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Latest Trials
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 |
EudraCT Number: 2019-004511-31 | Sponsor Protocol Number: cASPerCF_2007_OPBG_2019 | Start Date: | |||||||||||
Sponsor Name: Bambino Gesù Children's Hospital | |||||||||||||
Full Title: Prospective validation and clinical evaluation of a new posaconazole dosing regimen for children and adolescents with cystic fibrosis and Aspergillus infection. | |||||||||||||
Medical condition: Cystic Fibrosis and Aspergillus Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Prematurely Ended) PT (Prematurely Ended) GR (Prematurely Ended) FR (Prematurely Ended) NL (Prematurely Ended) IE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003139-50 | Sponsor Protocol Number: Maxillo1 | Start Date: | ||||||
Sponsor Name: University of Bergen, Faculty of medicin and dentistry, Dep. of Clinical Dentistry | ||||||||
Full Title: International, multicenter phase II uncontrolled prospective clinical trial: Jaw bone reconstruction using a combination of biomaterial and autologous mesenchymal stem cells prior to dental impla... | ||||||||
Medical condition: Men and women aged 18 years or more requiring jaw bone reconstruction prior to dental implant placement based on clinical and radiological examinations (CBCT Cone beam CT imaging). Areas suitable ... | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: NO (Ongoing) | ||||||||
Trial results: (No results available) |