- Trials with a EudraCT protocol (330)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
330 result(s) found for: Endometrial.
Displaying page 17 of 17.
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: 2019-004046-16 | Sponsor Protocol Number: IMC-F106C-101 | Start Date*: 2020-04-08 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Immunocore Ltd. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2 First-in-Human Study of the Safety and Efficacy of IMC-F106C as a Single Agent and in Combination with Checkpoint Inhibitors in HLA-A*02:01-Positive Participants with Advanced PRAME-Pos... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: HLA-A*02:01-Positive Participants with Advanced PRAME-Positive Cancers. Study IMC-F106C-101 will enroll participants with advanced cancers, including unresectable or metastatic melanoma, ovarian ca... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004372-22 | Sponsor Protocol Number: Ti-061-101 | Start Date*: 2017-04-05 | ||||||||||||||||
Sponsor Name:Tioma Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 1-2 Study of Ti-061 Alone and in combination with other anti-cancer agents in Patients with Advanced Malignancies | ||||||||||||||||||
Medical condition: Advanced malignancies | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000630-37 | Sponsor Protocol Number: 308601 | Start Date*: 2004-11-29 |
Sponsor Name:Schering AG | ||
Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the safety, tolerability and efficacy of the CCR1 antagonist ZK 811752, given orally in a dose of 600 m... | ||
Medical condition: Endometrial pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) SE (Completed) ES (Completed) CZ (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003802-30 | Sponsor Protocol Number: OMO-103-01 | Start Date*: 2022-09-21 | ||||||||||||||||||||||||||
Sponsor Name:Peptomyc S.L. | ||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study to evaluate the Safety, Pharmacokinetics, and Anti-Tumour Activity of the Myc Inhibitor OMO-103 administered intravenously in Patients with Advanced Tumours. | ||||||||||||||||||||||||||||
Medical condition: Solid tumours | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2013-000762-11 | Sponsor Protocol Number: 62113-55115 | Start Date*: 2014-10-20 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: A randomized double-blind phase II study evaluating the role of maintenance therapy with cabozantinib in High Grade Undifferentiated Uterine Sarcoma (HGUS) after stabilization or response to doxoru... | |||||||||||||
Medical condition: High Grade Undifferentiated Uterine Sarcoma (HGUS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) ES (Completed) DE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002872-42 | Sponsor Protocol Number: PUMA-NER-5201 | Start Date*: 2014-03-25 | |||||||||||
Sponsor Name:Puma Biotechnology, Inc | |||||||||||||
Full Title: An Open-Label, Phase 2 Study of Neratinib in Patients With Solid Tumors With Somatic Human Epidermal Growth Factor Receptor (EGFR, HER2, HER3) Mutations or EGFR gene amplification | |||||||||||||
Medical condition: Cancer tumor with somatic human epidermal growth factor receptor mutation (EGFR, ERBB2 (HER2), ERBB3 (HER3) or EGFR gene amplification | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) FI (Completed) GB (GB - no longer in EU/EEA) DK (Completed) BE (Completed) FR (Ongoing) IE (Completed) | |||||||||||||
Trial results: View results |
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: 2010-024394-39 | Sponsor Protocol Number: CBEZ235B2201 | Start Date*: 2011-05-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase II study of orally administered BEZ235 monotherapy in patients with hormone receptor positive, HER2 negative, metastatic breast cancer, with or without PI3K activated pathway | |||||||||||||
Medical condition: Patients who have experienced progression of disease after first-line antineoplasic treatment of advanced endometrial carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
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