- Trials with a EudraCT protocol (3,231)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
3,231 result(s) found for: Cancer screening.
Displaying page 1 of 162.
EudraCT Number: 2020-002210-41 | Sponsor Protocol Number: 29BRC20.0021 | Start Date*: 2020-06-29 | ||||||||||||||||
Sponsor Name:CHRU de Brest | ||||||||||||||||||
Full Title: Screening for occult malignancy using 18F-Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (FDG PET/CT) in patients with unprovoked venous thromboembolism | ||||||||||||||||||
Medical condition: Embolism venous Neoplasm malignant | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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: 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: 2021-004277-31 | Sponsor Protocol Number: E012-HPV | Start Date*: 2021-12-23 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:eTheRNA immunotherapies NV | ||||||||||||||||||||||||||||||||||||||
Full Title: A phase I/IIa open label study to assess the safety, tolerability, immunogenicity and clinical activity of EI-201 mRNA immunotherapy given intravenously in subjects with recurrent or metastatic HPV... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Incurable recurrent or metastatic (R/M) HPV16-positive (HPV16+) tumors (e.g. oropharyngeal cancer, cervical, vulvar, vaginal, anal, penile cancer, etc.) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) NL (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021900-93 | Sponsor Protocol Number: CLIN1001 PCM301 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:STEBA BIOTECH SA | |||||||||||||
Full Title: A European randomised Phase 3 study to assess the efficacy and safety of TOOKAD® Soluble for low risk localised prostate cancer compared to Active Surveillance | |||||||||||||
Medical condition: Low-risk prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) DE (Completed) NL (Completed) BE (Completed) SE (Completed) FI (Completed) DK (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005245-37 | Sponsor Protocol Number: M06-880 | Start Date*: 2008-04-17 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: An Open-Label, Randomized, Phase 2 Study of Efficacy and Tolerability of ABT-869 in Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) SE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001192-39 | Sponsor Protocol Number: P11-1 | Start Date*: 2012-01-26 | |||||||||||||||||||||||||||||||
Sponsor Name:Dendreon Corporation | |||||||||||||||||||||||||||||||||
Full Title: AN OPEN-LABEL STUDY OF SIPULEUCEL-T IN EUROPEAN MEN WITH METASTATIC, CASTRATE RESISTANT PROSTATE CANCER | |||||||||||||||||||||||||||||||||
Medical condition: metastatic castrate resistant prostate cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) GB (Completed) NL (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003642-26 | Sponsor Protocol Number: 3116001 | Start Date*: 2014-12-17 | ||||||||||||||||
Sponsor Name:Orion Corporation Orion Pharma | ||||||||||||||||||
Full Title: SAFETY AND PHARMACOKINETICS OF ODM-204 IN PATIENTS WITH METASTATIC CASTRATION-RESISTANT PROSTATE CANCER (CRPC): OPEN, NONRANDOMISED, UNCONTROLLED, MULTICENTRE, DOSE ESCALATION, FIRST-IN-MAN STUDY W... | ||||||||||||||||||
Medical condition: Metastatic castration resistant prostate cancer (mCRPC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: FI (Completed) GB (Completed) LV (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000299-33 | Sponsor Protocol Number: AGO-GYN8 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:AGO Research GmbH | ||||||||||||||||||
Full Title: Efficacy, tolerability and safety of Temsirolimus in women with platinum-refractory ovarian carcinoma or advanced endometrial carcinoma | ||||||||||||||||||
Medical condition: platinum-refractory ovarian carcinoma or advanced endometrial carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004405-30 | Sponsor Protocol Number: ARN-AR18-CT-102 | Start Date*: 2014-02-12 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Arno Therapeutics Inc | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1 Study of Onapristone in Patients with Advanced Castration-resistant Prostate Cancer | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced Castration-resistant Prostate Cancer | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003715-38 | Sponsor Protocol Number: D4190C00006 | Start Date*: 2016-05-12 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:MedImmune LLC | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1b Open-label Study to Evaluate the Safety and Tolerability of MEDI4736 in Combination with Tremelimumab in Subjects with Advanced Non-small Cell Lung Cancer | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Locally advanced or metastatic squamous or nonsquamous non- small cell lung cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) ES (Completed) DE (Completed) GB (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002161-30 | Sponsor Protocol Number: 1302.5 | Start Date*: 2015-09-07 | |||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind Phase III trial to evaluate efficacy and safety of BI 695502 plus chemotherapy versus Avastin® plus chemotherapy in patients with advanced nonsquamous Non-Sm... | |||||||||||||||||||||||
Medical condition: Recurrent or metastatic disease (Stage IV), histologically or cytologically confirmed advanced nonsquamous Non-Small Cell Lung Cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) PT (Completed) ES (Completed) DE (Completed) PL (Completed) HR (Completed) GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001436-10 | Sponsor Protocol Number: INCB18424-266 | Start Date*: 2015-02-26 | |||||||||||||||||||||||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind Phase 2 Study of Ruxolitinib or Placebo in Combination With Pemetrexed/Cisplatin and Pemetrexed Maintenance for Initial Treatment of Subjects With Nonsquamous Non–Small C... | |||||||||||||||||||||||||||||||||
Medical condition: Nonsquamous NSCLC that is Stage IIIB, Stage IV, or recurrent | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Completed) DK (Prematurely Ended) ES (Prematurely Ended) NL (Completed) PT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002773-10 | Sponsor Protocol Number: IRFMN-LUNG-8287 | Start Date*: 2022-03-14 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: A phase III prevention trial of canakinumab in subjects at high risk for lung cancer | ||||||||||||||||||
Medical condition: Subjects at high risk for lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000075-16 | Sponsor Protocol Number: BAY88-8223/16216 | Start Date*: 2012-06-20 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Radium-223 Dichloride (Alpharadin) in Castration-Resistant (Hormone-Refractory) Prostate Cancer Patients with Bone Metastasis | |||||||||||||
Medical condition: Castrate Resistant Prostate Cancer/Hormone-Refractory Prostate Cancer patients with bone metastasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) NO (Completed) FI (Completed) BE (Completed) ES (Completed) CZ (Completed) IE (Completed) GB (Completed) IT (Completed) DK (Prematurely Ended) NL (Completed) 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: 2011-003517-42 | Sponsor Protocol Number: SPI-1012 | Start Date*: 2011-11-23 | |||||||||||||||||||||
Sponsor Name:Spectrum Pharmaceuticals, Inc | |||||||||||||||||||||||
Full Title: A Phase 3 International, Multicenter, Double-Blind, Placebo-Controlled, Randomized Trial Evaluating the Efficacy and Safety of Multiple Instillations of Intravesical Apaziquone vs. Placebo in Patie... | |||||||||||||||||||||||
Medical condition: The medical condition under investigation is noninvasive bladder cancer in patients undergoing transurethral resection of bladder tumor/tumors. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Completed) CZ (Prematurely Ended) ES (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002192-33 | Sponsor Protocol Number: TRADEhypo | Start Date*: 2020-02-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: Thoracic Radiotherapy plus Durvalumab in Elderly and/or frail NSCLC stage III patients unfit for chemotherapy- Employing optimized (hypofractionated) radiotherapy to foster durvalumab efficacy | ||||||||||||||||||||||||||||||||||||||
Medical condition: unresectable stage III NSCLC (Non–small-cell lung cancer) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002605-25 | Sponsor Protocol Number: AIO-HEP-0120 | Start Date*: 2021-03-24 | |||||||||||||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||
Full Title: Neoadjuvant Bintrafusp alfa in patients with resectable biliary tract cancer (NEOBIL) | |||||||||||||||||||||||||||||||||
Medical condition: Treatment-naive subjects with a diagnosis of resectable biliary tract cancer, confirmed by histopathology | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-005090-13 | Sponsor Protocol Number: "Painstudy"1 | Start Date*: 2017-04-18 |
Sponsor Name:Cancer Registry of Norway | ||
Full Title: Reducing painful colonoscopies in women participating in a colorectal cancer screening program: A randomized controlled trial | ||
Medical condition: Many women are experiencing pain under colonoscopy. The present study aims to reduce pain in women undergoing colonoscopy in a bowel cancer screening program in Norway. | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
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