- Trials with a EudraCT protocol (1,048)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,048 result(s) found for: Recurrent or Metastatic Cancer AND Cancer.
Displaying page 24 of 53.
EudraCT Number: 2017-002824-26 | Sponsor Protocol Number: VHIO17001 | Start Date*: 2018-02-23 | |||||||||||
Sponsor Name:Vall d' Hebron Institute of Oncology (VHIO) | |||||||||||||
Full Title: Phase II trial of Pembrolizumab in combination with Doxorubicin in Advanced, Recurrent or Metastatic Endometrial Cancer (TOPIC) | |||||||||||||
Medical condition: Advanced, Recurrent or Metastatic Endometrial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (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: 2012-003757-28 | Sponsor Protocol Number: CRAD001Y2201 | Start Date*: 2013-02-20 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A three-arm, randomized, open label, phase II study of everolimus in combination with exemestane versus everolimus alone versus capecitabine in the treatment of postmenopausal women with estrogen r... | |||||||||||||
Medical condition: Estrogen receptor positive locally advanced or metastatic breast cancer in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) GB (Completed) IE (Completed) DK (Completed) ES (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003844-31 | Sponsor Protocol Number: H6Q-MC-S064 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Eli Lilly and Company limited | |||||||||||||
Full Title: A Double-Blind, Randomized, Placebo-Controlled, Phase 2 Study of Enzastaurin with 5 FU/LV plus Bevacizumab as Maintenance Regimen Following First Line Therapy for Metastatic Colorectal Cancer | |||||||||||||
Medical condition: Locally advanced or metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) IT (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005477-31 | Sponsor Protocol Number: I4C-MC-JTBC | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Open-Label Phase 2 Study Evaluating LY2875358 Plus Erlotinib and LY2875358 Monotherapy in MET Diagnostic Positive NSCLC Patients with Acquired Resistance to Erlotinib | |||||||||||||
Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) GB (Completed) BE (Completed) ES (Completed) NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005910-17 | Sponsor Protocol Number: KKSH176 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Phase 2 multicenter study investigating the tolerability and efficacy of UV1 vaccine in patients with recurrent or metastatic PD-L1 positive (CPS≥1) head and neck squamous cell carcinoma planned fo... | |||||||||||||
Medical condition: Recurrent or metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002472-34 | Sponsor Protocol Number: EGF109462 | Start Date*: 2007-08-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Limited | |||||||||||||
Full Title: A single-arm, two-stage Phase II study of Lapatinib and Pemetrexed in the second line treatment of advanced or metastatic Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: Patients with advanced or metatstatic Non-Small Cell Lung Cancer who have received one prior platinum containing chemotherapy regimen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003751-19 | Sponsor Protocol Number: PCIA202/10 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:PCI Biotech AS | |||||||||||||
Full Title: An open-label, single arm, multi-centre, Phase II study to evaluate the safety and efficacy of PC-A11 with superficial and interstitial laser light application in patients with recurrent head and n... | |||||||||||||
Medical condition: Recurrent head and neck squamous cell carcinoma (HNSCC) insuitable for surgery and radiotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) LT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000325-21 | Sponsor Protocol Number: A6181122 | Start Date*: 2007-05-02 | |||||||||||
Sponsor Name:Pfizer Inc. - 235 East 42nd Street - New York - 10017 | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PHASE 3 STUDY OF SUNITINIB IN METASTATIC COLORECTAL CANCER PATIENTS RECEIVING IRINOTECAN, 5-FLUOROURACIL AND LEUCOVORIN (FOLFIRI) AS FIRST LINE TREATMENT | |||||||||||||
Medical condition: first-line treatment of patients with metastatic colorectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) IE (Completed) DE (Completed) AT (Completed) ES (Completed) HU (Completed) BE (Completed) PT (Completed) CZ (Completed) GB (Completed) BG (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000309-21 | Sponsor Protocol Number: UCa-001 | Start Date*: 2018-10-31 | |||||||||||
Sponsor Name:Inovio Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open-Label, Multi-Center Trial of INO-5401 + INO-9012 in Combination with Atezolizumab in Subjects with Locally Advanced Unresectable or Metastatic/Recurrent Urothelial Carcinoma | |||||||||||||
Medical condition: Locally advanced unresectable or metastatic/recurrent Urothelial Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003636-36 | Sponsor Protocol Number: UCL/17/0396 | Start Date*: 2019-01-08 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: A phase II trial to assess the efficacy and safety profile of pembrolizumab in patients with performance status 2 with recurrent or metastatic squamous cell carcinoma of the head and neck | ||||||||||||||||||
Medical condition: Recurrent/metastatic head and neck squamous cell cancer | ||||||||||||||||||
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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: 2006-006459-10 | Sponsor Protocol Number: KU36-58 | Start Date*: 2007-07-18 | |||||||||||
Sponsor Name:KuDOS Pharmaceuticals Ltd. (a member of the AstraZeneca group of companies) | |||||||||||||
Full Title: A phase II, open-label, non-comparative, international, multicentre study to assess the efficacy and safety of KU 0059436 given orally twice daily in patients with advanced BRCA1- or BRCA2-associat... | |||||||||||||
Medical condition: Advanced ovarian cancer (stage IIIB/IIIC/IV) and confirmed BRCA+ status | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002124-21 | Sponsor Protocol Number: GINECO-EN105b | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:ARCAGY-GINECO | |||||||||||||
Full Title: Randomized phase III trial in MMR deficient endometrial cancer patients comparing chemotherapy alone versus Dostarlimab in first line advanced/metastatic setting: DOMENICA STUDY (GINECO-EN105b/ENGO... | |||||||||||||
Medical condition: Endometrial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004803-36 | Sponsor Protocol Number: 1199.13 | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||
Full Title: Multicentre, randomised, double-blind, Phase III trial to investigate the efficacy and safety of oral BIBF 1120 plus standard docetaxel therapy compared to placebo plus standard docetaxel therapy i... | |||||||||||||
Medical condition: stage IIIB/IV or recurrent non small cell lung cancer after failure of first line chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) CZ (Completed) AT (Completed) DK (Completed) LT (Completed) ES (Completed) SK (Completed) GB (Completed) FR (Completed) PT (Completed) BG (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014440-10 | Sponsor Protocol Number: EMR200068-006 | Start Date*: 2009-12-03 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A Phase II, Open-label, 1:1 Randomized, Controlled Trial Exploring the Efficacy of EMD 1201081 in Combination with Cetuximab in Second-Line Cetuximab-Naïve Subjects with Recurrent or Metastatic Squ... | |||||||||||||
Medical condition: Recurrent/metastatic squamous cell cancer of the head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) CZ (Prematurely Ended) HU (Completed) FR (Completed) SK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001892-35 | Sponsor Protocol Number: MK-7339-009 | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc | |||||||||||||
Full Title: An Open-label, Randomized, Phase 2/3 Study of Olaparib Plus Pembrolizumab Versus Chemotherapy Plus Pembrolizumab After Induction of Clinical Benefit With First-line Chemotherapy Plus Pembrolizumab ... | |||||||||||||
Medical condition: Locally Recurrent Inoperable or Metastatic Triple Negative Breast Cancer (TNBC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Trial now transitioned) HU (Trial now transitioned) IE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022240-21 | Sponsor Protocol Number: ISIS183750-CS4 | Start Date*: 2011-04-29 | |||||||||||
Sponsor Name:Isis Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 1b/2 Study of Carboplatin-Paclitaxel, with or without ISIS 183750 (an eIF4E Inhibitor), in Patients with Stage IV Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: Stage IV Non-Small Cell Lung Cancer (NSCLC; including patients with pleural effusion who were previously classified as Stage IIIB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002164-13 | Sponsor Protocol Number: UZBRU_VHH1_3 | Start Date*: 2017-01-05 |
Sponsor Name:UZ Brussel | ||
Full Title: Quantification of 68GaNOTA-Anti-HER2 VHH1 Uptake in metastasis of Breast carcinoma and cancer patients and Assessment of Repeatability – Pilot study | ||
Medical condition: Breast cancer; salivary gland cancer; adenocarcinoma of the gastric body or gastro-esophageal junction; endometrial cancer; cancer of cervix uteri; Non-small cell lung cancer; biliary tract cancer;... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004627-33 | Sponsor Protocol Number: GSN000400 | Start Date*: 2022-02-03 | |||||||||||
Sponsor Name:Genkyotex Suisse SA | |||||||||||||
Full Title: A Phase 2, Randomised, Double-Blind, Placebo-Controlled, Proof-of-Concept Study to Evaluate the Efficacy, Safety, and Tolerability, and Effects on Tumour Biomarkers of the NOX1/4 Inhibitor Setanaxi... | |||||||||||||
Medical condition: Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck (SCCHN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002030-36 | Sponsor Protocol Number: CA2097DX | Start Date*: 2019-11-26 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind Study of Nivolumab or Placebo in Combination with Docetaxel, in Men with Metastatic Castration-resistant Prostate Cancer | ||||||||||||||||||
Medical condition: Metastatic Castration-resistant Prostate Cancer (mCRPC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) DE (Completed) FR (Completed) BE (Completed) CZ (Completed) IT (Completed) RO (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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