- Trials with a EudraCT protocol (44,396)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,396 result(s) found.
Displaying page 1,882 of 2,220.
| EudraCT Number: 2017-004239-35 | Sponsor Protocol Number: 2017/16 | Start Date*: 2019-09-26 | |||||||||||
| Sponsor Name:Centre Antoine Lacassagne | |||||||||||||
| Full Title: Randomized Phase II, 2-arm Study of Immunomodulation with Atezolizumab concomitant with High Dose Radiation (SBRT) Versus SBRT Alone in Patients with Oligometastatic Sarcomas | |||||||||||||
| Medical condition: Soft tissue sarcoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005600-19 | Sponsor Protocol Number: APHP200072 | Start Date*: 2022-06-17 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
| Full Title: LEvOsimendaN vs. Placebo Before Tricuspid VAlve Surgery in Patients with Right Ventricular Dysfunction | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-020912-12 | Sponsor Protocol Number: VP-VEC-162-3202 | Start Date*: 2010-08-26 | |||||||||||
| Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
| Full Title: Open-label safety study of a 1-year 20 mg dose regimen of tasimelteon for the treatment of Non-24-Hour Sleep-Wake Disorder (N24HSWD) in blind individuals with no light perception. | |||||||||||||
| Medical condition: Non-24 Hour Sleep-Wake Disorder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004402-10 | Sponsor Protocol Number: APHP180587 | Start Date*: 2020-03-11 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Fecal transplantation to Eradicate Colonizing Emergent Superbugs | |||||||||||||
| Medical condition: Patients colonized with MDR-GNB (multi-drug resistant Gram Negative bacteria ) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000297-17 | Sponsor Protocol Number: 69HCL19_0153 | Start Date*: 2021-01-21 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: IMMUNOGAST: An umbrella phase 2 trial to assess personalized targeted IMMUNOtherapy-based regimens in recurrent advanced/metastatic GASTric adenocarcinoma patients | |||||||||||||
| Medical condition: For patients with advanced/metastatic gastric adenocarcinomas in progression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000637-12 | Sponsor Protocol Number: P170909J | Start Date*: 2019-03-29 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Efficacy and safety of rituximab in the treatment of good prognosis microscopic polyangiitis | |||||||||||||
| Medical condition: Patients with newly diagnosed or relapsing MPA, without any poor prognosis marker (FFS=0). Stratification will be made according to peripheral nerve involvement. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002403-34 | Sponsor Protocol Number: 009175QM | Start Date*: 2014-04-15 |
| Sponsor Name:Queen Mary, University of London | ||
| Full Title: A Randomized Phase II Study of Fulvestrant in Combination with the dual mTOR Inhibitor AZD2014 or Everolimus or Fulvestrant alone in Estrogen Receptor-Positive Advanced or Metastatic Breast Cancer. | ||
| Medical condition: Estrogen receptor-positive advanced or metastatic breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DE (Prematurely Ended) PT (Prematurely Ended) ES (Completed) HU (Completed) FR (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-001854-74 | Sponsor Protocol Number: RBHP-2021-ELJEZI | Start Date*: 2021-07-28 | ||||||||||||||||
| Sponsor Name:CHU de Clermont-Ferrand | ||||||||||||||||||
| Full Title: - | ||||||||||||||||||
| Medical condition: - | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004319-29 | Sponsor Protocol Number: P170914J | Start Date*: 2021-10-04 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: " LEVOSIMENDAN to facilitate weaning from ECMO in severe cardiogenic shock patients | |||||||||||||
| Medical condition: Adult patients with acute cardiogenic shock refractory to conventional therapy placed on VA-ECMO support and for whom withdrawal from ECMO is possible. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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) | |||||||||||||
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