- Trials with a EudraCT protocol (4,805)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4,805 result(s) found for: Carcinoma.
Displaying page 43 of 241.
| EudraCT Number: 2020-000556-35 | Sponsor Protocol Number: D910LC00001 | Start Date*: 2020-12-01 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase III, Randomized, Multicenter, Double-blind, Placebo-controlled Study to Determine the Efficacy of Adjuvant Durvalumab in Combination with Platinum-based Chemotherapy in Completely Resected ... | |||||||||||||
| Medical condition: Completely Resected Stage II-III NSCLC | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) NL (Prematurely Ended) DK (Prematurely Ended) BG (Completed) HU (Prematurely Ended) DE (Completed) BE (Completed) SE (Prematurely Ended) PL (Completed) CZ (Completed) GR (Completed) IT (Prematurely Ended) FR (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-003695-35 | Sponsor Protocol Number: D4200C00036 | Start Date*: 2007-01-24 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase III, Randomized, Double-blinded, Parallel Group, Multi-centre Study to Assess the Efficacy and Safety of ZD6474 (ZACTIMA™) in Combination with Pemetrexed (Alimta®) versus Pemetrexed alone i... | |||||||||||||
| Medical condition: Locally-advanced or Metastatic (stage IIIB or IV) Non-Small Cell Lung Cancer (NSCLC). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) GR (Ongoing) PT (Completed) IT (Completed) BE (Completed) GB (Completed) ES (Completed) FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002925-31 | Sponsor Protocol Number: GO41717 | Start Date*: 2020-05-18 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLINDED, PLACEBO-CONTROLLED STUDY OF TIRAGOLUMAB, AN ANTI-TIGIT ANTIBODY, IN COMBINATION WITH ATEZOLIZUMAB COMPARED WITH PLACEBO IN COMBINATION WITH ATEZOLIZUMAB IN ... | ||||||||||||||||||
| Medical condition: Non-small cell lung cancer (NSCLC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) DK (Prematurely Ended) PL (Trial now transitioned) HU (Trial now transitioned) AT (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-005427-16 | Sponsor Protocol Number: D4191C00003 | Start Date*: 2014-07-22 | ||||||||||||||||
| Sponsor Name:AstraZeneca AB | ||||||||||||||||||
| Full Title: A Phase II, Non-comparative, Open label, Multi-centre, International Study of MEDI4736, in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (Stage IIIB-IV) who have receive... | ||||||||||||||||||
| Medical condition: Locally Advanced or Metastatic Non-Small Cell Lung Cancer (Stage IIIB-IV) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) CZ (Completed) DE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) BE (Trial now transitioned) AT (Completed) ES (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-000272-34 | Sponsor Protocol Number: L00070-IN-214-P1 | Start Date*: 2011-08-29 | |||||||||||
| Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
| Full Title: Phase II study assessing the maintenance treatment with vinflunine after first-line therapy with gemcitabine and cisplatin in patients with advanced or metastatic transitional cell carcinoma of the... | |||||||||||||
| Medical condition: Advanced or metastatic predominantly transitional cell carcinoma of the urothelial tract. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001249-15 | Sponsor Protocol Number: 314-12-401 | Start Date*: 2013-11-07 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Otsuka Novel Products GmbH | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Two-Part Phase 1/2a, Open-Label, Dose-Escalation Study to Evaluate the Tolerability and Preliminary Antitumour Activity of OPB-111001 in Patients with Advanced Cancers that are Poorly Responsive ... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: • Advanced prostate cancer • Advanced epithelial ovarian cancer, advanced squamous cell carcinoma of the cervix, advanced breast cancer, endometrial cancer, and salivary gland cancer that are p... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2009-016853-16 | Sponsor Protocol Number: MGN1601-CT1 | Start Date*: 2010-08-31 | |||||||||||
| Sponsor Name:MOLOGEN AG | |||||||||||||
| Full Title: A Phase I/II, Proof-of-Principle, Multi-Center, Open-Label, Single-Arm, Non-randomized Clinical Study to Assess Safety and Efficacy of a Tumor Vaccine Consisting of Genetically Modified Allogeneic ... | |||||||||||||
| Medical condition: Advanced renal cell carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000989-23 | Sponsor Protocol Number: D4881C00024 | Start Date*: 2008-07-01 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A ROLLOVER PROTOCOL FOR PATIENTS WHO RECEIVED TREMELIMUMAB (CP-675,206) IN OTHER PROTOCOLS | |||||||||||||
| Medical condition: Patients who have / have had Melanoma and Other Tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005136-34 | Sponsor Protocol Number: THIO101 | Start Date*: 2022-11-16 | |||||||||||||||||||||
| Sponsor Name:MAIA Biotechnology, Inc. | |||||||||||||||||||||||
| Full Title: A Multicenter, Open-Label, Dose-Finding, Phase 2 Study Evaluating THIO Sequenced with Cemiplimab (LIBTAYO®) in Subjects with Advanced Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||
| Medical condition: Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BG (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2007-001890-27 | Sponsor Protocol Number: D4200C00079 | Start Date*: 2007-06-15 | |||||||||||
| Sponsor Name:AstraZeneca SAS | |||||||||||||
| Full Title: A Randomized, Double Blind, placebo-controlled Phase II, Multi-Centre Study to Assess the Efficacy and Safety of Zactima™ in Patients with advanced or metastatic papillary or follicular Thyroid Car... | |||||||||||||
| Medical condition: Advanced or metastatic papillary or follicular Thyroid Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) DK (Completed) SE (Completed) ES (Ongoing) BE (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005771-12 | Sponsor Protocol Number: AIO-KRK-0420 | Start Date*: 2022-05-30 | ||||||||||||||||||||||||||
| Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||||||||||||
| Full Title: Neoadjuvant encorafenib, binimetinib and cetuximab for patients with BRAF V600E mutated/pMMR localized colorectal cancer | ||||||||||||||||||||||||||||
| Medical condition: Patients with unresected BRAFV600E mutated/pMMR localized colorectal cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-002133-22 | Sponsor Protocol Number: C31005 | Start Date*: 2016-05-29 | ||||||||||||||||
| Sponsor Name:Millenium Pharmaceuticals, a wholly owned subsidiary of Takeda pharmaceutical Company Limited | ||||||||||||||||||
| Full Title: A Phase 2, Open-label Study to Evaluate the Efficacy and Safety of Single-Agent MLN0128 and the Combination of MLN0128+MLN1117 Compared With Everolimus in the Treatment of Adult Patients With Advan... | ||||||||||||||||||
| Medical condition: metastatic clear-cell renal cell carcinoma (mccRCC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) FR (Completed) PL (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-019525-34 | Sponsor Protocol Number: MO22923 | Start Date*: 2010-12-17 | |||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
| Full Title: GLOBAL STUDY TO ASSESS THE ADDITION OF BEVACIZUMAB TO CARBOPLATIN AND PACLITAXEL AS FRONT-LINE TREATMENT OF EPITHELIAL OVARIAN CANCER, FALLOPIAN TUBE CARCINOMA OR PRIMARY PERITONEAL CARCINOMA | |||||||||||||||||||||||
| Medical condition: EPITHELIAL OVARIAN CANCER FALLOPIAN TUBE CARCINOMA PRIMARY PERITONEAL CARCINOMA | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: SK (Completed) FR (Completed) ES (Completed) LT (Completed) AT (Completed) LV (Completed) NL (Completed) IE (Completed) SE (Completed) EE (Completed) HU (Completed) IT (Completed) BG (Completed) DK (Completed) SI (Completed) GR (Completed) PT (Completed) PL (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-003399-36 | Sponsor Protocol Number: MK-4214-008 | Start Date*: 2011-10-28 | |||||||||||||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
| Full Title: A Phase III Randomized, Double-Blind, Active-Controlled Clinical Trial to Study the Efficacy and Safety of MK-4214 (filgrastim) and Neupogen™ as an Adjunct to Combination Chemotherapy with Doxorubi... | |||||||||||||||||||||||
| Medical condition: Breast Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-003026-69 | Sponsor Protocol Number: IO102-IO103-022 | Start Date*: 2022-05-09 | |||||||||||||||||||||
| Sponsor Name:IO Biotech ApS | |||||||||||||||||||||||
| Full Title: A Phase II Multi-Arm (basket) Trial Investigating the Safety and Efficacy of IO102-IO103 in Combination with Pembrolizumab, as First-line Treatment for Patients with Metastatic Non-Small Cell Lung ... | |||||||||||||||||||||||
| Medical condition: Metastatic Non-Small Cell Lung Cancer (NSCLC), Metastatic Squamous Cell Carcinoma of Head and Neck (SCCHN), Metastatic Urothelial Bladder Cancer (mUBC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2008-000332-40 | Sponsor Protocol Number: TTCC-2007-02 | Start Date*: 2008-05-21 | |||||||||||
| Sponsor Name:GRUPO ESPAÑOL DE TRATAMIENTO DE TUMORES DE CABEZA Y CUELLO (TTCC) | |||||||||||||
| Full Title: ESTUDIO FASE II CON RADIOTERAPIA (RT) CONVENCIONAL + CETUXIMAB PARA EVALUAR LA SUPERVIVENCIA ESPECÍFICA LIBRE DE LARINGECTOMIA TOTAL EN PACIENTES AFECTOS DE UN CARCINOMA ESCAMOSO DE LARINGE LOCALME... | |||||||||||||
| Medical condition: CARCINOMA ESCAMOSO DE LARINGE LOCALMENTE AVANZADO RESECABLE | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006790-81 | Sponsor Protocol Number: APREC S2007-01 | Start Date*: 2008-07-28 | ||||||||||||||||
| Sponsor Name:APREC | ||||||||||||||||||
| Full Title: Phase II study of pegylated liposomal doxorubicin (Caelyxâ) in breast cancer patients with brain metastases and not candidate for an antiHER2 therapy | ||||||||||||||||||
| Medical condition: Breast Cancer Patients with Brain Metastases | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-003673-42 | Sponsor Protocol Number: MM-121-01-02-09 | Start Date*: 2016-01-19 | ||||||||||||||||
| Sponsor Name:Merrimack Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: SHERLOC: A Phase 2 Study of MM-121 in Combination with Docetaxel versus Docetaxel Alone in Patients with Heregulin Positive, Locally Advanced or Metastatic Non-Small Cell Lung Cancer | ||||||||||||||||||
| Medical condition: Heregulin Positive, Locally Advanced or Metastatic Non-Small Cell Lung Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-001077-14 | Sponsor Protocol Number: 1200.217 | Start Date*: 2014-12-17 | ||||||||||||||||||||||||||
| Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | ||||||||||||||||||||||||||||
| Full Title: An open label, single-arm phase IV study to assess the efficacy and safety of afatinib as second-line therapy for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) har... | ||||||||||||||||||||||||||||
| Medical condition: Metastatic non-small cell lung cancer harbouring an EGFR mutation (Del 19 or L858R) | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: RO (Completed) PL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-005887-24 | Sponsor Protocol Number: GEMCAD-2103//MO44170 | Start Date*: 2022-11-25 | |||||||||||
| Sponsor Name:Grupo Español Multidisciplinar de Cáncer Digestivo (GEMCAD) | |||||||||||||
| Full Title: Phase II study of Atezolizumab plus Tiraglolumab in combination with chemoradiotherapy in localized squamous cell carcinoma of the anal canal | |||||||||||||
| Medical condition: Locallized squamous cell carcinoma of the anal canal in the first-line setting. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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