- Trials with a EudraCT protocol (111)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
111 result(s) found for: Radiation monitoring.
Displaying page 1 of 6.
EudraCT Number: 2018-004490-27 | Sponsor Protocol Number: 18POUM06 | Start Date*: 2019-09-11 | |||||||||||
Sponsor Name:INSTITUT CLAUDIUS REGAUD | |||||||||||||
Full Title: A multicentric Phase II, open-label study evaluating the efficacy of the combination of hypofractionated stereotactic radiation therapy with the anti-PDL1 immune checkpoint inhibitor Durvalumab in ... | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001709-25 | Sponsor Protocol Number: CCR5119 | Start Date*: 2020-02-06 |
Sponsor Name:The Institute of Cancer Research | ||
Full Title: Randomised phase II trial testing efficacy of intra-tumoural hydrogen peroxide as a radiation sensitiser in patients with locally advanced/recurrent breast cancer | ||
Medical condition: Patients with locally advanced/recurrent breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003680-25 | Sponsor Protocol Number: CNAO_44-2021C_ICONIC | Start Date*: 2021-12-14 | ||||||||||||||||
Sponsor Name:Fondazione CNAO Centro Nazionale di Adroterapia Oncologica | ||||||||||||||||||
Full Title: Immune checkpoint inhibitors and Carbon iON radiotherapy In solid Cancers with stable disease (ICONIC) | ||||||||||||||||||
Medical condition: • Unresectable or metastatic melanoma • Locally advanced or metastatic non-small cell lung cancer (NSCLC) • Untreated recurrent/metastatic head & neck sqamous cell carcinoma (HNSC... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006421-13 | Sponsor Protocol Number: BBD | Start Date*: 2008-11-28 |
Sponsor Name:Wilhelminen Krebsforschung GmbH | ||
Full Title: Multicenter Phase II Study: Bendamustine plus Bortezomib plus Dexamethasone in the treatment of stage II/III relapsed or refractory multiple myeloma | ||
Medical condition: Patients suffering from stage II/III (Salmon & Durie) relapsed or refractory multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000864-42 | Sponsor Protocol Number: IFX-1-P2.8 | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:InflaRx GmbH | |||||||||||||
Full Title: OPEN LABEL, MULTICENTER PHASE II STUDY OF THE C5A-ANTIBODY IFX-1 ALONE OR IFX-1 + PEMBROLIZUMAB IN PATIENTS WITH PD-1- OR PD-L1-RESISTANT/REFRACTORY LOCALLY ADVANCED OR METASTATIC CUTANEOUS SQUAMOU... | |||||||||||||
Medical condition: Locally advanced or metastatic cutaneous squamous cell carcinoma (cSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003582-28 | Sponsor Protocol Number: LOXO-TRK-15002 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bayer Consumer Care AG | |||||||||||||
Full Title: A Phase 2 Basket Study of the Oral TRK Inhibitor larotrectinib in Subjects with NTRK Fusion-Positive Tumors | |||||||||||||
Medical condition: Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Trial now transitioned) IE (Completed) ES (Trial now transitioned) PT (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) SE (Trial now transitioned) BE (Completed) CZ (Completed) SK (Completed) NO (Completed) HU (Completed) PL (Completed) GR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002066-24 | Sponsor Protocol Number: PrE0204 | Start Date*: 2015-08-28 |
Sponsor Name:The All Ireland Cooperative Oncology Research Group (ICORG) | ||
Full Title: A Multi-Institutional, Single Arm, Two-Stage Phase II Trial of Nab-Paclitaxel and Gemcitabine for First-Line Treatment of Patients with Advanced or Metastatic Cholangiocarcinoma | ||
Medical condition: Advanced or metastatic cholangiocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002054-39 | Sponsor Protocol Number: ODX-002 | Start Date*: 2014-11-10 | |||||||||||
Sponsor Name:DexTech Medical AB | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled multi-centre phase II study to evaluate efficacy and tolerability of ODX (Osteodex) in Metastatic Castration Resistant Prostate Cancer (CRPC) | |||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer (CRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004053-88 | Sponsor Protocol Number: EuroNet-PHL-C2 | Start Date*: 2015-07-01 |
Sponsor Name:Justus-Liebig-University Giessen | ||
Full Title: EuroNet-Paediatric Hodgkin’s Lymphoma Group Second International Inter-Group Study for Classical Hodgkin’s Lymphoma in Children and Adolescents | ||
Medical condition: Hodgkin lymphoma in children and adolescents | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) AT (Completed) CZ (Completed) ES (Ongoing) IT (Prematurely Ended) NL (Completed) DK (Prematurely Ended) FR (Ongoing) PL (Prematurely Ended) FI (Completed) GB (GB - no longer in EU/EEA) SE (Completed) NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021070-11 | Sponsor Protocol Number: 005/05E | Start Date*: 2010-11-23 |
Sponsor Name:BioVex Inc | ||
Full Title: An Extension Protocol to Evaluate the Efficacy and Safety of Extended Use Treatment with OncoVEX GM-CSF or GM-CSF for Eligible Melanoma Patients Participating in Study 005/05 | ||
Medical condition: Unresectable Stage IIIb, IIIc and IV Melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012934-63 | Sponsor Protocol Number: D0102C00004 | Start Date*: 2009-10-23 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Randomised, Double-blind, Placebo-controlled, Multi-centre Study to Assess the Efficacy and Safety of AZD8931 In Combination with Anastrozole, Compared to Anastrozole alone, in Post-men... | |||||||||||||
Medical condition: Locally Advanced or Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005666-37 | Sponsor Protocol Number: ODX-003 | Start Date*: 2016-02-26 | |||||||||||
Sponsor Name:DexTech Medical AB | |||||||||||||
Full Title: A randomized, double-blind, dose finding, repeat dose Phase II multicentre study of ODX for the treatment of patients with castration resistant prostate cancer (CRPC) and skeletal metastases | |||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer (CRPC) and skeletal metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) EE (Completed) LV (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000951-14 | Sponsor Protocol Number: RhoVac-002 | Start Date*: 2019-08-26 | |||||||||||
Sponsor Name:RhoVac ApS | |||||||||||||
Full Title: A Phase 2, Double-Blind, Placebo Controlled Study of RV001V in Men with Biochemical Failure following Curatively Intended Therapy for Localized Prostate Cancer | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) FI (Completed) SE (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2011-004501-24 | Sponsor Protocol Number: CT-2011-01 | Start Date*: 2012-03-06 | |||||||||||
Sponsor Name:CureTech Ltd. | |||||||||||||
Full Title: Phase II study to evaluate the safety, tolerability and efficacy of CT-011 administered intravenously to patients with metastatic melanoma | |||||||||||||
Medical condition: Metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000232-34 | Sponsor Protocol Number: NASIR-HCC | Start Date*: 2017-09-11 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: A multicenter, open-label, single-arm study of the safety and antitumoral efficacy of nivolumab in combination with selective internal radiation therapy (SIRT) using SIR-Spheres for the treatment o... | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005251-25 | Sponsor Protocol Number: CABACARE | Start Date*: 2017-04-07 | ||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||
Full Title: CABAzitaxel with or without prednisone in patients with metastatic CAstration REsistant prostate cancer (mCRPC) progressed during or after a previous docetaxel-based chemotherapy: a multi-center, p... | ||||||||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer (mCRPC) progressed during or after a previous docetaxel-based chemotherapy. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003836-22 | Sponsor Protocol Number: 114-NH-301 | Start Date*: 2007-03-15 | |||||||||||
Sponsor Name:Biogen Idec Ltd. | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind Study of Galiximab in Combination with Rituximab Compared with Rituximab in Combination with Placebo for the Treatment of Subjects with Relapsed or Refractory,... | |||||||||||||
Medical condition: Relapsed or Refractory, Follicular Non-Hodgkin’s Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) CZ (Prematurely Ended) AT (Prematurely Ended) LT (Prematurely Ended) GB (Completed) SE (Prematurely Ended) IT (Prematurely Ended) ES (Completed) LV (Prematurely Ended) DE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021946-22 | Sponsor Protocol Number: DeCOG–MM-PAL11 | Start Date*: 2011-04-05 | |||||||||||||||||||||
Sponsor Name:University Hospital Essen | |||||||||||||||||||||||
Full Title: THE IPI – MULTIBASKET TRIAL IN ADVANCED OCULAR MELANOMA: PROSPECTIVE CLINICAL PHASE II MULTIBASKET STUDY IN OCULAR MELANOMA PATIENTS WITH ADVANCED DISEASE | |||||||||||||||||||||||
Medical condition: Histologically proven uveal melanoma Measurable disease according to RECIST in unresectable stage III-IV | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000618-23 | Sponsor Protocol Number: ORN-01 | Start Date*: 2015-05-05 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen/NÄL | ||||||||||||||||||
Full Title: Treatment of osteoradionecrosis (ORN) with pentoxifylline and α-tocopherol (PENTO) | ||||||||||||||||||
Medical condition: Osteoradionecrosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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