- Trials with a EudraCT protocol (331)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
331 result(s) found for: Clinical Guideline.
Displaying page 1 of 17.
| EudraCT Number: 2022-003526-50 | Sponsor Protocol Number: HACOL-ACS | Start Date*: 2023-05-09 | ||||||||||||||||
| Sponsor Name:Hannover Medical School | ||||||||||||||||||
| Full Title: A prospective, interventional, single-center, single-arm study to assess the effectiveness of Bempedoic acid to achieve LDL-cholesterol targets in patients following ST-elevation or Non-ST-elevatio... | ||||||||||||||||||
| Medical condition: Patients following acute percutaneous coronary intervention for STEMI or NSTEMI insufficiently treated with high-intensity oral lipid lowering therapy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-014913-28 | Sponsor Protocol Number: 09_056R | Start Date*: 2011-02-03 |
| Sponsor Name:London School of Hygiene & Tropical Medicine | ||
| Full Title: RETRO-PRO: The effectiveness of simvastatin compared to atorvastatin: an e-clinical randomised trial within a research database in routine clinical practice - a feasibility study | ||
| Medical condition: subjects who in the opinion of the GP investigator would require a statin for primary prevention according to the 2008 NICE guideline on lipid modification: adults over 40 who have a 20% or greater... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002823-86 | Sponsor Protocol Number: ENCHANTED | Start Date*: 2015-02-04 |
| Sponsor Name:The George Institute for Global Health Australia | ||
| Full Title: Enhanced Control of Hypertension and Thrombolysis Stroke Study | ||
| Medical condition: Acute ischaemic stroke | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003061-38 | Sponsor Protocol Number: NL82555.100.22 | Start Date*: 2023-05-02 |
| Sponsor Name:Sint Antonius Ziekenhuis | ||
| Full Title: Genotype-gUIded cLopidogrel monoTherapY (POPular GUILTY) | ||
| Medical condition: Non-ST elevation acute coronary syndrome (coronary artery disease) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002718-17 | Sponsor Protocol Number: IMVT-1401-2401 | Start Date*: 2023-06-19 | |||||||||||
| Sponsor Name:Immunovant Sciences, GmbH | |||||||||||||
| Full Title: A Phase 2b, Multi-center, Randomized, Quadruple-blind, Placebo-controlled Study of Batoclimab Treatment in Adult Participants with Active Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
| Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) NO (Trial now transitioned) BE (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) DK (Trial now transitioned) SK (Trial now transitioned) PT (Trial now transitioned) BG (Trial now transitioned) ES (Ongoing) RO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004133-16 | Sponsor Protocol Number: IH141 | Start Date*: 2015-02-19 |
| Sponsor Name:Hull and east Yorkshire Hospitals Trust | ||
| Full Title: Exploratory multicentre prospective double blinded randomised controlled pilot study of the effect of intravenous iron supplementation(Monofer)in iron deficient but not anaemic patients with Chroni... | ||
| Medical condition: Chronic Kidney Disease stages 3b to 5 with iron deficiency | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-003570-49 | Sponsor Protocol Number: KB065 | Start Date*: 2021-02-05 | |||||||||||
| Sponsor Name:Kedrion S.p.A. | |||||||||||||
| Full Title: Phase III, Open-label, Uncontrolled, Multicenter Study to Assess Efficacy, Pharmacokinetics and Safety of IMMUNORHO in the Prevention of RhD Isoimmunization in Rh(D) negative Women Pregnant with Rh... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000776-16 | Sponsor Protocol Number: JM-2005-1 | Start Date*: 2007-08-20 |
| Sponsor Name:Masaryk University | ||
| Full Title: Development of Tumor Infiltrating Lymphocytes in Patients with Metastatic melanoma | ||
| Medical condition: Patient with Metastatic melanoma in IV (clinical) stage of disease. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-013671-21 | Sponsor Protocol Number: V111_02 | Start Date*: 2009-08-27 |
| Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
| Full Title: A Randomized, Single-blind, Dose-Ranging, Study to Evaluate Immunogenicity, Safety and Tolerability of Different Formulations of Adjuvanted and non Adjuvanted Egg-Derived, Inactivated Novel Swine O... | ||
| Medical condition: Pandemic influenza | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) DE (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003564-37 | Sponsor Protocol Number: PRN1008-005 | Start Date*: 2016-04-21 | |||||||||||
| Sponsor Name:Principia Biopharma Australia Pty Ltd | |||||||||||||
| Full Title: An Open-Label, Phase 2, Pilot Study Investigating the Safety, Clinical Activity, Pharmacokinetics, and Pharmacodynamics of Oral Treatment with the BTK Inhibitor PRN1008 in Patients with Newly Diagn... | |||||||||||||
| Medical condition: Pemphigus: Pemphigus Vulgaris | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002177-11 | Sponsor Protocol Number: 80-83600-98-20013 | Start Date*: 2015-04-16 |
| Sponsor Name:ZonMW GGG | ||
| Full Title: Step-down versus step-up analgesics in patients with (sub)acute sciatica in primary care | ||
| Medical condition: Patients with (sub)acute sciatica in primary care. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005182-14 | Sponsor Protocol Number: A-20-1013-C-03 | Start Date*: 2021-02-25 | |||||||||||
| Sponsor Name:Alligator Bioscience AB | |||||||||||||
| Full Title: An open-label phase 1b/2 study assessing the safety and efficacy of mitazalimab in combination with chemotherapy in patients with metastatic pancreatic ductal adenocarcinoma | |||||||||||||
| Medical condition: Metastatic Pancreatic Ductal Adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000021-27 | Sponsor Protocol Number: ZN-c3-003 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:K-Group Beta | |||||||||||||
| Full Title: A Phase 1/2 Dose Escalation and Dose Expansion Study of ZN-c3 in Combination with Gemcitabine in Adult and Pediatric Subjects with Relapsed or Refractory Osteosarcoma | |||||||||||||
| Medical condition: Relapsed or Refractory Osteosarcoma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) ES (Ongoing) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001817-40 | Sponsor Protocol Number: NAF 3.4.05.003 | Start Date*: 2007-05-10 |
| Sponsor Name:Netherlands Asthma Foundation (NAF) [...] | ||
| Full Title: An early diagnosis of asthma in young children by using non-invasive biomarkers of oxidative stress/airway inflammation | ||
| Medical condition: young children with recurrent respiratory symptoms | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004889-28 | Sponsor Protocol Number: FFR113342 | Start Date*: 2016-12-21 |
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Study to Evaluate the Efficacy and Safety of Fluticasone Furoate Nasal Spray for 2 Weeks in Chinese Adult and Adolescent... | ||
| Medical condition: Rhinitis, Allergic, Perennial | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2021-004161-13 | Sponsor Protocol Number: ZN-c3-006 | Start Date*: 2022-04-24 | |||||||||||
| Sponsor Name:K-Group Beta, Inc. | |||||||||||||
| Full Title: A Phase 1/2 Dose-Escalation and Dose-Expansion Study of ZN-c3 in Combination with Niraparib in Subjects with Platinum-Resistant Ovarian Cancer | |||||||||||||
| Medical condition: Platinum-resistant Ovarian Cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003429-41 | Sponsor Protocol Number: SOLTI-1909 | Start Date*: 2021-06-23 |
| Sponsor Name:SOLTI | ||
| Full Title: NiVOlumab for Luminal advanced/metastatic breast cancer to Taper ct-dnA In endocrine REsistance (VOLTAIRE trial) | ||
| Medical condition: NiVOlumab for Luminal advanced/metastatic breast cancer to Taper ct-dnA In endocrine REsistance | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004921-41 | Sponsor Protocol Number: P06332 | Start Date*: 2015-02-24 |
| Sponsor Name:Corporation Schering-Plough K.K. | ||
| Full Title: Multicenter, double-blind, randomized, placebo-controlled study of mometasone furoate nasal spray in pediatric subjects with perennial allergic rhinitis | ||
| Medical condition: perennial allergic rhinitis | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2004-003825-29 | Sponsor Protocol Number: 04/aaa1234. | Start Date*: 2005-06-06 |
| Sponsor Name:Cardiff and Vale NHS Trust | ||
| Full Title: MAGNET - a randomised placebo controlled trial of the use of nebulised magnesium sulphate in moderate/severe acute asthma in childhood | ||
| Medical condition: MAGNET is a randomised placebo(isotonic saline) controlled trial of the use of nebulised magnesium sulphate in moderate/severe acute asthma in childhood. All children (2-16 years of age) presenting... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005545-12 | Sponsor Protocol Number: | Start Date*: 2012-03-02 | |||||||||||
| Sponsor Name:University of Leicester | |||||||||||||
| Full Title: Enhanced Control of Hypertension and Thrombolysis Stroke Trial | |||||||||||||
| Medical condition: Acute Ischaemic Stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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