- 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 1,388 of 2,219.
| EudraCT Number: 2018-002589-38 | Sponsor Protocol Number: NN9924-4309 | Start Date*: 2019-08-26 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: PIONEER 12 China multi-regional clinical trial: Efficacy and safety of oral semaglutide versus sitagliptin in subjects with type 2 diabetes mellitus treated with metformin | |||||||||||||
| Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) RO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002597-44 | Sponsor Protocol Number: CFZ004 | Start Date*: 2014-02-10 | |||||||||||
| Sponsor Name:Onyx Therapeutics, Inc. | |||||||||||||
| Full Title: Phase 1b/2, Multicenter, Open-label Study of Carfilzomib, Carboplatin, and Etoposide in Subjects with Previously Untreated Extensive-stage Small-cell Lung Cancer | |||||||||||||
| Medical condition: Untreated extensive stage small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) FR (Completed) HU (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002834-59 | Sponsor Protocol Number: SNFCT2015-05 | Start Date*: 2016-11-28 | |||||||||||||||||||||
| Sponsor Name:Sanifit Therapeutics S.A. | |||||||||||||||||||||||
| Full Title: A double-blind, randomised, placebo-controlled study to assess the effect of SNF472 on progression of cardiovascular calcification on top of standard of care in end-stage-renal-disease (ESRD) patie... | |||||||||||||||||||||||
| Medical condition: Cardiovascular calcification in blood vessels in end-stage-renal-disease (ESRD) patients on haemodialysis (HD). | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-004162-13 | Sponsor Protocol Number: SAE-13/IBD | Start Date*: 2007-02-27 | |||||||||||
| Sponsor Name:Charité Universitätsmedizin, Campus Charité Mitte | |||||||||||||
| Full Title: Randomized, double-blind, placebo-controlled phase II pilot study of the impact of mesalazine enemas on the mucosal gut flora in patients with inflammatory bowel disease | |||||||||||||
| Medical condition: Active inflammatory bowel disease, i.e. either left-sided ulcerative colitis or Crohn´s Disease (Colon) with signs of inflammation within 40 cm ab ano. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000682-30 | Sponsor Protocol Number: 01-09.02.15. | Start Date*: 2015-04-27 | |||||||||||
| Sponsor Name:Tartu University Hospital | |||||||||||||
| Full Title: Botulinum neurotoxin type A treatment for sialorrhea in central nervous system diseases | |||||||||||||
| Medical condition: Hypersalivation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000211-99 | Sponsor Protocol Number: D1449L00010 | Start Date*: 2005-04-12 |
| Sponsor Name:AstraZeneca A/S | ||
| Full Title: Acutely Manic Patients Insufficiently Responding After 2 Weeks Continued Quetiapine Monotherapy: Continued Quetiapine Versus Sodium Valproate Add-on. | ||
| Medical condition: Bipolar affective disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016468-35 | Sponsor Protocol Number: D8480C00067 | Start Date*: 2016-03-29 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A randomised, double-blind, phase III efficacy and safety study of cediranib (RECENTIN™ ) when added to cisplatin plus a fluoropyrimidine, compared with cisplatin plus a fluoropyrimidine alone, in ... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Gastric cancer | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GR (Completed) HU (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2008-005578-12 | Sponsor Protocol Number: 08-PIR-06 | Start Date*: 2009-03-02 | |||||||||||
| Sponsor Name:Nektar Therapeutics | |||||||||||||
| Full Title: A Multicenter, Open-Label, Phase 2 Study to Evaluate the Safety and Efficacy of NKTR-102 (PEG-Irinotecan) When Given on a Q14 Day or a Q21 Day Schedule in Patients with Metastatic or Locally Advanc... | |||||||||||||
| Medical condition: Patients with Metastatic or Locally Advanced Cervical Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004229-93 | Sponsor Protocol Number: D791AC00008 | Start Date*: 2004-12-20 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: Multicentre, open label, extension study of treatment with gefitinib (IRESSA™) for patients completing other gefitinib clinical studies who may benefit from gefitinib treatment | ||
| Medical condition: This trial is for patients with advanced non-small cell lung cancer who have completed a preceding gefitinib trial (ZD1839IL0709 or ZD1839IL0710) and in the opinion of the investigator may benefit ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) EE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002890-71 | Sponsor Protocol Number: RifaxNK150612 | Start Date*: 2012-08-16 | |||||||||||
| Sponsor Name:Flemming Bendtsen | |||||||||||||
| Full Title: Intestinal decontamination with rifaximin. Effects on the inflammatory and circulatory state in patients with cirrhosis and ascites - A randomised controlled clinical study | |||||||||||||
| Medical condition: Liver cirrhosis of any etilogy, complicated by decompensation and classified as Child-Pugh B or C | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006250-25 | Sponsor Protocol Number: D8480C00034 | Start Date*: 2008-02-29 | ||||||||||||||||
| Sponsor Name:ASTRAZENECA | ||||||||||||||||||
| Full Title: A Phase III, Randomised, Double-blind, Multi-centre, Parallel Group Study to Compare the Efficacy of Cediranib (AZD2171, RECENTIN™) (30 mg) When Added to Gemcitabine and Cisplatin versus the Effica... | ||||||||||||||||||
| Medical condition: Locally Advanced or Metastatic (Stage IIIb/IV) Non Small Cell Lung Cancer. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) SK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001646-10 | Sponsor Protocol Number: ANIMAL-523-2014-2569 | Start Date*: 2017-06-22 |
| Sponsor Name:Uppsala University Hospital | ||
| Full Title: Anesthesia Induced Hormonal Oliguria Trial | ||
| Medical condition: Anaesthesia in adult patients undergoing general surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-003829-16 | Sponsor Protocol Number: RV-MM-DSMM-0279 | Start Date*: 2009-09-15 | |||||||||||
| Sponsor Name:GMIHO - Gesellschaft für medizinische Innovation Hämatologie und Onkologie mbH | |||||||||||||
| Full Title: An open, randomized clinical phase I/II trial to investigate maximum tolerated dose, efficacy, and safety of lenalidomide/low-dose dexamethasone in combination with continuous oral cyclophosphamide... | |||||||||||||
| Medical condition: relapsed multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001518-34 | Sponsor Protocol Number: ML20296 | Start Date*: 2006-07-17 |
| Sponsor Name:Roche Farma, S.A. | ||
| Full Title: Estudio fase II abierto, no aleatorizado, de erlotinib en combinación con gemcitabina en pacientes con adenocarcinoma de páncreas avanzado irresecable o metastásico: relación entre rash cutáneo y ... | ||
| Medical condition: Adenocarcinoma de páncreas avanzado irresecable o metastásico [Advanced unresectable or metastatic adenocarcinoma of the pancreas]. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012541-33 | Sponsor Protocol Number: D5127C00001 | Start Date*: 2009-08-11 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A randomised, placebo-controlled, double-blind (double-dummy technique), crossover, multi-centre study, to evaluate onset of effect in patients with Chronic Obstructive Pulmonary Disease (COPD) tre... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004338-26 | Sponsor Protocol Number: FE200486 CS28 | Start Date*: 2008-11-18 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: Ensayo clínico abierto, aleatorizado, de grupos paralelos que compara degarelix frente a bloqueo androgénico combinado (goserelina + bicalutamida) en términos de reducción de la puntuación en la es... | |||||||||||||
| Medical condition: Cáncer de próstata | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-000145-58 | Sponsor Protocol Number: N01306 | Start Date*: 2008-07-11 | |||||||||||
| Sponsor Name:UCB Pharma S.A. | |||||||||||||
| Full Title: An international, double-blind, randomized, multi-center, parallel group, historical-control conversion to monotherapy study to evaluate the efficacy and safety of brivaracetam in subjects (≥ 16 to... | |||||||||||||
| Medical condition: Partial onset seizures with or without secondary generalization. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Completed) HU (Prematurely Ended) FI (Prematurely Ended) FR (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004908-31 | Sponsor Protocol Number: PM2734-B-001-08 | Start Date*: 2008-11-18 | |||||||||||
| Sponsor Name:Pharma Mar S.A. | |||||||||||||
| Full Title: Ensayo clínico y farmacocinético de fase II de infusión de 30 minutos de PM02734 (Irvalec®) cada tres semanas en pacientes con cáncer no microcítico de pulmón (CNMP) epidermoide previamente tratado... | |||||||||||||
| Medical condition: Cáncer no microcítico de pulmón (CNMP) epidermoide | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004183-38 | Sponsor Protocol Number: A3241010 | Start Date*: 2008-11-19 | |||||||||||
| Sponsor Name:Pfizer, S.A. | |||||||||||||
| Full Title: ENSAYO ALEATORIZADO, CONTROLADO CON PLACEBO PARA EVALUAR LA EFICACIA, LA SEGURIDAD Y LA TOLERABILIDAD DE CP 533,536 EN PACIENTES CON FRACTURA CERRADA DE LA DIAFASIS TIBIAL A RANDOMIZED, PLACEBO-CON... | |||||||||||||
| Medical condition: consolidación ósea | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000904-33 | Sponsor Protocol Number: 108-PR-PRI-147 | Start Date*: 2008-05-07 |
| Sponsor Name:LABORATORIOS LETI, S.L.U | ||
| Full Title: Extracto alergénico de Glycyphagus domesticus. Determinación de la potencia alergénica in vivo en unidades equivalentes de histamina (HEP) | ||
| Medical condition: Alergia frente a los acaros de "Glycyphagus domesticus" | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
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