- Trials with a EudraCT protocol (2,506)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,506 result(s) found for: Tubal ligation.
Displaying page 8 of 126.
EudraCT Number: 2006-001138-42 | Sponsor Protocol Number: CLAF237A23103 | Start Date*: 2006-08-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group Study to Compare the Effect of 24 Weeks Treatment with Vildagliptin 100 mg qd to Placebo as Add-On Therapy in Patients with Type 2 Diabetes I... | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003073-27 | Sponsor Protocol Number: RD.03.SPR29064 | Start Date*: 2007-02-06 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject preference comparison between Clobetasol propionate shampoo, 0.05% and three other topical corticosteroids in the treatment of moderate to severe Scalp psoriasis | |||||||||||||
Medical condition: Moderate to Severe Scalp Psoriasis with a Global Severity Score of 3 at least on a scale from 0 to 5. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003242-22 | Sponsor Protocol Number: BCX4161-303 | Start Date*: 2015-12-17 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: OPuS-4: An open-label study to evaluate the long-term safety of avoralstat in subjects with hereditary angioedema | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) HU (Prematurely Ended) BE (Completed) FR (Prematurely Ended) GB (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012188-32 | Sponsor Protocol Number: 113094 | Start Date*: 2009-09-17 |
Sponsor Name:GlaxosmithKline Biologicals | ||
Full Title: A phase III, observer-blind, multicountry, multicentre study to evaluate the safety, reactogenicity and immunogenicity of GlaxoSmithKline Biologicals’ GSK2186877A influenza vaccine administered to ... | ||
Medical condition: Immunization against influenza in male and female subjects aged 19-43 years and 66 years or older. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) SE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004571-41 | Sponsor Protocol Number: RBMinCovid19 | Start Date*: 2021-02-23 | |||||||||||
Sponsor Name:Cyxone AB | |||||||||||||
Full Title: A Randomized, Placebo Controlled, Double Blind Study to Evaluate the Safety and Efficacy of Rabeximod Compared to Standard of Care in Patients With Moderate Coronavirus Disease (COVID-19) | |||||||||||||
Medical condition: Coronavirus Disease (COVID-19) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Prematurely Ended) LV (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002690-19 | Sponsor Protocol Number: D9150C00003 | Start Date*: 2017-12-14 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A randomized, double-blind, placebo-controlled, multi-centre, sequential design, phase IIa study to evaluate safety and tolerability of epicardial injections of AZD8601 during coronary bypass graf... | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) NL (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001863-21 | Sponsor Protocol Number: FIOL | Start Date*: 2018-08-14 |
Sponsor Name:Vestre Viken Hospital Trust | ||
Full Title: First-line treatment with osimertinib in EGFR-mutated non-small cell lung cancer, coupled to extensive translational studies. | ||
Medical condition: Lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) LT (Trial now transitioned) DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002140-10 | Sponsor Protocol Number: N01125 | Start Date*: 2005-08-24 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: An open-label, multi-center, follow-up trial to evaluate long-term safety and efficacy of brivaracetam (ucb 34714) used as adjunctive treatment at a flexible dose up to a maximum of 200 mg/day in s... | |||||||||||||
Medical condition: Epilepsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) GB (Completed) FI (Completed) ES (Completed) IT (Completed) SE (Completed) HU (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002168-17 | Sponsor Protocol Number: BAY94-8862/16275 | Start Date*: 2015-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, double-dummy, parallel-group, active-controlled study to evaluate the efficacy and safety of finerenone compared to eplerenone on morbidity and mortality in... | |||||||||||||||||||||||||||||||||
Medical condition: Subjects with chronic heart failure and reduced ejection fraction after recent heart failure decompensation and additional risk factors, either type 2 diabetes mellitus or chronic kidney disease or... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) LT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002708-25 | Sponsor Protocol Number: RIVAROXACS3001 (BAY59-7939/13194) | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Event-Driven Multicenter Study to Evaluate the Efficacy and Safety of Rivaroxaban in Subjects with a Recent Acute Coronary Syndrome The ATLAS ACS 2 ... | |||||||||||||
Medical condition: Acute Coronary Syndrome (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) LT (Completed) DE (Completed) PT (Completed) SK (Completed) HU (Completed) FR (Completed) DK (Completed) GB (Completed) NL (Completed) ES (Completed) IT (Completed) LV (Completed) CZ (Completed) BG (Completed) BE (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011222-34 | Sponsor Protocol Number: SYR-322_402 | Start Date*: 2009-11-09 | ||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Cardiovascular Outcomes Following Treatment with Alogliptin in Addition to Standard of Care in Subjects with Type 2 Di... | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) and acute coronary syndrome (ACS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) HU (Completed) ES (Completed) CZ (Completed) SE (Completed) DE (Completed) FR (Completed) DK (Completed) IT (Completed) BG (Completed) LV (Completed) FI (Completed) LT (Completed) AT (Completed) SK (Completed) PT (Completed) GB (Completed) GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004066-10 | Sponsor Protocol Number: MVT-601-3103 | Start Date*: 2018-10-19 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: SPIRIT EXTENSION: An International Phase 3 Open-Label, Single-Arm, Safety and Efficacy Extension Study to Evaluate Relugolix Co-Administered with Low-Dose Estradiol and Norethindrone Acetate in Wom... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) BE (Completed) FI (Completed) SE (Completed) PL (Completed) CZ (Completed) BG (Completed) PT (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002101-21 | Sponsor Protocol Number: ARGX-113-1803 | Start Date*: 2020-05-25 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-label, Long-term Trial to Evaluate the Safety and Efficacy of Efgartigimod (ARGX-113) 10 mg/kg Intravenous in Adult Patients With Primary Immune Thrombocytopenia | |||||||||||||
Medical condition: Primary immune thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Completed) HU (Trial now transitioned) FR (Completed) BE (Completed) CZ (Trial now transitioned) BG (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003351-65 | Sponsor Protocol Number: RDD110 | Start Date*: 2016-03-16 |
Sponsor Name:RDD Pharma Ltd. | ||
Full Title: The Effect of Intra-anal Nifedipine, Used As Add-on to Conservative Therapy, on Pain in Patients with Anal Fissure | ||
Medical condition: Anal Fissure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BG (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002316-51 | Sponsor Protocol Number: 02PDE2019 | Start Date*: 2020-09-25 |
Sponsor Name:Celon Pharma SA | ||
Full Title: Phase II, Double blind, Randomized, Placebo Controlled, Parallel Group, Trial to Explore Efficacy, Safety and Pharmacokinetics of CPL500036 (PDE10A inhibitor) in Patients with an Acute Exacerbation... | ||
Medical condition: Acute exacerbation of schizophrenia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Completed) HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000064-21 | Sponsor Protocol Number: TPN-101-AGS-201 | Start Date*: 2022-09-20 | |||||||||||
Sponsor Name:Transposon Therapeutics Inc | |||||||||||||
Full Title: A Phase 2a Study of TPN-101 in Patients with Aicardi-Goutières Syndrome (AGS) | |||||||||||||
Medical condition: Aicardi-Goutières Syndrome (AGS) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001890-98 | Sponsor Protocol Number: HPV001 | Start Date*: 2020-05-29 | |||||||||||
Sponsor Name:Vaccitech Ltd. | |||||||||||||
Full Title: A Phase 1b/2 Randomised, Placebo-controlled, Dose-ranging Study to Evaluate Safety, Tolerability and Immunogenicity of a Chimpanzee Adenovirus (ChAdOx1)-vectored Multigenotype High Risk Human Papil... | |||||||||||||
Medical condition: Persistent hrHPV infection in participants with low grade cervical lesions | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001178-20 | Sponsor Protocol Number: IM103-307,SMR-2729 | Start Date*: 2013-10-29 | |||||||||||
Sponsor Name:Uppsala University Hospital, MHT, Department of Nephrology | |||||||||||||
Full Title: Cardiovascular (CV) risk prediction and CV biomarkers in renal transplant recipients treated with belatacept compared to calcineurin inhibitors (CNI). Open randomized 12 month study. | |||||||||||||
Medical condition: Prophylaxis of graft rejection in adults who have received a renal transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002052-27 | Sponsor Protocol Number: DRM04-HH04 | Start Date*: 2015-10-14 | |||||||||||
Sponsor Name:Dermira, Inc. | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, VEHICLE-CONTROLLED EFFICACY AND SAFETY STUDY OF DRM04 IN SUBJECTS WITH AXILLARY HYPERHIDROSIS | |||||||||||||
Medical condition: Primary axillary hyperhidrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002532-24 | Sponsor Protocol Number: 0155/2018 | Start Date*: 2018-12-27 | |||||||||||
Sponsor Name:HELM AG | |||||||||||||
Full Title: A phase III, multicentre, randomised, double-blind, parallel-group trial to evaluate the efficacy and safety of a generic gel (calcipotriol + betamethasone 50 μg/g + 0.5 mg/g gel) compared to origi... | |||||||||||||
Medical condition: mild to moderate plaque-type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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