- 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 1,060 of 2,219.
| EudraCT Number: 2014-005448-17 | Sponsor Protocol Number: TMC435HPC1010 | Start Date*: 2015-04-09 | |||||||||||
| Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
| Full Title: A Phase 1, open-label, randomized, 2-panel, 3-way crossover study in healthy adult subjects to assess the relative bioavailability of simeprevir following single dose administration of age-appropri... | |||||||||||||
| Medical condition: Chronic Hepatitus C Virus (HCV) Infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003401-15 | Sponsor Protocol Number: D2560C00007 | Start Date*: 2015-03-24 |
| Sponsor Name:AstraZeneca K.K. | ||
| Full Title: A Phase 3 Open-label Study to Evaluate the Safety of MEDI3250 in Healthy Japanese Children age 2 years through 6 years | ||
| Medical condition: Healthy Children | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004844-37 | Sponsor Protocol Number: ACG-CR-065-2013 | Start Date*: 2015-07-16 |
| Sponsor Name:Enrique de Madaria Pascual | ||
| Full Title: A Randomized Controlled Pilot Trial of Indomethacin in Acute Pancreatitis | ||
| Medical condition: Acute pancreatitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005062-30 | Sponsor Protocol Number: NF001 | Start Date*: 2015-06-02 |
| Sponsor Name:University Hospital Germans Trias i Pujol | ||
| Full Title: Randomized, double-blind, placebo controlled clinical trial to assess the phrenic nerve functional status after periphrenic lidocaine infiltration in lung resection surgery. | ||
| Medical condition: Ipsilateral shoulder pain after thoracotomy for lung resection. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000475-27 | Sponsor Protocol Number: I14041 | Start Date*: 2015-07-29 | |||||||||||
| Sponsor Name:CHU de Limoges | |||||||||||||
| Full Title: Multicenter phase II trial of Nintedanib plus docetaxel in second line of treatment in patients with no squamous non small cell lung cancer refractory to first line chemotherapy (REFRACT study) | |||||||||||||
| Medical condition: No squamous non small cell lung | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000898-68 | Sponsor Protocol Number: 2013/VCC/0008 | Start Date*: 2014-01-24 | ||||||||||||||||||||||||||
| Sponsor Name:Velindre NHS Trust | ||||||||||||||||||||||||||||
| Full Title: A phase 1b/2 randomised placebo controlled trial of fulvestrant +/- AZD5363 in postmenopausal women with advanced breast cancer previously treated with a third generation aromatase inhibitor. | ||||||||||||||||||||||||||||
| Medical condition: Estrogen receptor positive advanced 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: 2014-004778-41 | Sponsor Protocol Number: RTA255-P001 | Start Date*: 2015-07-30 | ||||||||||||||||
| Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
| Full Title: Assessment of Anatomical and Functional Outcomes in Subjects Treated with Ocriplasmin for Vitreomacular Traction/Symptomatic Vitreomacular Adhesion (VMT/sVMA) | ||||||||||||||||||
| Medical condition: Vitreomacular Traction/ Vitreomacular Adhesion | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GR (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-001804-12 | Sponsor Protocol Number: ISA-HPV-01-12 | Start Date*: 2016-12-01 | |||||||||||
| Sponsor Name:ISA Therapeutics B.V. | |||||||||||||
| Full Title: A multicenter, open label Phase I/II study to determine the safety and immune modulating effects of the therapeutic Human Papilloma Virus Type 16 (HPV16) E6/E7 Synthetic Long Peptides Vaccine (ISA1... | |||||||||||||
| Medical condition: Patients with advanced (Stage IIIb-IVa with involvement of lymph nodes beyond the renal vein) or metastatic (stage IVb) or recurrent HPV16 positive cervical cancer for whom no curative treatment op... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003449-15 | Sponsor Protocol Number: 301012-CS5 | Start Date*: 2007-07-12 | |||||||||||
| Sponsor Name:Genzyme Europe B.V. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of ISIS 301012 as Add-on Therapy in Homozygous Familial Hypercholesterolemia Subjects | |||||||||||||
| Medical condition: Reduction of low density lipoprotein C (LDL-C) in Homozygous Familial Hypercholesterolemia (HoFH) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005327-27 | Sponsor Protocol Number: KOR15.1 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Robugen GmbH [...] | ||
| Full Title: Effects of Korodin Herz-Kreislauf-Tropfen on low blood pressure and cognitive functions in adolescents | ||
| Medical condition: low blood pressure | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000841-22 | Sponsor Protocol Number: HZA107112 | Start Date*: 2015-08-04 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: A randomised, double-blind, two-way crossover study to investigate the effect of inhaled fluticasone furoate on short-term growth in paediatric subjects with asthma | |||||||||||||
| Medical condition: Chronic disease of the lungs characterized by airway inflammation, bonchoconstriction and increased airway responsiveness. | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000120-28 | Sponsor Protocol Number: RSPR-007 | Start Date*: 2015-03-19 | |||||||||||
| Sponsor Name:RSPR Pharma AB | |||||||||||||
| Full Title: A Double-Blind, Randomised, Placebo-controlled, Cross-over, Phase 2 Mannitol Challenge Study, Investigating the Efficacy of CRD007 in Adult Subjects with Asthma | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002319-41 | Sponsor Protocol Number: HULP-VIR-2014-01 | Start Date*: 2015-05-11 | |||||||||||
| Sponsor Name:Ana Boto de los Bueis | |||||||||||||
| Full Title: Clinical and virologic assesment of two therapeutic options: antiviral Ganciclovir 0.15% ophthalmic gel and physiologic saline solution 0.9% used in patients with acute adenoviral conjuntivitis. | |||||||||||||
| Medical condition: Acute adenoviral conjunctivitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004398-18 | Sponsor Protocol Number: SP0756 | Start Date*: 2015-03-18 | |||||||||||
| Sponsor Name:UCB BIOSCIENCES, Inc. | |||||||||||||
| Full Title: An Open-label Extension Trial to Determine Safety and Efficacy of Long-term Oral SPM 927 in Patients With Partial Seizures | |||||||||||||
| Medical condition: Partial Epilepsies | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002806-30 | Sponsor Protocol Number: M1-1188_203 | Start Date*: 2014-12-09 | |||||||||||
| Sponsor Name:Takeda Development Centre Europe Ltd. | |||||||||||||
| Full Title: A Multi-Centre, Randomized, Double-Blind, Placebo-Controlled, Dose-Finding and Proof of Concept Study, to Assess the Efficacy, Safety and Tolerability, Pharmacokinetics and Pharmacodynamics of Nami... | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LV (Completed) DK (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004851-19 | Sponsor Protocol Number: AAPSMCS1002 | Start Date*: 2014-07-29 |
| Sponsor Name:ACORN Research, LLC | ||
| Full Title: A Phase II Study of Pazopanib in the Treatment of Surgically Unresectable or Metastatic Chondrosarcoma. | ||
| Medical condition: Surgically unresectable or metastatic chondrosarcoma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005567-33 | Sponsor Protocol Number: MEIN/14/FEB-PWV/001 | Start Date*: 2015-09-11 | |||||||||||
| Sponsor Name:Menarini International Operations Luxembourg S.A. | |||||||||||||
| Full Title: The Effect of Intensive Urate Lowering Therapy (ULT) with Febuxostat in Comparison with Allopurinol on Cardiovascular Risk in Patients with Gout Using Surrogate Markers: a Randomized, Controlled Tr... | |||||||||||||
| Medical condition: Gout | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) PL (Completed) HR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004181-21 | Sponsor Protocol Number: B1851056 | Start Date*: 2015-04-09 | |||||||||||
| Sponsor Name:Pfizer Japan, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Active-Controlled, Double-Blind Trial Evaluating the Safety, Tolerability, and Immunogenicity of a 13-valent Pneumococcal Conjugate Vaccine Given With DTaP Compared to Open-L... | |||||||||||||
| Medical condition: Prevention of disease caused by a type of bacteria called Streptococcus pneumoniae (pneumococcal disease). | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000254-64 | Sponsor Protocol Number: 114056 | Start Date*: 2012-04-12 | ||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
| Full Title: A phase III, open, controlled study to evaluate the immunogenicity, safety and reactogenicity of GSK Biologicals’ 10- valent pneumococcal conjugate vaccine administered to children with sickle cell... | ||||||||||||||||||
| Medical condition: Active immunization against disease caused by Streptococcus pneumoniae in children from 8 weeks up to 2 years of age. | ||||||||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-000176-10 | Sponsor Protocol Number: CSLCT-CAL-09-62 | Start Date*: 2015-03-23 |
| Sponsor Name:CSL Limited | ||
| Full Title: A Phase II, Multicenter, Randomized, Observer-blind, Placebo-controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of CSL’s 2009 H1N1 Influenza Vaccine (CSL425) in a Healthy Pedi... | ||
| Medical condition: Influenza, human. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
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