- Trials with a EudraCT protocol (38,623)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1,012)
38,623 result(s) found for: 2-.
Displaying page 339 of 1,932.
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) |
EudraCT Number: 2020-005544-34 | Sponsor Protocol Number: CARVIN | Start Date*: 2021-02-04 | |||||||||||
Sponsor Name:URSAPHARM Arzneimittel GmbH | |||||||||||||
Full Title: Double-blind placebo-controlled proof-of-concept trial to demonstrate the anti-viral efficacy of different doses of azelastine in COVID-19 positive patients. | |||||||||||||
Medical condition: Diagnosis of SARS-CoV-2 infection documented by a positive PCR test (patients do not need to suffer from COVID-19 symptoms) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000142-20 | Sponsor Protocol Number: 2003056 | Start Date*: 2004-10-01 | |||||||||||
Sponsor Name:Procter & Gamble Pharmaceuticals | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Parallel-group, Placebo-Controlled Study of Pexelizumab in Patients with Acute Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention | |||||||||||||
Medical condition: Following as ST-wave elevation myocardial infarction, there is local ischemia. When reperfusion occurs, there is a complement mediated inflammatory reponse, known as reperfusion injury, and a syst... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003260-53 | Sponsor Protocol Number: 102010 | Start Date*: 2006-07-24 | |||||||||||
Sponsor Name:Danmarks Farmaceutiske Universitet | |||||||||||||
Full Title: Lokal administration af morfin: Evaluering af den smertestillende effekt på stomatitis hos børn. | |||||||||||||
Medical condition: Stomatitis som bivirkning til kemoterapi. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005521-23 | Sponsor Protocol Number: QUAMED13 | Start Date*: 2014-06-19 | ||||||||||||||||
Sponsor Name:QUALIPHAR NV | ||||||||||||||||||
Full Title: Efficacy and safety assessment of Chlorhexidine hydrochloride - Lidocaine hydrochloride (MEDICA ®) versus placebo in adult patients with sore throat and/or acute pharyngitis | ||||||||||||||||||
Medical condition: Sore throat or acute pharyngitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001802-32 | Sponsor Protocol Number: C1501 | Start Date*: 2015-08-14 | |||||||||||
Sponsor Name:Biologische Heilmittel Heel GmbH | |||||||||||||
Full Title: Neuronal correlates of Neurexan® action in mildly to moderately stressed probands - a randomized, placebo-controlled, double-blind, cross-over trial of mode of action and response prediction by fun... | |||||||||||||
Medical condition: mildly to moderately stressed probands | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002598-49 | Sponsor Protocol Number: CRO1885 | Start Date*: 2012-04-23 |
Sponsor Name:Imperial College Joint Research Office | ||
Full Title: The AXitinib MicroBubble UltraSound in metastatic Colorectal cancer trial | ||
Medical condition: Third line colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004676-35 | Sponsor Protocol Number: RVT-1401-2001 | Start Date*: 2019-10-23 | |||||||||||
Sponsor Name:Immunovant Sciences GmbH | |||||||||||||
Full Title: ASCEND GO2: A Phase 2b, Multicenter, Randomized, Double-blind, Placebo-controlled Study of RVT-1401 for the Treatment of Patients with Active, Moderate to Severe Graves’ Ophthalmopathy | |||||||||||||
Medical condition: Graves´Ophthalmopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005594-35 | Sponsor Protocol Number: TJB0603 | Start Date*: 2009-10-28 | |||||||||||
Sponsor Name:CHU Sart-Tilman | |||||||||||||
Full Title: Randomized double-blind study of mesenchymal stem cells (MSC) in patients undergoing matched unrelated allogeneic bone marrow or peripheral blood stem cell transplantation- A European multicentre s... | |||||||||||||
Medical condition: Hematological disorders of the following types: ALL: acute lymphoblastic leukemia in complete remission (<5% blasts in marrow) up to and including third remission (excluding relapse). AML: acute my... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000624-37 | Sponsor Protocol Number: CLOBOF3-17IA03 | Start Date*: 2022-10-05 | ||||||||||||||||
Sponsor Name:Laboratorios Salvat, S.A. | ||||||||||||||||||
Full Title: A Phase 3, multicenter, randomized, evaluator-blinded clinical trial to assess the safety and efficacy of Clobetasol propionate ophthalmic nanoemulsion, 0.05% compared to Prednisolone acetate, 1% i... | ||||||||||||||||||
Medical condition: Inflammation and pain associated with ocular surgery. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005330-14 | Sponsor Protocol Number: VAC31518COV2004 | Start Date*: 2021-04-06 | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | |||||||||||||
Full Title: An Open-label, Phase 2 Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Ad26.COV2.S in Healthy Pregnant Participants. | |||||||||||||
Medical condition: Healthy Pregnant Volunteers (Prevention of SARS-CoV-2-mediated COVID-19) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001201-93 | Sponsor Protocol Number: CABOPRE | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:Fundación ONCOSUR | |||||||||||||
Full Title: Phase II study for the evaluation of neoadjuvant treatment with cabozantinib prior to cytoreductive nephrectomy in patients with locally advanced or metastatic renal cell carcinoma | |||||||||||||
Medical condition: Locally Advanced or Metastatic Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003802-14 | Sponsor Protocol Number: CRC-PSO-SKINPEN-A-27 | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Skin penetration of anti-inflammatory compounds in lesional compared to non-lesional skin of psoriasis patients | |||||||||||||
Medical condition: Psoriasis vulgaris | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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