- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (410)
14 result(s) found for: ADE.
Displaying page 1 of 1.
EudraCT Number: 2010-022293-14 | Sponsor Protocol Number: ANRS146OPTIMAL | Start Date*: 2012-08-22 |
Sponsor Name:Inserm-ANRS | ||
Full Title: Optimized Phase III Trial of Immuno-stimulation with Maraviroc, a CCR5 antagonist, combined with Anti Retroviral Therapy (cART) in advanced, Late diagnosed HIV-1 infected patients with an AIDS-defi... | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002170-36 | Sponsor Protocol Number: 2014-002170-36 | Start Date*: 2015-02-11 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Treatment of Cervical Spinal Cord Injury with Imatinib – a safety and feasibility study | ||
Medical condition: Cervical Spinal Cord Injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003401-60 | Sponsor Protocol Number: CT-P59_3.1 | Start Date*: 2020-09-30 | |||||||||||
Sponsor Name:CELLTRION, Inc. | |||||||||||||
Full Title: A Phase 2/3, Randomized, Parallel-Group, Placebo-Controlled, Double-Blind Study to Evaluate the Efficacy and Safety of CT-P59 in Combination with Standard of Care in Hospitalized Patients with SARS... | |||||||||||||
Medical condition: Novel severe acute respiratory syndrome coronavirus 2 (SARS CoV 2) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005694-31 | Sponsor Protocol Number: 2012/ADE002 | Start Date*: 2013-07-05 | |||||||||||
Sponsor Name:Adenovir Pharma AB | |||||||||||||
Full Title: Evaluation of the Therapeutic Efficacy of APD-209 Eye Drops in Treatment of Acute Phase Adenoviral-Induced Epidemic Keratoconjunctivitis (EKC). A Randomised, Double-Masked, Placebo-Controlled, Mult... | |||||||||||||
Medical condition: Acute phase Adenoviral-induced Epidemic Keratoconjunctivitis, EKC | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000346-19 | Sponsor Protocol Number: HP-CD-CL-2003 | Start Date*: 2018-06-04 | |||||||||||
Sponsor Name:Herantis Pharma Plc | |||||||||||||
Full Title: A Randomised, Double-Blind, Multi-centre, Active Treatment, Extension and Safety Study for Patients with Idiopathic Parkinson’s Disease (PD) Who Previously Completed the CDNF/DDS Main Study HP-CD-C... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001685-35 | Sponsor Protocol Number: ADT-2022-003 | Start Date*: 2022-12-27 | |||||||||||
Sponsor Name:Adeptio Pharmaceuticals Limited | |||||||||||||
Full Title: Randomized, double-blind, placebo controlled clinical trial of (+)-α-dihydrotetrabenazine in patients with moderate to severe tardive dyskinesia. | |||||||||||||
Medical condition: Tardive dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) HU (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004062-17 | Sponsor Protocol Number: NEK/MD/0119 | Start Date*: 2020-12-03 |
Sponsor Name:Nekkar Lab srl | ||
Full Title: OPEN, COMPARATIVE STUDY TO EVALUATE THE PERFORMANCE AND SAFETY OF THE MEDICAL DEVICE MARIAL® IN ASSOCIATION WITH PROTON-PUMP INHIBITORS VERSUS PPI ALONE IN PATIENTS AFFECTED BY GASTROESOPHAGEAL REF... | ||
Medical condition: gastroesophageal reflux disease (GERD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004175-73 | Sponsor Protocol Number: HP-CD-CL-2002 | Start Date*: 2017-09-27 | |||||||||||
Sponsor Name:Herantis Pharma Plc | |||||||||||||
Full Title: A Phase I-II, Randomised, Double-Blind, Placebo Controlled, Safety and Tolerability Study of Intermittent Bilateral Intraputamenal Cerebral Dopamine Neurotrophic Factor (CDNF) Infusions Administere... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003369-20 | Sponsor Protocol Number: CT-P59_3.2 | Start Date*: 2020-11-13 | |||||||||||
Sponsor Name:Celltrion, Inc | |||||||||||||
Full Title: A Phase 2/3, Randomized, Parallel-group, Placebo-controlled, Double-Blind Study to Evaluate the Efficacy and Safety of CT-P59 in Combination with Standard of Care in Outpatients with Severe Acute R... | |||||||||||||
Medical condition: SARS CoV 2 infection in outpatients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) RO (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000720-19 | Sponsor Protocol Number: IDI01/2020 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:IDI FARMACEUTICI SRL | |||||||||||||
Full Title: A prospective, randomized, multicenter, open- label, two-arm and parallel-group Study to evaluate the efficacy and safety of Nicotinamide DS compared to Ciclopirox olamine cream at 1% in patients a... | |||||||||||||
Medical condition: Patients affected by seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000271-39 | Sponsor Protocol Number: 2022-01 | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:Adeptio Pharmaceuticals Ltd | |||||||||||||
Full Title: Single-arm, open-label dose titration phase 2 clinical trial of (+)-α-DHTBZ for the treatment of tardive dyskinesia (TD) | |||||||||||||
Medical condition: Tardive dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005170-19 | Sponsor Protocol Number: HP-CD-CL-2004 | Start Date*: 2018-07-30 | |||||||||||
Sponsor Name:Renishaw Neuro Solutions Ltd. | |||||||||||||
Full Title: A Long-Term Follow-up Safety Study for Patients with Idiopathic Parkinson’s Disease (PD) Implanted with the DDS and/or Who Received Treatment in the Main Study and/or Extension Study | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004891-28 | Sponsor Protocol Number: HM08 / 8451 | Start Date*: 2009-09-03 | ||||||||||||||||
Sponsor Name:Leeds Teaching Hospitals Trust | ||||||||||||||||||
Full Title: Pilot safety/tolerability study of Lenalidomide administered as monotherapy and in combination with standard chemotherapy for Acute Myeloid Leukaemia/high-risk myelodysplastic syndrome with structu... | ||||||||||||||||||
Medical condition: Acute myeloid leukaemia / high-risk Myelodysplastic Syndrome with structural abnormalities of chromosome 5 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004599-19 | Sponsor Protocol Number: INTERFANT-06 | Start Date*: 2005-11-24 | |||||||||||
Sponsor Name:A.I.E.O.P. - ASSOCIAZIONE ITALIANA EMATOLOGIA ONCOLOGIA PEDIATRICA | |||||||||||||
Full Title: INTERNATIONAL COLLABORATIVE TREATMENT PROTOCOL FOR INFANTS UNDER ONE YEAR WITH ACUTE LYMPHOBLASTIC OR BIPHENOTYPIC LEUKEMIA | |||||||||||||
Medical condition: acute lymphoblastic leukemia (ALL) or biphenotypic leukemia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) BE (Completed) FR (Ongoing) DE (Completed) GB (Completed) AT (Ongoing) PT (Completed) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
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