- Trials with a EudraCT protocol (44,346)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,346 result(s) found.
Displaying page 2,118 of 2,218.
EudraCT Number: 2011-004418-40 | Sponsor Protocol Number: H9H-MC-JBAL | Start Date*: 2012-02-23 | |||||||||||
Sponsor Name:Lilly S.A, | |||||||||||||
Full Title: A Phase 2 Study of LY2157299 Monohydrate Monotherapy or LY2157299 Monohydrate plus Lomustine Therapy compared to Lomustine Monotherapy in Patients with Recurrent Glioblastoma | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000692-24 | Sponsor Protocol Number: EVARBD | Start Date*: 2017-04-05 | |||||||||||
Sponsor Name:AZIENDA USL TOSCANA SUD EST Sezione di Arezzo | |||||||||||||
Full Title: "Evaluation of efficacy and accuracy of a CTA low dose protocol for Pazients with EVAR" | |||||||||||||
Medical condition: Patients with aortic aneurism who underwent to endovascular repair of aortic aneurism. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000151-40 | Sponsor Protocol Number: SGM-CLIN03 | Start Date*: 2019-06-13 | ||||||||||||||||||||||||||
Sponsor Name:Surgimab | ||||||||||||||||||||||||||||
Full Title: Multicenter, semi-blinded, randomized, controlled, parallel arms clinical study on the performance of SGM-101, a fluorochrome-labeled anti-carcino-embryonic antigen (CEA) monoclonal antibody, for t... | ||||||||||||||||||||||||||||
Medical condition: Patients undergoing curative surgery for colorectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) NL (Ongoing) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003367-19 | Sponsor Protocol Number: NUC-5/PSC | Start Date*: 2017-09-28 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase III study comparing norursodeoxycholic acid capsules with placebo in the treatment of primary sclerosing cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) is a slowly progressing chronic cholestatic liver disease of assumed autoimmune, but finally unidentified etiology, characterized by a chronic inflammatory and ... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) HU (Trial now transitioned) LT (Completed) FI (Trial now transitioned) CZ (Prematurely Ended) BE (Completed) DK (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) SE (Completed) NO (Trial now transitioned) PL (Trial now transitioned) IE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002190-21 | Sponsor Protocol Number: MAR-BAS-18-005 | Start Date*: 2020-07-08 | |||||||||||||||||||||
Sponsor Name:Fondazione per la Medicina Personalizzata | |||||||||||||||||||||||
Full Title: The ROME trial from histology to target: the road to personalize target therapy and immunotherapy | |||||||||||||||||||||||
Medical condition: Patients with progressive disease (recurrent and/or metastatic) of breast cancer, metastatic gastro-intestinal tumors, non small cell lung cancer (NSCLC) or others. Patients should have completed a... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013294-18 | Sponsor Protocol Number: 2009-06-01 | Start Date*: 2010-08-02 |
Sponsor Name:Universitätsklinikum Greifswald der Ernst-Moritz-Arndt Universität Greifswald AöR | ||
Full Title: Magnesiumsulfate in the prevention of post-ERCP pancreatitis – a prospective randomized, placebo-controlled multicenter study | ||
Medical condition: Post-ERCP pancreatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001465-24 | Sponsor Protocol Number: GC-LTFU-001 | Start Date*: 2018-02-26 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: Long-Term Follow-up Protocol for Subjects Treated with Gene-Modified T cells. | |||||||||||||
Medical condition: Defined by parent protocol. The study will enroll all adult and paediatric subjects who received at least one genetically modified T cells infusion in a previous Celgene sponsored study. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) GB (GB - no longer in EU/EEA) NO (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003829-15 | Sponsor Protocol Number: AID-ICU | Start Date*: 2017-11-30 |
Sponsor Name:Zealand University Hospital | ||
Full Title: Agents Intervening against Delirium in the Intensive Care Unit (AID-ICU) | ||
Medical condition: Treatment of delirium in critically ill adult patients in intensive care unit. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) FI (Completed) ES (Ongoing) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003225-15 | Sponsor Protocol Number: HALO-ICU | Start Date*: 2017-12-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Comparison between inhaled sedation with Sevoflurane vs endovenous sedation with Propofol in the Intensive Care Unit: a randomized prospective trial | |||||||||||||
Medical condition: Preoperative-scheduled sedation in surgical patients admitted in the Intensive Care Unit (ICU) for postoperative monitoring | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003022-89 | Sponsor Protocol Number: 1.1 | Start Date*: 2019-10-18 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: GUT-DERIVED INCRETIN HORMONES IN THE PATHOPHYSIOLOGY OF TYPE 1 DIABETES MELLITUS; EFFECT OF METFORMIN TREATMENT (THE INCREDIBLE-ME TRIAL) | |||||||||||||
Medical condition: GUT-DERIVED INCRETIN HORMONES IN THE PATHOPHYSIOLOGY OF TYPE 1 DIABETES MELLITUS; EFFECT OF METFORMIN TREATMENT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004295-55 | Sponsor Protocol Number: RPC01-3204 | Start Date*: 2018-03-08 | |||||||||||
Sponsor Name:Celgene International II Sàrl | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-Label Extension Study of Oral Ozanimod for Moderately to Severely Active Crohn’s Disease | |||||||||||||
Medical condition: Moderately to Severely Active Crohn’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) SK (Trial now transitioned) LV (Trial now transitioned) LT (Completed) CZ (Trial now transitioned) FR (Trial now transitioned) SI (Completed) AT (Completed) BG (Trial now transitioned) DE (Trial now transitioned) GR (Completed) ES (Ongoing) SE (Prematurely Ended) NL (Ongoing) PL (Trial now transitioned) BE (Completed) IE (Trial now transitioned) GB (Not Authorised) DK (Completed) PT (Trial now transitioned) HR (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001008-13 | Sponsor Protocol Number: SUPERIOR | Start Date*: 2018-07-09 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: A SUPAR GUIDED DOUBLE BLIND RANDOMIZED CLINICAL TRIAL OF INITIATION OF ANTIBIOTICS FOR PRESUMED INFECTION AT THE EMERGENCY DEPARTMENT: THE SUPERIOR TRIAL | |||||||||||||
Medical condition: Α suPAR guided early antibiotic administration at the Emergency Room for presumed infection and sepsis and evaluation of the impact of this intervention to the patients’ final outcome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000404-42 | Sponsor Protocol Number: RH-ITA-007 | Start Date*: 2018-03-20 | |||||||||||
Sponsor Name:Dept. of Intensive Care, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: The Conservative vs. Liberal Approach to fluid therapy of Septic Shock in Intensive Care Trial | |||||||||||||
Medical condition: Septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) CZ (Completed) ES (Prematurely Ended) BE (Completed) FI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000572-15 | Sponsor Protocol Number: GRASPANC-2018-01 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:ERYTECH Pharma | |||||||||||||
Full Title: A Randomized, Phase 3 Study of Eryaspase in Combination with Chemotherapy versus Chemotherapy Alone as Second-Line Treatment in Patients with Pancreatic Adenocarcinoma | |||||||||||||
Medical condition: Pancreatic Adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) ES (Completed) AT (Completed) DE (Completed) NL (Completed) DK (Prematurely Ended) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003350-25 | Sponsor Protocol Number: SPON1751-19 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: An open label, 3-arm, Randomised phase II study to Compare the Safety and Efficacy of Ponatinib in combination with either Chemotherapy or Blinatumomab with Imatinib plus Chemotherapy as front-line... | |||||||||||||
Medical condition: Philadelphia chromosome positive (Ph+ or BCR-ABL+) Acute Lymphoblastic Leukaemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SE (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004892-11 | Sponsor Protocol Number: SteP-on | Start Date*: 2021-04-22 | |||||||||||
Sponsor Name:OSPEDALE SANTA MARIA DELLA MISERICORDIA | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicentre study to evaluate the effect of safinamide on freezing of gait (FOG) in mid- to late-stage fluctuating PD patients | |||||||||||||
Medical condition: • Subjects of both genders over 18 years of age, with a clinical diagnosis of idiopathic PD • A Modified Hoehn and Yahr stage of = 4 in the “off” state; • A stable (4 weeks since last modification)... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003726-93 | Sponsor Protocol Number: HALO-HCA2017 | Start Date*: 2019-07-31 | |||||||||||
Sponsor Name:HELLENIC INSTITUTE FOR THE STUDY OF SEPSIS | |||||||||||||
Full Title: Heparin Anticoagulation to improve Outcomes in septic shock : The HALO International phase II RCT. | |||||||||||||
Medical condition: HEPARIN Anticoagulation to improve outcomes in septic shock : the HALO International Phase II RCT | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001466-11 | Sponsor Protocol Number: SAVE | Start Date*: 2020-04-15 | |||||||||||
Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
Full Title: suPAR-GUIDED ANAKINRA TREATMENT FOR VALIDATION OF THE RISK AND EARLY MANAGEMENT OF SEVERE RESPIRATORY FAILURE BY COVID-19: THE SAVE OPEN-LABEL, NON-RANDOMIZED SINGLE-ARM TRIAL | |||||||||||||
Medical condition: Lower respiratory tract infection by Covid-19 at high risk for development of severe respiratory failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002538-14 | Sponsor Protocol Number: 218672 | Start Date*: 2023-06-12 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: 17-beta-Hydroxysteroid Dehydrogenase type 13 Minimization for the treatment of NASH (HORIZON): A Double-Blind, Placebo-Controlled Phase 2b Study to Evaluate the Efficacy and Safety of GSK4532990 in... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001987-31 | Sponsor Protocol Number: COMBAT_T2_NASH_002 | Start Date*: 2020-08-05 | |||||||||||
Sponsor Name:Deutsche Diabetes Forschungsgesellschaft e.V. | |||||||||||||
Full Title: COMBined Active Treatment in Type 2 Diabetes with NASH | |||||||||||||
Medical condition: Diabetes mellitus type 2 (T2D) and non-alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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