- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Nutrition transition.
Displaying page 1 of 1.
EudraCT Number: 2014-004078-40 | Sponsor Protocol Number: CQR14002 | Start Date*: 2015-01-28 | |||||||||||
Sponsor Name:CeQur Corp. | |||||||||||||
Full Title: A Prospective, Single Center, Observational Study to Assess the Performance, Safety, and Patient Reported Outcomes of Insulin Delivery with PaQ® in Patients with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003060-31 | Sponsor Protocol Number: HMPL-004-04 | Start Date*: 2014-02-17 | |||||||||||
Sponsor Name:Nutrition Science Partners Limited | |||||||||||||
Full Title: A Phase III Double Blind, Multi-Center Placebo Controlled Maintenance Trial of HMPL-004 in Subjects with Mild to Moderate Ulcerative Colitis with Clinical Remission or Response from Induction Thera... | |||||||||||||
Medical condition: Ulcerative Colitis (UC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000452-34 | Sponsor Protocol Number: 3004 | Start Date*: 2013-11-19 | |||||||||||
Sponsor Name:Steno Diabetes Center | |||||||||||||
Full Title: Proteomic prediction and Renin angiotensin aldosterone system Inhibition prevention Of early diabetic nephRopathy In TYpe 2 diabetic patients with normoalbuminuria | |||||||||||||
Medical condition: Patients with type 2 diabetes mellitus and normoalbuminuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) IT (Completed) GB (Completed) NL (Completed) ES (Completed) CZ (Completed) GR (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004712-10 | Sponsor Protocol Number: PT003014 | Start Date*: 2015-08-06 | ||||||||||||||||
Sponsor Name:Pearl Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double Blind, Chronic Dosing (24 Weeks), Placebo Controlled, Parallel Group, Multi-Center Study to Assess the Efficacy and Safety of PT003, PT005, and PT001 in Subjects with Moderate ... | ||||||||||||||||||
Medical condition: Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) PL (Completed) HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001832-39 | Sponsor Protocol Number: LPS14060 | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:sanofi-aventis Groupe | |||||||||||||
Full Title: A twenty-six week, randomized, open-label, 2-arm parallel group real world pragmatic trial to assess the clinical and health outcomes benefit of transition to Toujeo compared to standard of care in... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) FI (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006322-25 | Sponsor Protocol Number: SPD602-301 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Shire Development LLC | |||||||||||||
Full Title: A Phase 2, Open-label, Multicentre, Extension Safety and Tolerability Study for Transfusionally Iron Overloaded Children, Adolescents and Adults Using SSP-004184 (SPD602). | |||||||||||||
Medical condition: Patients with transfusional iron overload due to hereditary anemias such as sickle cell disease, beta-thalassemia and Diamond-Blackfan anemia; aquired anemias such as Myelodysplastic Syndrome and o... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015386-30 | Sponsor Protocol Number: GLP108486 | Start Date*: 2010-01-29 | |||||||||||
Sponsor Name:GlaxoSmithKline LLC | |||||||||||||
Full Title: A Randomized, Open-Label, Active-Controlled, Parallel-Group, Multicenter Study to Determine the Safety and Efficacy of Albiglutide Administered in Combination With Insulin Glargine as Compared with... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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