- Trials with a EudraCT protocol (1,103)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,103 result(s) found for: Nutritional and Metabolic Diseases.
Displaying page 26 of 56.
EudraCT Number: 2019-000398-21 | Sponsor Protocol Number: NLY01-D1 | Start Date*: 2019-08-26 | |||||||||||
Sponsor Name:Neuraly, Inc. | |||||||||||||
Full Title: A Phase 2a Dose-Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of NLY01, a PEGylated Exenatide, when Administered as a Single Dose in Subjects with Type 2 D... | |||||||||||||
Medical condition: Type 2 Diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000146-18 | Sponsor Protocol Number: TM008 | Start Date*: 2022-02-09 | |||||||||||
Sponsor Name:Saniona A/S | |||||||||||||
Full Title: A Phase 2b, Double-blind, Randomized, Placebo-controlled, Dose finding, Multi-center, 36-week Safety and Efficacy Study with Open-label Extension Period of Tesomet in Subjects with Hypothalamic Obe... | |||||||||||||
Medical condition: Hypothalamic Obesity | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003313-28 | Sponsor Protocol Number: CRC-KliPha-001 | Start Date*: 2015-10-26 | |||||||||||
Sponsor Name:Hannover Medical School | |||||||||||||
Full Title: SGLT2 inhibition with empagliflozin in patients with type 2 diabetes mellitus: Influences on left ventricular mass, function, and cardiac lipid content (EMPATROPHY) | |||||||||||||
Medical condition: Patients with type 2 diabetes mellitus on background metformin treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001155-40 | Sponsor Protocol Number: 16032020 | Start Date*: 2020-08-20 | ||||||||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | ||||||||||||||||||
Full Title: Kidney Fat in Type 2 Diabetes & Diabetic Kidney Disease and the Effects of Ezetimibe: A Cross-Sectional Study and Randomized, Placebo-Controlled Trial | ||||||||||||||||||
Medical condition: Type 2 diabetes, diabetic kidney disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003339-53 | Sponsor Protocol Number: I8H-MC-BDCL | Start Date*: 2020-09-22 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2, Parallel, Comparator-Controlled Trial to Evaluate the Safety and Efficacy of LY3209590 in Insulin-Naïve Patients with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000321-31 | Sponsor Protocol Number: rhLAMAN-09 | Start Date*: 2013-06-07 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A multi-center, un-controlled, open-labeled trial of the long-term safety of Velmanase Alfa aftercare treatment of subjects with alpha-Mannosidosis whom previously participated in Velmanase Alfa - ... | |||||||||||||
Medical condition: Treatement of Alpha-Mannosidosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000444-58 | Sponsor Protocol Number: CT041-ADO09 | Start Date*: 2021-02-12 | |||||||||||
Sponsor Name:Adocia | |||||||||||||
Full Title: A Phase 2 Trial to Assess the Efficacy and Safety of M1 Pram P037 prandial insulin in T1DM subjects | |||||||||||||
Medical condition: Type 1 diabetes mellitus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001897-27 | Sponsor Protocol Number: GC41033 | Start Date*: 2020-01-07 | |||||||||||
Sponsor Name:Genentech Inc | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, PARALLEL-GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TOEVALUATE THE EFFICACY, SAFETY, AND PHARMACOKINETICS OF BFKB8488A COMPAREDWITH PLACEBO IN PATIENTS WITH ... | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis (NASH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005643-26 | Sponsor Protocol Number: PrefoCir2 | Start Date*: 2012-03-15 | ||||||||||||||||
Sponsor Name:ZAMBON ITALIA | ||||||||||||||||||
Full Title: Cross-over pharmacokinetic study and pharmacodynamics of 2 different folate (5-MTHF and folic acid) in patients with liver cirrhosis with viral etiology. A randomized, open-label trial. | ||||||||||||||||||
Medical condition: In all cases of folate deficiency due to increased demand, poor absorption, inadequate dietary intake and reduced utilization of the vitamin in patients with viral liver cirrhosis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001046-17 | Sponsor Protocol Number: SMART-2019 | Start Date*: 2019-05-02 | |||||||||||
Sponsor Name:Uppsala University | |||||||||||||
Full Title: A multicentre, register-based, randomized, controlled trial comparing dapagliflozin with metformin treatment in early stage type 2 diabetes patients by assessing mortality and macro- and microvascu... | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001158-23 | Sponsor Protocol Number: U1111-1243-4058 | Start Date*: 2023-06-01 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Fast-Acting Insulin Aspart and Insulin Pump Settings: “THE FAST PUMP SETTING STUDY” | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003611-62 | Sponsor Protocol Number: LIB003-003 | Start Date*: 2020-03-20 | |||||||||||
Sponsor Name:LIB Therapeutics, LLC | |||||||||||||
Full Title: Randomized, Open-Label, Cross-Over, Phase 3 Study to Evaluate the Efficacy and Safety of LIB003 with Evolocumab in Homozygous Familial Hypercholesterolemia Patients on Stable Lipid-Lowering Therapy. | |||||||||||||
Medical condition: Homozygous Familial Hypercholesterolemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000033-33 | Sponsor Protocol Number: 83631 | Start Date*: 2023-05-03 | |||||||||||||||||||||
Sponsor Name:Maastricht University | |||||||||||||||||||||||
Full Title: Short-term safety and efficacy of ketohexokinase inhibition in patients with hereditary fructose intolerance. | |||||||||||||||||||||||
Medical condition: Hereditary fructose intolerance | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004663-12 | Sponsor Protocol Number: PAOFIN2017 | Start Date*: 2019-05-08 | |||||||||||
Sponsor Name:A.O.U. Università degli Studi della Campania "Luigi Vanvitelli" | |||||||||||||
Full Title: Geriatric outcomes among older Type 2 diabetic patients treated with DPP4 inhibitors or glinides: focus on cognitive functioning (GOOD-WP3) | |||||||||||||
Medical condition: type 2 diabetes mellitus | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003126-16 | Sponsor Protocol Number: CANA-1 | Start Date*: 2016-10-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | |||||||||||||
Full Title: A PHASE II, RANDOMIZED, CROSS-OVER, DOUBLE-BLIND, PLACEBO-CONTROLLED, SINGLE CENTER STUDY OF THE EFFECT OF THE ACUTE ADMINISTRATION OF THE SGLT-2 INHIBITOR CANAGLIFLOZIN ON CONTERREGULATORY RESPONS... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005140-41 | Sponsor Protocol Number: Saxa-Dapa1 | Start Date*: 2017-05-10 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | ||||||||||||||||||
Full Title: A PHASE II, RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED, PARALLEL-GROUP, SINGLE CENTER PILOT STUDY OF THE ACUTE AND CHRONIC EFFECTS OF DAPAGLIFLOZIN PLUS SAXAGLIPTIN IN ADDITION TO METFORMIN VERSUS... | ||||||||||||||||||
Medical condition: Patients with type 2 diabetes poorly controlled with metformin | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002031-29 | Sponsor Protocol Number: R7257-RAA-1947 | Start Date*: 2020-11-05 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 1/2 STUDY OF REGN7257 (ANTI-INTERLEUKIN 2 RECEPTOR SUBUNIT GAMMA [IL2RG] MONOCLONAL ANTIBODY) IN PATIENTS WITH SEVERE APLASTIC ANEMIA THAT IS REFRACTORY TO OR RELAPSED ON IMMUNOSUPPRESSIVE ... | |||||||||||||
Medical condition: SEVERE APLASTIC ANEMIA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001303-36 | Sponsor Protocol Number: TRCA-303 | Start Date*: 2018-11-07 | |||||||||||
Sponsor Name:Tricida Inc. | |||||||||||||
Full Title: A Phase 3b, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of TRC101 in Delaying Chronic Kidney Disease Progression in Subjects with Metabolic Acidosis | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Prematurely Ended) GB (GB - no longer in EU/EEA) FR (Completed) SK (Completed) CZ (Completed) BE (Completed) ES (Prematurely Ended) PT (Completed) NL (Prematurely Ended) PL (Completed) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003164-21 | Sponsor Protocol Number: 652-2-203 | Start Date*: 2015-01-05 | |||||||||||
Sponsor Name:Tobira Therapeutics, Inc., a subsidiary of Allergan plc | |||||||||||||
Full Title: Efficacy and Safety Study of Cenicriviroc for the Treatment of Nonalcoholic Steatohepatitis (NASH) in Adult Subjects with Liver Fibrosis | |||||||||||||
Medical condition: Nonalcoholic Steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) IT (Completed) DE (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000963-22 | Sponsor Protocol Number: VTX-801_CLN_001 | Start Date*: 2021-10-18 | |||||||||||
Sponsor Name:Vivet Therapeutics SAS | |||||||||||||
Full Title: A Phase I/II, Multicenter, Non-randomized, Open Label, Adaptive Design, 5-year Follow-up, Single Dose-escalation Study of VTX-801 in Adult Patients with Wilson’s Disease | |||||||||||||
Medical condition: Wilson's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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