- Trials with a EudraCT protocol (512)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
512 result(s) found for: Kidney Cancer AND Cancer.
Displaying page 17 of 26.
EudraCT Number: 2019-004074-25 | Sponsor Protocol Number: ABc2 | Start Date*: 2020-08-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: A Phase II Open-Label Randomized COntrolled Pre-Surgical Feasibility Study of Antibiotic COmbinations in Early Breast Cancer | |||||||||||||
Medical condition: We investigated, in a population of patients with breast cancer, the combined effect of azithrocyn, docyciclin and vitamin C on biomarkers associated with cell proliferation | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003947-31 | Sponsor Protocol Number: | Start Date*: 2016-12-30 | |||||||||||
Sponsor Name:Oxford University Hospitals NHS Trust | |||||||||||||
Full Title: Optimising Renal outcome in Myeloma renal failure A pilot study of Thalidomide, Bendamustine, and Dexamethasone (TBD) vs Bortezomib, Bendamustine, and Dexamethasone (BBD) in patients with renal fa... | |||||||||||||
Medical condition: Myeloma and renal impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004840-30 | Sponsor Protocol Number: PrepDial | Start Date*: 2020-11-04 | |||||||||||
Sponsor Name:Policlinico di Bari-UO Gastroenterologia | |||||||||||||
Full Title: Comparison of low-volume versus high-volume polyethylene glycol based bowel preparation for colonoscopy in people receiving hemodialysis: a randomized non-inferiority trial. | |||||||||||||
Medical condition: Colonoscopy in people receiving hemodialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000348-77 | Sponsor Protocol Number: XL184-315 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:Exelixis, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Open-Label, Controlled Study of Cabozantinib (XL184) in Combination with Atezolizumab vs Second Novel Hormonal Therapy (NHT) in Subjects with Metastatic Castration-Resistant ... | |||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) PT (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) AT (Completed) GR (Trial now transitioned) CZ (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006370-25 | Sponsor Protocol Number: IMA901-202 | Start Date*: 2007-05-07 |
Sponsor Name:immatics biotechnologies GmbH | ||
Full Title: Phase 2, randomised, open label, multicenter study of intradermal IMA901 plus GM-CSF with or without low dose cyclophosphamide pre-treatment in advanced renal cell carcinoma patients with measurabl... | ||
Medical condition: HLA-A*02-positive patients with advanced clear cell RCC who have progressed during or after first-line systemic therapy for advanced disease and have a favourable or intermediate risk after systemi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) SK (Completed) GB (Completed) AT (Completed) HU (Completed) ES (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004727-31 | Sponsor Protocol Number: IRST100.26 | Start Date*: 2016-03-16 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | |||||||||||||
Full Title: RANDOMIZED PHASE II TRIAL IN SSTr2 POSITIVE TUMORS TO OPTIMIZE THE INTERVAL BETWEEN CYCLES OF PRRT WITH 177LU DOTATATE (LUTHREE) | |||||||||||||
Medical condition: SSTr2 POSITIVE TUMORS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003779-20 | Sponsor Protocol Number: SCO101-001 | Start Date*: 2020-01-28 | |||||||||||
Sponsor Name:Scandion Oncology A/S | |||||||||||||
Full Title: An open-label phase II prospective clinical trial to investigate safety, tolerability, maximum tolerated dose and anti-tumor effect for SCO-101 in combination with FOLFIRI as a safe and efficient t... | |||||||||||||
Medical condition: Metastatic or advanced colorectal cancer (mCRC) with acquired resistance to chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000049-30 | Sponsor Protocol Number: RITE-2 | Start Date*: 2017-07-26 |
Sponsor Name:Medical Enterprises Europe B.V | ||
Full Title: A multicenter, single-arm study evaluating the efficacy of Synergo radiofrequency-induced thermochemotherapy effect (RITE) with Mitomycin C( Synergo + MMC) in non-muscle invasive bladder cancer (NM... | ||
Medical condition: Non-Muscle-Invasive Bladder Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001356-37 | Sponsor Protocol Number: NSGO-CC-0304 | Start Date*: 2004-09-10 |
Sponsor Name:Nordic Society for Gynecological Cancer | ||
Full Title: Phase I-II-III studies of Cisplatin and Combretastatin (CA4P) in recurrent or advanced servical cancer | ||
Medical condition: Metastatic or recurrent cervical cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002470-23 | Sponsor Protocol Number: 2011-002470-23 | Start Date*: 2011-06-09 | |||||||||||||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO MEDITERRANEO NEUROMED | |||||||||||||||||||||||
Full Title: Evaluation of diagnosic accuracy of 18F-choline PET/CT in examination of patients qith prostate cancer, in relation to PSA value and its derivatives. | |||||||||||||||||||||||
Medical condition: Patients with prostate cancer histologically proved | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002582-15 | Sponsor Protocol Number: NerHer-1 | Start Date*: 2023-03-20 |
Sponsor Name:Medical University Graz | ||
Full Title: Phase II Study of Neratinib and Trastuzumab +/- Vinorelbine p.o. in Pre-treated Metastatic HER2-positive Breast Cancer (Ner-Her-1) | ||
Medical condition: Patients with histologically confirmed Human Epidermal Growth Factor Receptor 2 (HER2)-positive metastatic breast cancer (mBC) pretreated with trastuzumab, pertuzumab, and/or trastuzumab emtansine... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-003436-13 | Sponsor Protocol Number: 105RC101 | Start Date*: 2016-05-24 | |||||||||||
Sponsor Name:TRACON Pharmaceuticals, Inc. | |||||||||||||
Full Title: A RANDOMIZED PHASE 2 TRIAL OF AXITINIB AND TRC105 VERSUS AXITINIB ALONE (INCLUDING A LEAD-IN PHASE 1B DOSE-ESCALATION PORTION) IN PATIENTS WITH ADVANCED OR METASTATIC RENAL CELL CARCINOMA | |||||||||||||
Medical condition: ADVANCED OR METASTATIC RENAL CELL CARCINOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Prematurely Ended) PL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007786-23 | Sponsor Protocol Number: A4061046 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: ESTUDIO EN FASE 2 ALEATORIZADO Y DOBLE CIEGO DE AXITINIB (AG-013736) CON O SIN AJUSTE DE LA DOSIS EN PACIENTES CON CANCER DE CELULAS RENALES METASTASICO RANDOMIZED, DOUBLE-BLIND PHASE 2 STUDY OF A... | |||||||||||||
Medical condition: CCR metastásico Metastatic RCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001881-27 | Sponsor Protocol Number: WO39210 | Start Date*: 2017-03-01 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase III, multicenter, randomized, placebo-controlled, double-blind study of atezolizumab (anti-PD-L1 antibody) as adjuvant therapy in patients with renal cell carcinoma at high risk of developi... | |||||||||||||
Medical condition: Patients at high risk of Renal Cell Carcinoma (RCC) recurrence after nephrectomy and select patients with metastatic RCC recurrence who have undergone complete metastasectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) NL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) CZ (Completed) BE (Completed) PL (Completed) ES (Completed) IE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005939-78 | Sponsor Protocol Number: C-II-008 | Start Date*: 2012-06-25 | |||||||||||
Sponsor Name:CESAR Central European Society for Anticancer Drug Research-EWIV | |||||||||||||
Full Title: A prospective, open-label, multicenter, randomized phase II trial: Sequential therapy with BEvacizumab, RAd001 (everolimus) and AxiTinib in metastatic renal cell carcinoma (mRCC) (BERAT study) | |||||||||||||
Medical condition: metastatic renal cell carcinoma (mRCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004111-32 | Sponsor Protocol Number: OTRAPAC | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: Prospective, open-label, multicentre study on the incidence of Squamous Cell Carcinoma and Actinic Keratoses in solid organ transplant recipients treated with per protocol, cyclic field application... | |||||||||||||
Medical condition: Squamous Cell Carcinoma and Actinic Keratoses in solid organ transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000528-17 | Sponsor Protocol Number: IAEA-HypoX | Start Date*: 2012-06-05 |
Sponsor Name:Department of Experimental Clinical Oncology | ||
Full Title: A randomized multicenter study of accelerated fractionated radiotherapy with or without the hypoxic radiosensitizer nimorazole in the treatment of squamous cell carcinoma of the head and neck | ||
Medical condition: Squamous Cell Carcinoma of the Head and Neck region | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SI (Completed) EE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002351-26 | Sponsor Protocol Number: CA209-238 | Start Date*: 2015-03-18 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind Study of Adjuvant Immunotherapy with Nivolumab versus Ipilimumab after Complete Resection of Stage IIIb/c or Stage IV Melanoma in Subjects who are at High Risk f... | |||||||||||||
Medical condition: High risk, completely resected Stage IIIb/c and IV melanoma subjects. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IE (Completed) GB (GB - no longer in EU/EEA) NO (Completed) FI (Completed) SE (Completed) CZ (Completed) ES (Ongoing) AT (Completed) NL (Completed) FR (Completed) HU (Completed) GR (Completed) PL (Completed) RO (Ongoing) Outside EU/EEA IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001096-20 | Sponsor Protocol Number: 1169/2013 | Start Date*: 2014-02-19 |
Sponsor Name:Department of Molecular and Clinical Medicine; "Sapienza" University of Rome | ||
Full Title: ASSOCIATION BETWEEN PROTON-PUMP INHIBITORS (PPI) and METRONOMIC CAPECITABINE (mCAP) AS SALVAGE TREATMENT FOR PATIENTS WITH ADVANCED GASTRO-INTESTINAL TUMOURS: A RANDOMIZED PHASE II STUDY | ||
Medical condition: Patients with gastrointestinal malignancies ineligible for conventional chemotherapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001823-15 | Sponsor Protocol Number: 20CH089 | Start Date*: 2020-04-28 | ||||||||||||||||
Sponsor Name:CHU de Saint Etienne | ||||||||||||||||||
Full Title: Evaluation of the concentration-effect relationship of enoxaparin for thromboembolic prevention in COVID-19 resuscitation patients. COV-ENOX study | ||||||||||||||||||
Medical condition: covid-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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