- Trials with a EudraCT protocol (330)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
330 result(s) found for: Endometrial.
Displaying page 3 of 17.
EudraCT Number: 2010-022015-19 | Sponsor Protocol Number: CBKM120C2201 | Start Date*: 2011-04-26 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A | |||||||||||||
Full Title: Estudio de fase II, de una sola rama, de BKM120 administrado por vía oral como tratamiento de segunda línea en pacientes con carcinoma endometrial avanzado | |||||||||||||
Medical condition: Mujeres adultas con carcinoma endometrial avanzado cuya enfermedad ha progresado durante o después del tratamiento antineoplásico de primera línea para la enfermedad avanzada. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) BE (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002663-26 | Sponsor Protocol Number: AEZS-108-040 | Start Date*: 2007-12-05 | |||||||||||||||||||||||||||||||
Sponsor Name:AEterna Zentaris GmbH | |||||||||||||||||||||||||||||||||
Full Title: Antitumoral activity and safety of AEZS-108 (AN-152), a LHRH agonist linked doxorubicin, in women with LHRH receptor positive gynecological tumors | |||||||||||||||||||||||||||||||||
Medical condition: Histologically confirmed malignancy of ovary or endometrium that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective and LHR... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) BG (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001624-17 | Sponsor Protocol Number: 210321 | Start Date*: 2021-07-21 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Safety of oral micronized progesterone versus norethisterone acetate in continuous combination with oral estrogen as menopausal hormone therapy – a double-blind randomized study- PROBES study (Prog... | ||
Medical condition: Climacteric symptoms | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004364-11 | Sponsor Protocol Number: 69HCL15_0321 | Start Date*: 2016-03-07 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: ENDOLA A PHASE I/II TRIAL TO ASSESS THE SAFETY AND EFFICACY OF METRONOMIC CYCLOPHOSPHAMIDE, METFORMIN AND OLAPARIB IN RECURRENT ADVANCED/METASTATIC ENDOMETRIAL CANCER PATIENTS | |||||||||||||
Medical condition: - Patients with histologically and/or cytologically documented endometrial carcinoma (type I or type II), recurrent after platinum-based chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023081-52 | Sponsor Protocol Number: ENGOT-EN2-DGCG | Start Date*: 2011-01-25 | ||||||||||||||||
Sponsor Name:Danish Gynaecological Cancer Group (DGCG) | ||||||||||||||||||
Full Title: A phase II Trial of postoperative chemotherapy or no further treatment for patients with node-negative stage I-II intermediate or high risk endometrial cancer. | ||||||||||||||||||
Medical condition: Endometrial cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) SE (Completed) BE (Completed) FI (Completed) AT (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) DE (Completed) IT (Completed) NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001815-30 | Sponsor Protocol Number: SGUL/SGH 001 | Start Date*: 2006-06-05 | |||||||||||
Sponsor Name:St George's, University of London (SGUL) [...] | |||||||||||||
Full Title: Prevention Of Endometrial Tumours (POET) | |||||||||||||
Medical condition: Endometrial cancer/tumours in women with Hereditary Non-polyposis Colorectal Cancer (HNPCC) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006841-25 | Sponsor Protocol Number: CRAD001CCH08t | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Oncology Institute of Southern Switzerland | |||||||||||||
Full Title: Phase II study of the combination of RAD001 and Letrozole in patients with recurrent endometrial cancer | |||||||||||||
Medical condition: Recurrent endometrial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002606-18 | Sponsor Protocol Number: D1600C00001 | Start Date*: 2008-07-10 | ||||||||||||||||
Sponsor Name:Astrazeneca AB | ||||||||||||||||||
Full Title: A Phase I/II, Open Label, Multi-centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of the Tor Kinase Inhibitor AZD8055 Administered Orally to Patients with A... | ||||||||||||||||||
Medical condition: Advanced solid tumours and lymphomas | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001103-35 | Sponsor Protocol Number: NSGO -EC - 0302 | Start Date*: 2004-08-20 |
Sponsor Name:Nordic Society for Gynecologic Oncology | ||
Full Title: Exemestane in Advanced or Recurrent Endometrial Carcinoma. A multicentre non-randomized Phase II study | ||
Medical condition: Advanced or recurrent endometrial carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005394-37 | Sponsor Protocol Number: C31004 | Start Date*: 2016-08-31 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized Study of MLN0128 (a Dual TORC1/2 Inhibitor), MLN0128+MLN1117 (a PI3Kα Inhibitor), Weekly Paclitaxel, or the Combination of Weekly Paclitaxel and MLN0128 in Women With Advanced... | |||||||||||||
Medical condition: Advanced, Recurrent, or Persistent Endometrial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003424-17 | Sponsor Protocol Number: MK3475-B21/ENGOT-en11/GOG-3053 | Start Date*: 2021-01-11 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Study of Pembrolizumab versus Placebo in Combination With Adjuvant Chemotherapy With or Without Radiotherapy for the Treatment of Newly Diagnosed High-Risk Endom... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) AT (Trial now transitioned) PL (Trial now transitioned) NO (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001737-40 | Sponsor Protocol Number: S55201 | Start Date*: 2013-08-12 |
Sponsor Name:UZ Leuven | ||
Full Title: Effect of curcumin addition to standard treatment on tumour-induced inflammation in endometrial carcinoma | ||
Medical condition: endometrial carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004535-24 | Sponsor Protocol Number: RLY-4008-101 | Start Date*: 2021-07-07 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Relay Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A First-in-Human Study of Highly Selective FGFR2 inhibitor, RLY-4008, in Patients with Intrahepatic Cholangiocarcinoma (ICC) and other Advanced Solid Tumors | ||||||||||||||||||||||||||||||||||||||
Medical condition: Unresectable or metastatic cholangiocarcinoma (CCA), other advanced solid tumors with an FGFR2-alteration or other potential FGFR2-dependent tumors | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) NL (Trial now transitioned) DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2017-002904-29 | Sponsor Protocol Number: INCB01158-203 | Start Date*: 2017-12-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, and Efficacy of INCB001158 in Combination With Chemotherapy, in Subjects With Advanced or Metastatic Solid Tumors. | |||||||||||||||||||||||||||||||||
Medical condition: Phase 1: Advanced or metastatic solid tumors Phase 2: Advanced/metastatic microsatellite stable colorectal cancer (MSS-CRC), biliary tract cancer (BTC), gastroesophageal cancer (GC), and endometri... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003600-12 | Sponsor Protocol Number: MORAb-202-G000-201 | Start Date*: 2022-07-25 | ||||||||||||||||||||||||||
Sponsor Name:Eisai Limited | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-Label Phase 1/2 Trial Evaluating the Safety, Tolerability, and Efficacy of MORAb-202, a folate receptor alpha (FRα)-targeting antibody-drug conjugate (ADC) in Subjects With Sele... | ||||||||||||||||||||||||||||
Medical condition: Solid tumors expressing folate receptor alpha in 4 tumor types: platinum resistant ovarian cancer, triple-negative breast cancer (TNBC), endometrial cancer (EC), and non-small cell lung cancer aden... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003062-32 | Sponsor Protocol Number: B1271004 | Start Date*: 2011-12-20 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A RANDOMIZED PHASE 2 NON-COMPARATIVE STUDY OF THE EFFICACY OF PF-04691502 AND PF-05212384 IN PATIENTS WITH RECURRENT ENDOMETRIAL CANCER | |||||||||||||
Medical condition: RECURRENT ENDOMETRIAL CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) ES (Completed) PL (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004638-99 | Sponsor Protocol Number: 2105xx1 | Start Date*: 2017-11-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine and PET | |||||||||||||||||||||||||||||||||
Full Title: Phase II trial: uPAR PET/CT and FDG PET/CT for preoperative staging of gynecological cancers | |||||||||||||||||||||||||||||||||
Medical condition: gynecological cancers: Vulvar cancer endometrial cancer (uterine cancer) cervical cancer ovarian cancer | |||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005481-18 | Sponsor Protocol Number: BNT142-01 | Start Date*: 2022-04-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:BioNTech SE | ||||||||||||||||||||||||||||||||||||||
Full Title: First-in-human, open-label, multicenter, Phase I/IIa, dose escalation trial with expansion cohorts to evaluate safety and preliminary efficacy of BNT142 in patients with CLDN6-positive advanced sol... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Claudin 6 (CLDN6)-positive advanced solid tumors | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002918-19 | Sponsor Protocol Number: VEG110190 | Start Date*: 2007-09-06 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithkline Research & Development Limited | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase II, Open-Label, Multicenter Feasibility Study of Pazopanib, Carboplatin, and Paclitaxel in Women with Previously Untreated, Advanced Gynaecological Tumors | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: previously untreated, advanced gynaecological tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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