsor Protocol Number: I1D-MC-JIAE | Start Date*: 2012-07-20 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 1b/2 Study of LY2228820, a p38MAPK Inhibitor, plus Gemcitabine and Carboplatin versus Gemcitabine and Carboplatin for Women with Platinum-Sensit... | |||||||||||||
| Medical condition: Epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005221-12 | Sponsor Protocol Number: OCTOPUS-2014 | Start Date*: 2015-09-07 | |||||||||||||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||||||||||||
| Full Title: OCTOPUS: Ovarian Cancer Trials of Weekly Paclitaxel - Umbrella Study A Randomised, Phase II Umbrella Trial of a Weekly Paclitxel +/- Novel Agents in Platinum-Resistant Ovarian Cancer | |||||||||||||||||||||||
| Medical condition: Ovarian Cancer | |||||||||||||||||||||||
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| Population Age: | Gender: Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2018-003484-56 | Sponsor Protocol Number: BOLDOS-18 | Start Date*: 2019-12-26 | |||||||||||
| Sponsor Name:Miguel Caballero Campo | |||||||||||||
| Full Title: Efficacy of corifolitropin alfa in double ovarian stimulation compared with two conventional ovarian stimulation cycles for embryo accmulation in low responder patients. Multicenter randomized cont... | |||||||||||||
| Medical condition: Infertility in patients requiring in vitro fertilization treatment with poor ovarian response profile, defined by Bologna Criteria. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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