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EudraCT Number: 2005-000346-36 | Sponsor Protocol Number: BPLG-004 | Start Date: | |||||||||||
Sponsor Name: BioPartners GmbH [...] 1. BioPartners GmbH 2. LG Life Science Ltd. | |||||||||||||
Full Title: A Phase III, Multi-centre, Randomised, Parallel Group Study of Safety and Efficacy of the LB03002 a New Sustained Release Formulation of Human Recombinant Growth Hormone as Compared to Standard Dai... | |||||||||||||
Medical condition: pre-pubertal drug naïve growth-deficient children with insufficient endogenous growth hormone secretion | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) FI (Prematurely Ended) SE (Prematurely Ended) SK (Completed) HU (Completed) CZ (Prematurely Ended) IT (Completed) DE (Completed) LT (Prematurely Ended) EE (Prematurely Ended) LV (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004093-40 | Sponsor Protocol Number: 08-PIR-03 | Start Date: | ||||||||||||||||
Sponsor Name: Nektar Therapeutics | ||||||||||||||||||
Full Title: A Multicenter, Open-Label, Randomized, Phase 2 Study to Evaluate the Efficacy and Safety of NKTR-102 (PEG-Irinotecan) Versus Irinotecan in Patients with Second-Line, Irinotecan-Naïve, KRAS-Mutant, ... | ||||||||||||||||||
Medical condition: Refractory Solid Tumors (Colorectal Cancer) Tumores sólidos refractarios (Cáncer colorrectal) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) BE (Prematurely Ended) DE (Completed) GB (Completed) SK (Completed) LV (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002686-18 | Sponsor Protocol Number: EP0162 | Start Date: | |||||||||||
Sponsor Name: UCB Biopharma SRL | |||||||||||||
Full Title: A Double-Blind, Randomized, Placebo-Controlled, Multicenter, Outpatient, Parallel-Group Study to Assess the Efficacy and Safety of Staccato Alprazolam in Study Participants 12 Years of Age and Olde... | |||||||||||||
Medical condition: Treatment of stereotypical prolonged seizure | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) FR (Ongoing) HU (Ongoing) CZ (Ongoing) ES (Ongoing) PL (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020386-24 | Sponsor Protocol Number: TRO19622CLEQ1275-1 | Start Date: | |||||||||||
Sponsor Name: TROPHOS SA | |||||||||||||
Full Title: Phase II, multicenter, randomized, adaptive, double-blind, placebo controlled study to assess safety and efficacy of olesoxime (TRO19622) in 3-25 year old Spinal Muscular Atrophy (SMA) patients. | |||||||||||||
Medical condition: Spinal Muscular Atrophy (type 2 or type 3 non ambulant patients aged 3-25 years) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) NL (Completed) BE (Completed) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004586-41 | Sponsor Protocol Number: CHUBX2012/16 | Start Date: | |||||||||||
Sponsor Name: CHU de Bordeaux | |||||||||||||
Full Title: Cognitive remediation in Attention Deficit Disorder with or without Hyperactivity (ADHD) children : Comparison between three therapeutic strategies : cognitive remediation with a virtual classroom ... | |||||||||||||
Medical condition: Attention Deficit Disorder with or without Hyperactivity | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002637-42 | Sponsor Protocol Number: EP0165 | Start Date: | |||||||||||
Sponsor Name: UCB Biopharma SRL | |||||||||||||
Full Title: An Open-Label, Multicenter, Outpatient Extension Study to Evaluate the Safety and Tolerability of Staccato Alprazolam in Study Participants 12 Years of Age and Older With Stereotypical Prolonged Se... | |||||||||||||
Medical condition: Treatment of stereotypical prolonged seizure | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) IT (Ongoing) FR (Not Authorised) HU (Ongoing) CZ (Ongoing) PL (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017267-41 | Sponsor Protocol Number: CQAV680A2201E1 | Start Date: | |||||||||||
Sponsor Name: Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, parallel group study to compare the pharmacodynamics/efficacy, safety and pharmacokinetics of QAV680 versus placebo in patients with moderate persistent asthma | |||||||||||||
Medical condition: Moderate persistent asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014768-21 | Sponsor Protocol Number: TUD-TEMDS1-042 | Start Date: | |||||||||||
Sponsor Name: Dresden Technical University | |||||||||||||
Full Title: Treatment of MDS patients with single agent temsirolimus – a pilot study | |||||||||||||
Medical condition: Myelodysplastic Syndromes (MDS) (20 IPSS LOW+INT-1 and 20 IPSS INT-2+HIGH or proliferating CMML) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021792-81 | Sponsor Protocol Number: 2010-12 | Start Date: | ||||||
Sponsor Name: ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||||||||
Full Title: SFCE-Metro 01 : Etude de phase II de chimiothérapie métronomique associant celecoxib-methotrexate-vinblastine-cyclophosphamide chez les enfants porteurs d’une tumeur solide en rechute ou en progre... | ||||||||
Medical condition: children and adolescents with relapsed or progressing solid tumours. | ||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: FR (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002270-29 | Sponsor Protocol Number: IN 0401 INT | Start Date: | |||||||||||
Sponsor Name: LEO Pharma A/S | |||||||||||||
Full Title: Safety profile of innohep versus subcutaneous unfractionated Heparin in elderly patients with impaired renal function treated for acute deep vein thrombosis | |||||||||||||
Medical condition: Treatment of acute deep vein thrombosis in elderly patients with impaired renal function | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) DK (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |