- Trials with a EudraCT protocol (44,344)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,344 result(s) found.
Displaying page 1,879 of 2,218.
EudraCT Number: 2020-004851-34 | Sponsor Protocol Number: BT008E | Start Date*: 2021-04-14 | |||||||||||
Sponsor Name:INSIGHTEC | |||||||||||||
Full Title: Assessment of Safety and Feasibility of Exablate Blood-Brain Barrier Disruption for the Treatment of High-Grade Glioma in Patients Undergoing Standard Chemotherapy | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002672-13 | Sponsor Protocol Number: CRHACS | Start Date*: 2021-03-18 | |||||||||||
Sponsor Name:ALMA MATER STUDIORUM UNIVERSITà DI BOLOGNA | |||||||||||||
Full Title: CPAP Reduces Hypoxemia After Cardiac Surgery (CRHACS Trial). A randomized controlled trial | |||||||||||||
Medical condition: Hypoxemia after cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003127-41 | Sponsor Protocol Number: BT009E | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:INSIGHTEC | |||||||||||||
Full Title: Assessment of Safety and Feasibility of Exablate Blood-Brain Barrier Disruption (BBBD) with Microbubble Resonators for the Treatment of Recurrent Glioblastoma (rGBM) in Subjects Undergoing Carbopla... | |||||||||||||
Medical condition: Recurrent Glioblastoma (rGBM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001503-20 | Sponsor Protocol Number: MedOPP150(ATRACTIB) | Start Date*: 2021-07-30 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
Full Title: PHASE II CLINICAL TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF FIRST LINE ATEZOLIZUMAB IN COMBINATION WITH PACLITAXEL AND BEVACIZUMAB (AVASTIN®) IN PATIENTS WITH ADVANCED OR METASTATIC TRIPLE-NEGAT... | |||||||||||||
Medical condition: Advanced or metastatic triple-negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005626-29 | Sponsor Protocol Number: IRFMN-SARCO-7953 | Start Date*: 2021-05-05 | ||||||||||||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||||||||||||
Full Title: A phase II study on trabectedin in combination with PPARg agonist pioglitazone in patients with round cell myxoid liposarcomas or dedifferentiated G1 and G2 liposarcomas with stable disease after a... | ||||||||||||||||||||||||||||
Medical condition: Patients with myxoid/round cell liposarcoma treated with at least 4 cycle of T alone with a stable disease at the last tumor evaluation | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001906-41 | Sponsor Protocol Number: MRHT_ES-IF_RCT001 | Start Date*: 2016-08-08 | |||||||||||
Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||
Full Title: A randomised control trial of intra articular injectates in knee osteoarthritis: A comparison of corticosteroid (Methylprednisolone Acetate) and NSAID (Ketorolac tromethamine) injections | |||||||||||||
Medical condition: Knee osteoarthritis is the condition of interest. Osteoarthritis is a common musculoskeletal complaint, with an underlying pathogenesis related to bio-mechanical stress loading, resulting in initia... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002076-13 | Sponsor Protocol Number: NS-065/NCNP-01-301 | Start Date*: 2020-03-02 | |||||||||||
Sponsor Name:NS Pharma, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Placebo-controlled, Multi-center Study to Assess the Efficacy and Safety of Viltolarsen in Ambulant Boys with Duchenne Muscular Dystrophy (DMD) | |||||||||||||
Medical condition: Duchenne Muscular Dystrophy (DMD) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) ES (Ongoing) NL (Ongoing) GR (Completed) IT (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001500-38 | Sponsor Protocol Number: LIN-MD-64-EU-3 | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Safety and Efficacy Study of Linaclotide Administered Orally to Children, Ages 6 to 17 Years, With Functional C... | |||||||||||||
Medical condition: Functional Constipation | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) EE (Completed) DE (Completed) PL (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000540-60 | Sponsor Protocol Number: SGNTUC-017 | Start Date*: 2020-08-10 | ||||||||||||||||
Sponsor Name:Seattle Genetics, Inc. | ||||||||||||||||||
Full Title: MOUNTAINEER: A Phase 2, Open Label Study of Tucatinib Combined with Trastuzumab in Patients with HER2+ Metastatic Colorectal Cancer | ||||||||||||||||||
Medical condition: HER2+ Metastatic Colorectal Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002633-34 | Sponsor Protocol Number: ESK-001-006 | Start Date*: 2023-02-07 | |||||||||||
Sponsor Name:Alumis Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ESK-001 in Patients with Moderate to Severe Plaque Psoriasis | |||||||||||||
Medical condition: Moderate to Severe Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001517-16 | Sponsor Protocol Number: PQGrass306 | Start Date*: 2022-09-29 | |||||||||||
Sponsor Name:Allergy Therapeutics (UK) Ltd. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of PQ Grass in subjects with seasonal allergic rhinitis and/or rhinoconjunctivitis induced by grass... | |||||||||||||
Medical condition: Seasonal allergic rhinitis and/or rhinoconjunctivitis induced by grass pollen exposure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) AT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003415-19 | Sponsor Protocol Number: JM-010CS03 | Start Date*: 2018-10-31 |
Sponsor Name:Contera Pharma | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study in Parkinson’s Disease Patients With Moderate to Severe Dyskinesia to Assess the Efficacy and Safety/Tolerability of Two Dose Co... | ||
Medical condition: Parkinson’s Disease Patients With Moderate to Severe Dyskinesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Restarted) IT (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000176-11 | Sponsor Protocol Number: HM-GLP2-201 | Start Date*: 2021-12-20 | |||||||||||
Sponsor Name:Hanmi Pharmaceutical Co., Ltd. | |||||||||||||
Full Title: A Multicenter, Proof-of-concept, Phase 2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HM15912 in Adult Subjects with Short Bowel Syndrome-associated Intesti... | |||||||||||||
Medical condition: Short Bowel Syndrome-associated Intestinal Failure (SBS-IF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001144-39 | Sponsor Protocol Number: GBMBIBT01 | Start Date*: 2008-08-12 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: A randomized phase II trial with bevacizumab, irinotecan and cerebral radiotherapy versus bevacizumab, temozolomide and cerebral radiotherapy as first line treatment for patients with glioblastoma ... | |||||||||||||
Medical condition: This study investigates first line experimental non-surgical therapy in patients with glioblastoma multiforme in good performance status | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004399-16 | Sponsor Protocol Number: CHERUB01 | Start Date*: 2021-04-28 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Efficacy of erenumab in chronic cluster headache: A 10-week double-blind, randomized, placebo-controlled, multicentric trial | |||||||||||||
Medical condition: chronic cluster headache | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021407-24 | Sponsor Protocol Number: BIBF1120-GBM | Start Date*: 2010-11-09 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Phase II study of BIBF 1120 in recurrent Glioblastoma multiforme | |||||||||||||
Medical condition: Relapsed glioblastoma multiforme | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003925-13 | Sponsor Protocol Number: CA209-9UP | Start Date*: 2018-02-19 |
Sponsor Name:Rigshospitalet | ||
Full Title: A phase II Open Label, two-armed Translational Study of Nivolumab in Combination with Bevacizumab for Recurrent Glioblastoma | ||
Medical condition: Glioblastoma, recurrent/progressive | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006011-74 | Sponsor Protocol Number: BI-Brain-01 | Start Date*: 2007-02-01 |
Sponsor Name:Rigshospitalet | ||
Full Title: A phase II trial with bevacizumab and irinotecan for patients with primary brain tumors and progression after standard therapy | ||
Medical condition: Primary malignant brain tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001308-35 | Sponsor Protocol Number: EB-UGI 01 | Start Date*: 2006-05-04 |
Sponsor Name:The Finsen Center, Rigshospitalet | ||
Full Title: A phase II study of erlotinib and bevacizumab in patients with advanced upper gastrointestinal carcinomas, refractory or intolerable to standard systemic therapy | ||
Medical condition: Histologically or cytologically verified upper gastro-intestinal carcinoma, including carcinomas of the esophagus, cardia, stomac, pancreas, gall bladder, and bile ducts of the following histologic... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001049-42 | Sponsor Protocol Number: | Start Date*: 2012-07-05 |
Sponsor Name:Department of Oncology, Rigshospitalet | ||
Full Title: MRI-perfusion and FLT- and FET-PET during bevacizumab monotherapy for patients with recurrent Glioblastoma Multiforme | ||
Medical condition: Recurrent Glioblastoma multiforme | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
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