- 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 3 of 2,219.
| EudraCT Number: 2013-003301-26 | Sponsor Protocol Number: IAFIPF001 | Start Date*: 2013-09-20 | |||||||||||
| Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: A randomised placebo-controlled pilot trial of omeprazole in idiopathic pulmonary fibrosis (IPF) | |||||||||||||
| Medical condition: Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003644-12 | Sponsor Protocol Number: 2014-003644-12 | Start Date*: 2015-02-20 | |||||||||||||||||||||
| Sponsor Name:Neuromuscular Research Unit, Rigshospitalet | |||||||||||||||||||||||
| Full Title: The effect of Triheptanoin in adults with McArdle Disease (Glycogen Storage Disease Type V) | |||||||||||||||||||||||
| Medical condition: McArdle Disease Also called: Glycogen Storage Disease Type V or Myophosphorylase Deficiency | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-000494-36 | Sponsor Protocol Number: AC-083-103 | Start Date*: 2017-07-26 |
| Sponsor Name:Idorsia Pharmaceuticals Ltd | ||
| Full Title: A Phase 2a, multi-center, single-blind, within-subject, placebo-controlled study to assess the pharmacodynamics of ACT-709478 in subjects with photosensitive epilepsy | ||
| Medical condition: Photosensitive epilepsy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003503-29 | Sponsor Protocol Number: D5553C00003 | Start Date*: 2014-12-16 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A 28-week, Multicenter, Randomized, Double-Blind, Active-Controlled, Phase 3 Study with a 24-week Extension Phase Followed by a 52-week Extension Phase to Evaluate the Efficacy and Safety of Simult... | |||||||||||||
| Medical condition: Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004909-33 | Sponsor Protocol Number: LCTU122 | Start Date*: 2015-09-21 | ||||||||||||||||
| Sponsor Name:Manchester University NHS Foundation Trust | ||||||||||||||||||
| Full Title: Thrombin Inhibition Preoperatively in Early Breast Cancer | ||||||||||||||||||
| Medical condition: Breast Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-005406-11 | Sponsor Protocol Number: D1683C00005 | Start Date*: 2016-05-25 |
| Sponsor Name:Astrazeneca AB | ||
| Full Title: A Multi-Center, Randomized, Double-Blind, Active-Controlled, Parallel Group, Phase III Trial to Evaluate the Safety and Efficacy of Saxagliptin 5mg Co-administered with Dapagliflozin 5mg compared t... | ||
| Medical condition: Type 2 diabetes mellitus, inadequate glycaemic control | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-005543-90 | Sponsor Protocol Number: 20130108 | Start Date*: 2014-08-26 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Randomized, Double-Blind Study to Compare Pharmacokinetics and Pharmacodynamics, Efficacy and Safety of ABP 798 With Rituximab in Subjects With Moderate to Severe Rheumatoid Arthritis | |||||||||||||
| Medical condition: Rheumatoid arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) PL (Completed) BG (Completed) EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000376-26 | Sponsor Protocol Number: ZPL521/101 | Start Date*: 2016-05-09 | |||||||||||
| Sponsor Name:Ziarco Pharma Ltd | |||||||||||||
| Full Title: A Randomised, Adaptive Design, Double-Blind (3rd Party Open), Placebo Controlled, Sequential Group Study to Determine the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Applica... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002449-31 | Sponsor Protocol Number: ZP4207-16137 | Start Date*: 2018-02-16 | |||||||||||
| Sponsor Name:Zealand Pharma A/S | |||||||||||||
| Full Title: A phase 3, randomized, double-blind, parallel trial to confirm the clinical efficacy and safety of dasiglucagon in the rescue treatment of hypoglycemia in subjects with type 1 diabetes mellitus (T1... | |||||||||||||
| Medical condition: Type 1 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005674-37 | Sponsor Protocol Number: COL-MIG-305(H8H-CD-LAHL) | Start Date*: 2016-11-01 | |||||||||||||||||||||||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||||||||||||||||||||||
| Full Title: An Open-label, LonG-term, Safety Study of LAsmiDItan (100 mg and 200 mg) in the Acute Treatment Of MigRaine (GLADIATOR) | |||||||||||||||||||||||||||||||||
| Medical condition: acute migraine | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-000593-38 | Sponsor Protocol Number: MR308-3502 | Start Date*: 2016-12-05 | |||||||||||
| Sponsor Name:Mundipharma Research GmbH & Co. KG | |||||||||||||
| Full Title: A Randomized, Double-Blind, Multicenter, Placebo- and active Comparator-Controlled Study to evaluate Efficacy and Safety of MR308 in the Treatment of Acute Pain After Abdominal Hysterectomy Surgery... | |||||||||||||
| Medical condition: Acute pain after open total or subtotal abdominal hysterectomy | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) SK (Completed) LV (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004615-45 | Sponsor Protocol Number: BPR-PIP-002 | Start Date*: 2016-12-02 | ||||||||||||||||
| Sponsor Name:Basilea Pharmaceutica International Ltd | ||||||||||||||||||
| Full Title: A multicentre, randomized, investigator-blind, active-controlled study to evaluate the safety, tolerability, pharmacokinetics and efficacy of ceftobiprole versus intravenous standard-of-care cephal... | ||||||||||||||||||
| Medical condition: Hospital-acquired pneumonia or community-acquired pneumonia requiring hospitalisation. | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) BG (Completed) Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-001351-31 | Sponsor Protocol Number: ED17/93260 | Start Date*: 2017-09-04 | |||||||||||
| Sponsor Name:University of Leeds | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled phase II pilot trial investigating efficacy, safety and feasibility of 11β-hydroxysteroid dehydrogenase type 1 inhibition by AZD4017 to improve skin f... | |||||||||||||
| Medical condition: Type 2 diabetes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000724-10 | Sponsor Protocol Number: 60978 | Start Date*: 2018-07-04 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Targeting esophageal cancer with HDL nanoparticles: an imaging study | ||
| Medical condition: Primary esophageal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001223-31 | Sponsor Protocol Number: KAISII | Start Date*: 2016-10-11 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Incidence of Invasive Fungal Disease in Patients receiving Immunosuppressive Therapy, Intensive Chemotherapy or Reduced Intensity Haematopoietic Stem Cell Transplantation on Posaconazole Prophylaxis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Aplastic Anaemia, Myelodysplastic syndromes, Acute Myeloid Leukaemia undergoing immunosuppression therapy, high dose chemotherapy or reduced intensity stem cell transplantation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-001853-41 | Sponsor Protocol Number: 57698 | Start Date*: 2018-09-19 | ||||||||||||||||||||||||||
| Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||
| Full Title: Intensive endoscopic therapy versus conventional treatment for untreated benign anastomotic strictures after esophagectomy: a pilot and randomized controlled trial | ||||||||||||||||||||||||||||
| Medical condition: Benign esophagogastric anastomotic strictures after esophagectomy | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-002209-39 | Sponsor Protocol Number: M14LTK | Start Date*: 2014-07-30 |
| Sponsor Name:The Netherlands Cancer Institute | ||
| Full Title: Phase I/II study with lapatinib plus trametinib in patients with metastatic KRAS mutant non-small cell lungcancer | ||
| Medical condition: non-small cell lung cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004529-17 | Sponsor Protocol Number: YO39609 | Start Date*: 2018-07-17 | ||||||||||||||||
| Sponsor Name:F. Hoffman-La Roche Ltd | ||||||||||||||||||
| Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER, RANDOMIZED, UMBRELLA STUDY EVALUATING THE EFFICACY AND SAFETY OF MULTIPLE IMMUNOTHERAPY-BASED TREATMENT COMBINATIONS IN PATIENTS WITH LOCALLY ADVANCED UNRESE... | ||||||||||||||||||
| Medical condition: Locally advanced unresectable or Metastatic gastric or gastroesophageal junction cancer or esophageal cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-004898-32 | Sponsor Protocol Number: SAM103848 | Start Date*: 2016-12-08 |
| Sponsor Name:GlaxoSmithKline Research & Development Ltd. | ||
| Full Title: Pediatric Asthma Clinical Effectiveness study (PEACE). A Randomized, Double-Blind, Double Dummy, Parallel Group comparative clinical study of Salmeterol/Fluticasone propionate Inhalation Powder (50... | ||
| Medical condition: Asthma | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2016-005083-34 | Sponsor Protocol Number: CAPI2017NL10 | Start Date*: 2017-08-23 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Conestat alfa as prophylactic treatment for idiopathic non-histaminergic acquired angioedema | ||
| Medical condition: The medical condition to be investigated is idiopathic non-histaminergic angioedema (InH-AAE). This disease is characterized by recurrent episodes with swelling of the subcutis and mucous membranes... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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