- Trials with a EudraCT protocol (38,656)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38,656 result(s) found for: 2-.
Displaying page 339 of 1,933.
| EudraCT Number: 2014-004655-31 | Sponsor Protocol Number: 1143-SCCHN-202 | Start Date*: 2015-03-25 | |||||||||||
| Sponsor Name:Debiopharm International S.A. | |||||||||||||
| Full Title: Preoperative window-of-opportunity (WoO) study of Debio 1143 with or without cisplatin (CDDP) in patients with resectable squamous cell carcinoma of the head and neck. | |||||||||||||
| Medical condition: Squamous cell carcinoma of the head and neck | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003599-39 | Sponsor Protocol Number: AMD3100-3102-DE | Start Date*: 2005-12-02 | |||||||||||
| Sponsor Name:AnorMED Corp. | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, comparative trial of AMD3100 (240 mcg/kg) plus G-CSF (10 mcg/kg) versus G-CSF (10 mcg/kg) plus placebo to mobilize and collect greater than or equal ... | |||||||||||||
| Medical condition: Mobilization of stem cells prior to autologous stem cell transplantation in patients with multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001414-25 | Sponsor Protocol Number: 205.417 | Start Date*: 2008-08-20 | |||||||||||
| Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
| Full Title: A Phase III randomised, double-blind, placebo-controlled, parallel-group trial to evaluate efficacy and safety of tiotropium inhalation solution delivered via Respimat ® inhaler (5 μg/day) over 48 ... | |||||||||||||
| Medical condition: Patients with severe persistent asthma who are still symptomatic despite being treated with high-dose inhaled corticosteroids and long-acting beta2-agonists. Additional asthma treatments are allowe... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003932-11 | Sponsor Protocol Number: I1F-MC-RHBV | Start Date*: 2016-04-19 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Active and Placebo-Controlled 16 Week Study Followed by Long Term Evaluation of Efficacy and Safety of Ixekizumab (LY2439821) in bDMARD-Naive Patients with ... | |||||||||||||
| Medical condition: Radiographic Axial Spondyloarthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) PL (Completed) NL (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003685-32 | Sponsor Protocol Number: PB-06-007 | Start Date*: 2012-01-27 | |||||||||||
| Sponsor Name:Protalix Biotherapeutics | |||||||||||||
| Full Title: A Multicenter Extension Study of Taliglucerase alfa in Adult Subjects with Gaucher Disease | |||||||||||||
| Medical condition: Gaucher disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003018-17 | Sponsor Protocol Number: SPD489-322 | Start Date*: 2012-10-10 |
| Sponsor Name:Shire Development LLC | ||
| Full Title: The SPD489-322 Phase 3, Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled, Flexible Dose Titration, Efficacy and Safety Study of SPD489 in Combination with an Antidepressant... | ||
| Medical condition: Major Depressive Disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005617-36 | Sponsor Protocol Number: TESEC-06 | Start Date*: 2012-05-30 | |||||||||||
| Sponsor Name:Statens Serum Institut | |||||||||||||
| Full Title: A phase III contact tracing trial comparing the diagnostic performance of C-Tb to QuantiFERON®-TB Gold In-Tube, in combination with a double blind randomized split body safety assessment of C-Tb ve... | |||||||||||||
| Medical condition: Tuberculosis diagnostic tool | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005556-25 | Sponsor Protocol Number: OFT-ETAMSILATO-4.2.2 | Start Date*: 2015-05-11 |
| Sponsor Name:Investigacion Independiente | ||
| Full Title: Open extension study for patients with age related macula degeneration who participated in the Fase IV-II clinical trial randomized, simulatedcontrolled treatment to evaluate safety and efficacy o... | ||
| Medical condition: Aged related macula degeneration (ARMD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-004210-26 | Sponsor Protocol Number: 14/0647 | Start Date*: 2016-11-22 | |||||||||||
| Sponsor Name:PRIMENT Clinical Trials Unit, UCL | |||||||||||||
| Full Title: A Phase IV double blind multi-site, individually randomised parallel group controlled trial investigating the use of citalopram, sertraline, fluoxetine and mirtazapine in preventing relapse in pati... | |||||||||||||
| Medical condition: Depression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001807-18 | Sponsor Protocol Number: TD-0903-0188 | Start Date*: 2020-05-18 | |||||||||||
| Sponsor Name:Theravance Biopharma Ireland Limited | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel-group, Multi-center Study of an Inhaled Pan-Janus Kinase Inhibitor, TD-0903, to Treat Symptomatic Acute Lung Injury Associated with... | |||||||||||||
| Medical condition: Acute lung injury associated with COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) RO (Completed) FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004022-15 | Sponsor Protocol Number: ANB019-003 | Start Date*: 2020-04-21 | |||||||||||
| Sponsor Name:AnaptysBio Inc | |||||||||||||
| Full Title: A Phase 2, Randomized, Placebo-controlled, Double-blind, Multiple Dose Study to Evaluate the Efficacy and Safety of ANB019 in Subjects with Palmoplantar Pustulosis | |||||||||||||
| Medical condition: Palmoplantar pustulosis (PPP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004255-70 | Sponsor Protocol Number: 205687 | Start Date*: 2017-05-29 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A randomised, double-blind, parallel group PhIII study to assess the clinical efficacy and safety of 100 mg SC Mepolizumab as an add on to maintenance treatment in adults with severe bilateral nasa... | |||||||||||||
| Medical condition: Treatment of nasal polyposis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) SE (Completed) NL (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014980-38 | Sponsor Protocol Number: TJB0909P1 | Start Date*: 2010-07-06 | |||||||||||
| Sponsor Name:CHU de Liège | |||||||||||||
| Full Title: Co-transplantation of mesenchymal stem cells and HLA-mismatched allogeneic hematopoietic cells after reduced-intensity conditioning: a phase II randomized double-blind study. | |||||||||||||
| Medical condition: Hematological malignancies confirmed histologically and not rapidly progressing: - AML in Complete Remission; - ALL in Complete Remission; - CML unresponsive/intolerant to Imatinib but not in b... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001305-41 | Sponsor Protocol Number: MicroVasc-DIVA | Start Date*: 2014-11-25 |
| Sponsor Name:GWT-TUD GmbH | ||
| Full Title: MICROVASCULAR AND ANTIINFLAMMATORY EFFECTS OF RIVAROXABAN COMPARED TO LOW DOSE ASPIRIN IN TYPE 2 DIABETIC PATIENTS WITH VERY HIGH CARDIOVASCULAR RISK AND SUBCLINICAL INFLAMMATION | ||
| Medical condition: Patients with type 2 diabetes and stable cardiovascular disease (CVD) and low grade inflammation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004483-38 | Sponsor Protocol Number: TMP001_MS | Start Date*: 2015-07-16 | |||||||||||
| Sponsor Name:Fraunhofer Gesellschaft for its Institute Fraunhofer Institute for Molecular Biology and Applied Ecology (IME) | |||||||||||||
| Full Title: TMP001 in relapsing-remitting multiple sclerosis: a multicentre open, baseline-controlled phase IIa clinical trial | |||||||||||||
| Medical condition: Patients with defined diagnosis of relapsing-remitting multiple sclerosis and at least 1 documented relapse during the previous year OR at least 2 documented relapses during the previous 2 years. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003672-12 | Sponsor Protocol Number: TM005 | Start Date*: 2019-01-29 | |||||||||||
| Sponsor Name:Saniona A/S | |||||||||||||
| Full Title: A 24-week phase 2, double-blind, randomized, placebo-controlled, single-centre safety and efficacy study to evaluate overall safety and tolerability of co-administration of tesofensine and metoprol... | |||||||||||||
| Medical condition: Hypothalmic injury-induced obesity (HIO) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001957-17 | Sponsor Protocol Number: DFNS02 | Start Date*: 2015-10-21 | |||||||||||
| Sponsor Name:Umeå University Hospital | |||||||||||||
| Full Title: THE EFFECT OF DIFLUNISAL ON FAMILIAL TRANSTHYRETIN AMYLOIDOSIS: An open label phase III extension study of the diflunisal trials (IND 68092 and DFNS01), and an open label observational study on p... | |||||||||||||
| Medical condition: Familial transthyretin amyloidosis complicated by cardiomyopathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000934-32 | Sponsor Protocol Number: AVXCLIN005 | Start Date*: 2021-10-25 | |||||||||||
| Sponsor Name:Coegin Pharma AB | |||||||||||||
| Full Title: A single-center, randomized double-blind, vehicle-controlled, dose-ranging decentralised clinical trial to evaluate the safety and efficacy of daily field-directed topical applications of AVX001 s... | |||||||||||||
| Medical condition: Actinic Keratosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002042-21 | Sponsor Protocol Number: PMT4979g | Start Date*: 2015-02-19 | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: AN OPEN-LABEL, PHASE I/II, DOSE-ESCALATION STUDY EVALUATING THE SAFETY AND TOLERABILITY OF GDC-0032 IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC SOLID TUMORS AND IN COMBINATION WITH ENDOCRINE TH... | |||||||||||||
| Medical condition: Patients with locally advanced or metastatic solid tumors and in combination with endocrine therapy in patients with locally advanced or metastatic hormone receptor-positive breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000346-18 | Sponsor Protocol Number: BST-SCI-02 | Start Date*: 2021-06-28 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: A phase I/II, randomized, double-blind, placebo-controlled, parallel, 2-arms clinical trial to assess the safety and efficacy of intrathecal administration of WJ-MSC in chronic traumatic cervical i... | |||||||||||||
| Medical condition: Cronic traumatic spinal cord injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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