- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 1,889 of 2,219.
| EudraCT Number: 2016-000297-38 | Sponsor Protocol Number: CL1-68587-003 | Start Date*: 2016-06-22 | ||||||||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | ||||||||||||||||||
| Full Title: Long-term follow-up study of patients who have previously been exposed to UCART19 / ALLO-501 (allogeneic engineered T-cells expressing a lentiviral-based anti-CD19 chimeric antigen receptor) | ||||||||||||||||||
| Medical condition: Advanced lymphoid malignancies | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Ongoing) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004739-22 | Sponsor Protocol Number: DER-201805 | Start Date*: 2021-03-16 | ||||||||||||||||
| Sponsor Name:Rheinische Friedrich-Wilhelms-Universität Bonn | ||||||||||||||||||
| Full Title: Efficacy of ruxolitinib cream in Prurigo nodularis patients: A randomized, placebo-controlled pilot study (PRUX) | ||||||||||||||||||
| Medical condition: Patients with symptomatic Prurigo nodularis with active skin manifestations | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-001389-12 | Sponsor Protocol Number: PICS1.0 | Start Date*: 2020-10-29 | ||||||||||||||||
| Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
| Full Title: The Postoperative Iron in Cardiac Surgery (PICS-) trial: A randomised clinical trial comparing the efficacy of single-, high-dose intravenous iron and oral iron for the treatment of anaemia followi... | ||||||||||||||||||
| Medical condition: Anaemia following cardiac surgery | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-002489-15 | Sponsor Protocol Number: 380119 | Start Date*: 2021-03-23 | |||||||||||
| Sponsor Name:Medinova AG | |||||||||||||
| Full Title: Comparative study of the efficacy and safety of vaginally applied Dequalinium Chloride (10 mg) and orally applied Metronidazole (2 x 500 mg) in the treatment of bacterial vaginosis | |||||||||||||
| Medical condition: Bacterial vaginosis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001988-24 | Sponsor Protocol Number: M602011069 | Start Date*: 2021-09-07 | |||||||||||
| Sponsor Name:Merz Pharmaceuticals GmbH | |||||||||||||
| Full Title: Prospective, randomized, double-blind, placebo-controlled, parallel-group trial with an open-label period to investigate the efficacy and safety of NT201 in the unilateral and bilateral treatment o... | |||||||||||||
| Medical condition: Essential tremor [ET] of the upper limb [UL] | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000714-33 | Sponsor Protocol Number: PT26/17/01 | Start Date*: 2023-02-21 | |||||||||||
| Sponsor Name:tiakis Biotech AG (formerly Proteo Biotech AG) | |||||||||||||
| Full Title: Efficacy and safety of Tiprelestat for treatment of severe COVID-19 (COMCOVID trial) | |||||||||||||
| Medical condition: Adult patients with COVID-19 fulfilling the following criteria: -First laboratory-confirmation of the current episode of SARS-CoV-2 infection (COVID-19) as determined by PCR or antigen test (no sel... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001587-30 | Sponsor Protocol Number: 012657 | Start Date*: 2019-07-26 | ||||||||||||||||
| Sponsor Name:Queen Mary University London | ||||||||||||||||||
| Full Title: AZD1656 in Transplantation with Diabetes tO PromoTe Immune TOleraNce | ||||||||||||||||||
| Medical condition: renal transplant AND type 2 diabetes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2005-005874-65 | Sponsor Protocol Number: ISS-UZA-5/26/99 | Start Date*: 2006-01-13 |
| Sponsor Name:University Hospital Antwerp | ||
| Full Title: Non-invasive monitoring of airway inflammation in asthmatic patients during adaptation of inhaled steroid therapy | ||
| Medical condition: asthma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001983-31 | Sponsor Protocol Number: 1842012 | Start Date*: 2012-05-25 | |||||||||||
| Sponsor Name:Juha Hartikainen | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: Coronary artery by-pass surgery patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000458-72 | Sponsor Protocol Number: 260411 | Start Date*: 2012-05-25 | |||||||||||
| Sponsor Name:Juha Hartikainen | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: Coronary artery by-pass surgery patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001528-16 | Sponsor Protocol Number: INS1009-202 | Start Date*: 2022-05-30 | |||||||||||
| Sponsor Name:Insmed Incorporated | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to valuate the Efficacy, Safety, and Pharmacokinetics of Treprostinil Palmitil Inhalation Powder in participants with Pu... | |||||||||||||
| Medical condition: Participants with Pulmonary Arterial Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) IT (Trial now transitioned) AT (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002221-35 | Sponsor Protocol Number: P2013/PE1 | Start Date*: 2014-12-18 | ||||||||||||||||
| Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola | ||||||||||||||||||
| Full Title: Prospective Randomized Study Comparing the Efficacy and Safety of Pleural Drainage by Video-Assisted Thoracoscopic With Pleural Drain Associated With Urokinase in the Treatment of Parapneumonic Ple... | ||||||||||||||||||
| Medical condition: Parapneumonic pleural effusion | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-004564-55 | Sponsor Protocol Number: COSTAL-2013 | Start Date*: 2014-03-10 | |||||||||||
| Sponsor Name:MEDITOP Gyógyszeripari Kft | |||||||||||||
| Full Title: A randomized, multicenter, double-blind, placebo controlled, parallel study to assess the efficacy and safety of the combined administration of sertraline and lamotrigine in subjects with chronic l... | |||||||||||||
| Medical condition: Chronic low back pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) RO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001427-38 | Sponsor Protocol Number: P/2017/337 | Start Date*: 2018-07-04 |
| Sponsor Name:CHU Besançon | ||
| Full Title: Activité et tolérance d’une immunothérapie par avelumab en maintenance après une première ligne de polychimiothérapie contenant un sel de platine chez les patients atteints de carcinome épidermoïde... | ||
| Medical condition: carcinome épidermoïde de verge | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002390-28 | Sponsor Protocol Number: INSPIRE | Start Date*: 2022-10-10 | ||||||||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | ||||||||||||||||||
| Full Title: IMMUNOTHERAPY NAVIGATED BY SERUM PRESEPSIN FOR INFECTIONS OF THE RESPIRATORY TRACT: THE INSPIRE DOUBLE-BLIND, RANDOMIZED, PHASE IIa EXPLORATORY TRIAL | ||||||||||||||||||
| Medical condition: community-acquired pneumonia, hospital-acquired pneumonia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-000642-16 | Sponsor Protocol Number: H4COVID | Start Date*: 2022-03-04 | |||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
| Full Title: Hydrogen sulfate guided therapy with STS for COVID-19 patients in need of critical care: The H4COVID open-label, randomized, triple-arm trial | |||||||||||||
| Medical condition: Assessment of clinical improvement of critically ill patients with confirmed Covid-19 by administering of sodium thiosulfate | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001302-15 | Sponsor Protocol Number: BIO-CT-001 | Start Date*: 2019-09-13 | |||||||||||
| Sponsor Name:BIOKOSMOS S.A. | |||||||||||||
| Full Title: Phase III study of Positron/Computerized Tomography (PETCT) with F-18-PSMA-1007 versus F-18-Fluorocholine to compare the detection rate of prostate cancer lesions in patients with biochemical recur... | |||||||||||||
| Medical condition: Prostate cancer recurrent | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-003611-62 | Sponsor Protocol Number: LIB003-003 | Start Date*: 2020-03-20 | |||||||||||
| Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
| Full Title: Randomized, Open-Label, Cross-Over, Phase 3 Study to Evaluate the Efficacy and Safety of LIB003 with Evolocumab in Homozygous Familial Hypercholesterolemia Patients on Stable Lipid-Lowering Therapy. | |||||||||||||
| Medical condition: Homozygous Familial Hypercholesterolemia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005989-38 | Sponsor Protocol Number: | Start Date*: 2012-11-01 |
| Sponsor Name:Norwegian University of Science and Technology | ||
| Full Title: A SAFETY AND EFFICACY STUDY OF ADDING LOW DOSE PEGYLATED IFN-ΑLPHA 2B TO STANDARD DOSE DASATINIB IN PATIENTS WITH NEWLY DIAGNOSED CHRONIC PHASE CHRONIC MYELOID LEUKEMIA | ||
| Medical condition: Chronic myeloid leukemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) FI (Completed) SE (Ongoing) DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001264-38 | Sponsor Protocol Number: MOU-2017-01 | Start Date*: 2017-10-16 |
| Sponsor Name:Masaryk Memorial Cancer Institute | ||
| Full Title: Sequential FDG-PET and Plasma/Tissue miRNA as a Biomarkers of Preoperative Treatment Strategy in Locally Advanced Oesophago-Gastric Cancer | ||
| Medical condition: locally advanced resectable oesophago-gastric adenocarcinoma (Siewert I – III) with T3N0, T4N0, T2 – T4N+, stage Ib – IIIc | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) SK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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