- Trials with a EudraCT protocol (44,343)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,343 result(s) found.
Displaying page 1,527 of 2,218.
EudraCT Number: 2016-000489-50 | Sponsor Protocol Number: AC-009-IT | Start Date*: 2017-10-03 | |||||||||||
Sponsor Name:FONDAZIONE I.R.C.C.S. POLICLINICO SAN MATTEO | |||||||||||||
Full Title: A Phase II, Single Arm, Open Label, Efficacy and Safety Study of NEOD001 in Subjects with Light Chain (AL) Amyloidosis with Hepatic Involvement | |||||||||||||
Medical condition: AL amyloidosis with hepatic involvement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000700-32 | Sponsor Protocol Number: JDC02/07 | Start Date*: 2007-03-20 |
Sponsor Name:University hospitals Leuven | ||
Full Title: A randomised, double-blind, prospective study to compare the analgesic efficacy of 10 ml epidural loading dose levobupivacaine 0.5% versus levobupivacaine 0.25% in patients after major abdominal... | ||
Medical condition: patient controlled epidural pain therapy after major abdominal or thoracic surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-002084-85 | Sponsor Protocol Number: GBG26/TBP (UK sponsor ID-MO05/7222) | Start Date*: 2006-06-08 |
Sponsor Name:GBG Forschungs GmbH | ||
Full Title: A multicenter randomized phase III study to compare capecitabine alone or in combination with trastuzumab in patients with HER2 positive metastatic breast cancer and progression after previous trea... | ||
Medical condition: Patients with HER2 positive metastatic breast cancer and progression after previous treatment with trastuzumab. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) SI (Completed) DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000349-20 | Sponsor Protocol Number: IFG-01-0106 | Start Date*: 2006-10-11 |
Sponsor Name:Institut fuer Frauengesundheit GmbH | ||
Full Title: Prospective Randomized Phase-III-Trial of Paclitaxel plus Topotecan versus Topotecan plus Cisplatin in Recurrent or Persistent Cervical Carcinoma | ||
Medical condition: Chemotherapeutical treatment of patients with recurrent or persistent or metastatic cervical carcinoma stage IVb | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) AT (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003642-15 | Sponsor Protocol Number: Belimumab bei ITP | Start Date*: 2008-06-05 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: A Randomized, Double-blind Superiority Trial to Evaluate the Safety, Tolerability, and Efficacy of Belimumab in Refractory ITP Subjects | ||
Medical condition: Autoimmune thrombocytopenia (ITP) is a common disorder in which platelets are destroyed by autoantibodies. BAFF has been shown to be elevated in the serum of ITP patients. Blockage of BAFF has be... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-008361-35 | Sponsor Protocol Number: ISG/AIEOP EW-1 | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
Full Title: PHASE III TRIAL ON THE EFFICACY OF DOSE`S INTENSIFICATION IN PATIENTS WITH NON METASTATIC EWING`S SARCOMA | |||||||||||||
Medical condition: HOSPITAL PATIENTS AFFECTED BY EWING`S SARCOMA OR PNET WITH BONE`S INVOLVEMENT | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013274-41 | Sponsor Protocol Number: SPA-S-899/092 | Start Date*: 2010-05-10 | |||||||||||
Sponsor Name:SOCIETA` PRODOTTI ANTIBIOTICI | |||||||||||||
Full Title: Multicenter, randomized, parallel group open study to compare, in patients with postmenopausal osteoporosis, the effects of clodronate (Difosfonal) administered either intramuscularly at a dose of... | |||||||||||||
Medical condition: postmenopausal osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000891-13 | Sponsor Protocol Number: STW5-II/212-D-12-II-F;IMP17155 | Start Date*: 2014-07-21 |
Sponsor Name:Steigerwald Arzneimittelwerk GmbH | ||
Full Title: A randomised, double-blind, placebo-controlled multi-centre study to investigate the effectiveness and safety of STW5-II as add-on treatment for induction of remission in patients with mild to mode... | ||
Medical condition: Ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001862-56 | Sponsor Protocol Number: 64041575RSV2004 | Start Date*: 2018-01-09 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (... | |||||||||||||
Medical condition: Respiratory syncytial virus infection | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) BE (Prematurely Ended) FI (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) IE (Prematurely Ended) PT (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002253-38 | Sponsor Protocol Number: PHRC2015-06 | Start Date*: 2016-09-20 |
Sponsor Name:CHU Angers | ||
Full Title: Mesure de la clairance plasmatique du iohexol chez les patients sortant de réanimation après insuffisance rénale aiguë | ||
Medical condition: Insuffisance rénale non résolutive | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002732-70 | Sponsor Protocol Number: YV25718 | Start Date*: 2012-02-09 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A Phase IIIb Parallel Group, Open Label Study of Pegylated Interferon alfa-2a Monotherapy (PEG-IFN, Ro 25-8310) Compared to Untreated Control in Children with HBeAg Positive Chronic Hepatitis B in ... | |||||||||||||
Medical condition: Treatment of HBeAg positive chronic hepatitis B (CHB) in children. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) DE (Completed) PL (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014992-31 | Sponsor Protocol Number: AC-065A303 | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: Long-term single-arm open-label study, to assess the safety and tolerability of selexipag in patients with pulmonary arterial hypertension | |||||||||||||
Medical condition: The intended indication is Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Completed) SE (Completed) DK (Completed) GB (GB - no longer in EU/EEA) IE (Completed) PL (Completed) AT (Completed) HU (Completed) DE (Completed) SK (Completed) CZ (Completed) GR (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003340-72 | Sponsor Protocol Number: 5172-39 | Start Date*: 2013-05-14 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp. | |||||||||||||
Full Title: A Phase II Randomized Clinical Trial to Study the Efficacy and Safety of MK-5172 in Combination with Ribavirin (RBV) in Subjects with Chronic Hepatitis C Virus Infection | |||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006014-41 | Sponsor Protocol Number: Vasovist MA-01 | Start Date*: 2008-04-14 | |||||||||||
Sponsor Name:University Heidelberg, University Hospital Mannheim | |||||||||||||
Full Title: Determination of Diagnostic Accuracy and Added Value of Vasovist®-Enhanced Peripheral MRA in Comparison to Intra-arterial Digital Subtraction Angiography (i.a. DSA) in Patients with Peripheral Arte... | |||||||||||||
Medical condition: Patients suffering from PAOD stage III or stage IV (confirmed by ECCM MRA, CTA, non-selective DSA, DUS) and have an indication for the evaluation of the entire lower leg axis down to the feet (comm... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003802-30 | Sponsor Protocol Number: OMO-103-01 | Start Date*: 2022-09-21 | ||||||||||||||||||||||||||
Sponsor Name:Peptomyc S.L. | ||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study to evaluate the Safety, Pharmacokinetics, and Anti-Tumour Activity of the Myc Inhibitor OMO-103 administered intravenously in Patients with Advanced Tumours. | ||||||||||||||||||||||||||||
Medical condition: Solid tumours | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003874-17 | Sponsor Protocol Number: PrEPC/INMI | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS | |||||||||||||
Full Title: Antiretroviral Pre-exposure prophylaxis for natural conception (PrEP-C) in serodiscordant female partners of HIV-infected men in sustained virologic suppression | |||||||||||||
Medical condition: Prophylaxis against HIV infection | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004827-30 | Sponsor Protocol Number: RASLOW | Start Date*: 2017-03-21 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "BIANCHI-MELACRINO-MORELLI" | |||||||||||||
Full Title: RAPID VERSUS SLOW WITHDRAWAL OF ANTIEPILEPTIC MONOTHERAPY IN TWO-YEAR SEIZURE-FREE ADULTS PATIENTS WITH EPILEPSY (RASLOW) STUDY: A PRAGMATIC MULTICENTRE, PROSPECTIVE, RANDOMIZED, CONTROLLED STUDY. | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003300-31 | Sponsor Protocol Number: 20159460(c) | Start Date*: 2017-06-13 | |||||||||||
Sponsor Name:Hellenic Society for the Study of Bone Metabolism | |||||||||||||
Full Title: Evaluation of the efficacy of Denosumab in adult patients with Langerhans Cell Histiocytosis (LCH) : a multiple-site, single arm, open label Clinical Trial. | |||||||||||||
Medical condition: Langerhans Cell Histiocytosis (LCH) is a rare disease of unknown etiology with variable clinical course exhibiting both neoplastic and inflammatory features. It is characterized by the accumulatio... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004406-18 | Sponsor Protocol Number: INRCA-2017-01 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:IRCC INRCA | |||||||||||||
Full Title: Geriatric outcomes among older Type 2 diabetic patients treated with DPP4 inhibitors or glinides: focus on pro-inflammatory and oxidative stress markers (GOOD-WP1) | |||||||||||||
Medical condition: TYPE 2 DIABETES | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003769-14 | Sponsor Protocol Number: FIL_DLCL10 | Start Date*: 2012-09-27 | |||||||||||
Sponsor Name:Fondazione Italiana Linfomi ONLUS | |||||||||||||
Full Title: R-CHOP-14 or R-CHOP-21 & consolidation PET–oriented radiotherapy (RT) in diffuse large B cell lymphoma (DLBCL) patients with low risk profile according to age-adjusted IPI (0 with bulky or 1) | |||||||||||||
Medical condition: Patient with diffuse large B cell lymphoma (DLBCL) with low risk profile according to age-adjusted IPI (0 with bulky or 1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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