- Trials with a EudraCT protocol (6,808)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (555)
6,808 result(s) found for: Tumor.
Displaying page 108 of 341.
EudraCT Number: 2021-003751-42 | Sponsor Protocol Number: ICH-013-UroNEOadI | Start Date*: 2022-01-25 | |||||||||||
Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Randomized phase III clinical trial of Neo-Adjuvant Intravesical mitomycin C (MMC) treatment in patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
Medical condition: Patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016782-28 | Sponsor Protocol Number: GMIHO-009/2009/AG52 | Start Date*: 2010-09-15 | ||||||||||||||||
Sponsor Name:GMIHO Gesellschaft für Medizinische Innovation - Hämatologie und Onkologie mbH | ||||||||||||||||||
Full Title: Panitumimab in combination with radiotherapy in patients with locally advanced RAS wildtype rectal cancer (clinical stages II and III) | ||||||||||||||||||
Medical condition: Locally advanced RAS wildtype rectal cancer (clinical stage II and III) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002625-35 | Sponsor Protocol Number: CALGB80802 | Start Date*: 2013-09-23 |
Sponsor Name:All Ireland Co-operative Oncology Research Group (ICORG) | ||
Full Title: Phase III Randomized Study Of Sorafenib Plus Doxorubicin Versus Sorafenib In Patients With Advanced Hepatocellular Carcinoma (HCC) | ||
Medical condition: Advanced or Metastatic Hepatocellular Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004608-22 | Sponsor Protocol Number: 17-PP-21 | Start Date*: 2018-05-22 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Open, prospective, single-center study evaluating the efficacy and safety of 0.05% ingénol mebutate (Picato® 500) in the treatment of basal cell carcinoma Study "PICABAS" | |||||||||||||
Medical condition: Patients with one or more basal cell carcinoma superficial, or nodular, trunk or limb | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002156-14 | Sponsor Protocol Number: OCS–3rdLINE/OCCASIONE-STUDY | Start Date*: 2008-09-17 | |||||||||||
Sponsor Name:FUNDATION OF EXPERIMENTAL AND CLINICAL ONCOLOGY | |||||||||||||
Full Title: A phase II non-randomised, open-label, single-arm study to assess the efficacy, safety and tolerability of Nexavar ® (Sorafenib) monotherapy as third line therapy in patients with progressed ovaria... | |||||||||||||
Medical condition: 1. progressed ovarian epithelial cancer 2. primary peritoneal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000105-20 | Sponsor Protocol Number: 0316-ASG | Start Date*: 2017-10-02 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: Neoadjuvant anti PD-1 immunotherapy in resectable non-small cell lung cancer | ||||||||||||||||||
Medical condition: non-small cell lung cancer (NSCLC), resectable | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002449-13 | Sponsor Protocol Number: S65525 | Start Date*: 2021-07-30 | |||||||||||
Sponsor Name:University Hospitals Leuven (UZ Leuven) | |||||||||||||
Full Title: Visualisation of Indocyanine Green in Primary and Interval Debulking for Ovarian Cancer | |||||||||||||
Medical condition: Advanced stage high-grade serous epithelial ovarian cancer: FIGO stage IIIb, IIIc and IV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000921-61 | Sponsor Protocol Number: NONK-3/NOA-12 | Start Date*: 2012-04-25 | ||||||||||||||||
Sponsor Name:Ruprecht-Karls-University Heidelberg, Medical Faculty | ||||||||||||||||||
Full Title: A phase I/II, randomized, open-label, multi-centre study of BIBF1120 + reirradiation (R-RT) versus reirradiation in the treatment of patients with first or second progression of glioblastoma | ||||||||||||||||||
Medical condition: glioblastoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002206-20 | Sponsor Protocol Number: MK-3475-052 | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase II Clinical Trial of Pembrolizumab (MK-3475) in Subjects with Advanced/Unresectable or Metastatic Urothelial Cancer | |||||||||||||
Medical condition: advanced/unresectable (inoperable) or metastatic urothelial cancer of the renal pelvis, ureter, bladder, or urethra. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Completed) IT (Completed) IE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001537-24 | Sponsor Protocol Number: EMR100070-005 | Start Date*: 2015-12-14 | |||||||||||||||||||||
Sponsor Name:Merck KGaA | |||||||||||||||||||||||
Full Title: A Phase III, open-label, multicenter trial of avelumab (MSB0010718C) versus platinum based doublet as a first line treatment of recurrent or Stage IV PD L1+ non small cell lung cancer | |||||||||||||||||||||||
Medical condition: First Line Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) DE (Completed) PT (Completed) LT (Completed) BE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) ES (Temporarily Halted) HU (Completed) PL (Completed) NL (Completed) FR (Completed) DK (Completed) BG (Completed) HR (Completed) CY (Completed) GR (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001080-36 | Sponsor Protocol Number: 20150195 | Start Date*: 2016-11-17 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Amgen Incorporated | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1b/2 Study Assessing Safety and Anti-tumor Activity of AMG 820 in Combination With Pembrolizumab in Select Advanced Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced Colorectal cancer (CRC), pancreatic cancer or non-small cell lung cancer (NSCLC), and other indications dependent on emerging data | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002807-24 | Sponsor Protocol Number: CA018-003 | Start Date*: 2017-08-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2, Fast Real-time Assessment of Combination Therapies in Immuno-ONcology Study in Participants with Advanced Gastric Cancer - Master Revprot05 dated 13-Sep-2019 - Sub-protocol A Revpro... | |||||||||||||
Medical condition: Advanced Gastric Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002481-13 | Sponsor Protocol Number: AG881-C-004 | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-Controlled Study of AG-881 in Subjects With Residual or Recurrent Grade 2 Glioma With an IDH1 or IDH2 Mutation | |||||||||||||
Medical condition: Residual or Recurrent Grade 2 Glioma With an IDH1 or IDH2 Mutation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004076-34 | Sponsor Protocol Number: 7487-CL-0209 | Start Date*: 2014-02-27 | ||||||||||||||||||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | ||||||||||||||||||||||||||||
Full Title: A phase II open-label rollover study for subjects that have participated in an Astellas sponsored linsitinib trial | ||||||||||||||||||||||||||||
Medical condition: Solid tumors | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003929-22 | Sponsor Protocol Number: ICON7 | Start Date*: 2006-12-15 | |||||||||||
Sponsor Name:Medical Research Council | |||||||||||||
Full Title: ICON7 - A randomised, two-arm, multicentre Gynaecologic Cancer InterGroup trial of adding bevacizumab to standard chemotherapy (carboplatin and paclitaxel) in patients with epithelial ovarian cancer. | |||||||||||||
Medical condition: Following initial surgery (either debulking cytoreductive surgery or a biopsy if the patient has FIGO stage IV disease and there is no planned surgery before disease progression) patients with new... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) DE (Completed) DK (Completed) SE (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016468-35 | Sponsor Protocol Number: D8480C00067 | Start Date*: 2016-03-29 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, phase III efficacy and safety study of cediranib (RECENTIN™ ) when added to cisplatin plus a fluoropyrimidine, compared with cisplatin plus a fluoropyrimidine alone, in ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Gastric cancer | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GR (Completed) HU (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015970-36 | Sponsor Protocol Number: D0810C00041 | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Open-Label, Randomised, Comparative, Multicentre Study to Compare the Efficacy and tolerability of Oral Olaparib in combination with Carboplatin and Paclitaxel Versus Carboplatin and Pa... | |||||||||||||
Medical condition: Serous ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) DE (Completed) CZ (Completed) BE (Completed) ES (Ongoing) IT (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003652-32 | Sponsor Protocol Number: ISA101b-OPC-03-19 | Start Date*: 2021-04-13 | |||||||||||
Sponsor Name:ISA Therapeutics B.V. | |||||||||||||
Full Title: A Phase II Study of cemiplimab, an anti-PD-1 monoclonal antibody, and ISA101b vaccine in patients with recurrent/metastatic HPV16- positive Oropharyngeal Cancer who have experienced disease progres... | |||||||||||||
Medical condition: Recurrent/metastatic HPV16- positive Oropharyngeal Cancer (OPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) BE (Completed) CZ (Completed) ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000125-27 | Sponsor Protocol Number: EORTC-1976-STBSG-QLG-ETF | Start Date*: 2022-05-31 |
Sponsor Name:EORTC AISBL/IVZW | ||
Full Title: TOLERANCE: a 3 arm randomized study on healTh-related quality Of Life of EldeRly pAtients with advaNced soft tissue sarComa undergoing doxorubicin every three weeks or doxorubicin weekly or cycloph... | ||
Medical condition: Advanced/metastatic soft tissue sarcoma | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) NL (Completed) CY (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-002669-38 | Sponsor Protocol Number: 0822-016 | Start Date*: 2006-12-07 | |||||||||||
Sponsor Name:Merck & Co Inc. | |||||||||||||
Full Title: A Phase II Study to Assess the Safety, Tolerability, and Efficacy of MK-0822 (Cathepsin-K Inhibitor) in the Treatment of Women with Breast Cancer and Established Bone Metastases (MBD) | |||||||||||||
Medical condition: Metastatic Bone Disease (MBD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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