- Trials with a EudraCT protocol (66)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
66 result(s) found for: Noninferiority trial.
Displaying page 1 of 4.
EudraCT Number: 2009-013326-17 | Sponsor Protocol Number: MI-CP208 | Start Date*: 2013-05-20 |
Sponsor Name:MedImmune, LLC | ||
Full Title: A Randomized, Double-Blind, Active Controlled Study to Evaluate the Immunogenicity of Quadrivalent LAIV in Children | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-003655-15 | Sponsor Protocol Number: CA209-67T | Start Date*: 2021-06-02 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 3, Open-label, Randomized, Noninferiority Trial of Subcutaneous Formulation of Nivolumab Versus Intravenous Nivolumab in Participants With Advanced or Metastatic Clear Cell Renal Cell Carci... | |||||||||||||
Medical condition: Metastatic Clear Cell Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) PT (Trial now transitioned) FI (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005978-79 | Sponsor Protocol Number: KLF/K/01105 | Start Date*: 2007-07-05 |
Sponsor Name:MCM Klosterfrau GmbH | ||
Full Title: Proof of the noninferiority of a benzocain containing lozenge compared to Anaesthesin pastilles on patients with acute pharyngitis | ||
Medical condition: Acute Pharyngitis | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002370-39 | Sponsor Protocol Number: ALXN1210-PNH-303 | Start Date*: 2019-07-02 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Parallel-Group, Multicenter, Open-Label, Pharmacokinetic, Noninferiority Study of Ravulizumab Administered Subcutaneously Versus Intravenously in Adult Patients With Paroxys... | |||||||||||||
Medical condition: Paroxysmal Nocturnal Hemoglobinuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) NL (Ongoing) SE (Completed) FI (Completed) CZ (Completed) ES (Ongoing) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000505-72 | Sponsor Protocol Number: 2019-000505-72 | Start Date*: 2019-05-13 |
Sponsor Name:Transparency in Healthcare | ||
Full Title: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Medical condition: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004167-29 | Sponsor Protocol Number: NA | Start Date*: 2021-03-15 |
Sponsor Name:CHU de Liège | ||
Full Title: Study of the noninferiority of an oral versus intravenous administration of tranexamic acid in total hip arthroplasty | ||
Medical condition: Bleeding in total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002467-26 | Sponsor Protocol Number: 480-SFA2013-001 | Start Date*: 2013-08-30 |
Sponsor Name:480 Biomedical, Inc. | ||
Full Title: The SPRINT trial: An Evaluation of the 480 Biomedical STANZA™ Drug-Eluting Resorbable Scaffold (DRS) System v1.2 in the Treatment of de novo SFA Lesions | ||
Medical condition: An evaluation of the safety and performance of the STANZA DRS v1.2 system for the treatment of patients with obstructive superficial femoral artery disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024129-20 | Sponsor Protocol Number: ProyectoOB12 | Start Date*: 2011-06-07 | |||||||||||
Sponsor Name:Consorcio de Apoyo a la Investigación Biomédica en red (CAIBER) | |||||||||||||
Full Title: Oral Versus Intramuscular Cobalamin to treat Cobalamin Deficiency: Noninferiority randomised controlled trial, pragmatic and multi-center in the primary healthcare setting (OB12 project). | |||||||||||||
Medical condition: Vitamin B12 (cianocobalamin) defficiency | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003686-18 | Sponsor Protocol Number: GESIDA11720 | Start Date*: 2021-04-29 |
Sponsor Name:Seimc-Gesida Foundation | ||
Full Title: DTG/3TC vs. BIC/FTC/TAF maintenance therapy in people living with HIV: an open-label randomized clinical trial | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004893-14 | Sponsor Protocol Number: ASR115645 | Start Date*: 2016-08-03 |
Sponsor Name:GlaxoSmithKline Research & Development | ||
Full Title: A Randomised, Multi-centre, Double-blind, Double-dummy, two way cross-over, twelve weeks noninferiority study to evaluate the efficacy, safety and tolerability of combination dry powder Fluticasone... | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-011497-15 | Sponsor Protocol Number: CERA | Start Date*: 2009-05-07 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: PILOT CLINICAL TRIAL WITH MIRCERA (methoxy polyethylene glycol-epoetin beta) IN DIALYSIS UNIT OF A.O. SAN GIOVANNI BATTISTA DI TORINO | |||||||||||||
Medical condition: End stage renal patients in hemodialysis or peritoneal dialysis treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005891-21 | Sponsor Protocol Number: I8H-MC-BDCX | Start Date*: 2022-08-04 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Parallel-Design, Open-Label, Randomized Control Study to Evaluate the Efficacy and Safety of LY3209590 as a Weekly Basal Insulin Compared to Insulin Degludec in Insulin Naïve Adults with... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003675-35 | Sponsor Protocol Number: WV2018 | Start Date*: 2018-11-01 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Efficacy of Very Early Medical Abortion – a randomized controlled non-inferiority trial | ||
Medical condition: Unwanted pregnancy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) FI (Completed) AT (Ongoing) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002756-91 | Sponsor Protocol Number: LPS14947 | Start Date*: 2019-10-24 | |||||||||||
Sponsor Name:Sanofi Aventis Groupe | |||||||||||||
Full Title: A 12-week randomized, controlled trial to compare TOUJEO® and TRESIBA® in terms of glucose values in target range and variability during continuous glucose monitoring in patients with type 1 diabet... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017814-56 | Sponsor Protocol Number: NN5401-3599 | Start Date*: 2011-01-31 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 26-week, randomised, open-label, multinational, treat-to-target trial comparing efficacy and safety of insulin degludec/insulin aspart once daily (OD) and insulin glargine OD both in combination ... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005499-20 | Sponsor Protocol Number: RM21 | Start Date*: 2022-07-05 |
Sponsor Name:Research Maatschap Cardiologen Rotterdam Zuid | ||
Full Title: COMPARE STEMI ONE- Comparison Of reduced DAPT followed by P2Y12 inhibitor Monotherapy with Prasugrel vs stAndard Regimen in STEMI patients treated with OCT-guided vs aNgio-guided completE revascul... | ||
Medical condition: ST elevated myocard infarction followed by PCI | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002381-23 | Sponsor Protocol Number: LOCAL/2012/PGC-01 | Start Date*: 2015-10-16 |
Sponsor Name:CHU de Nîmes | ||
Full Title: Comparison of the efficacy of IV paracetamol and IV ketoprofen in the treatment of renal colic in emergency department : a two-center double blind randomized study. | ||
Medical condition: Comparison of the efficacy of IV paracetamol and IV ketoprofen in the treatment of renal colic | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003768-19 | Sponsor Protocol Number: CSLCT-USF-07-36 | Start Date*: 2015-01-08 |
Sponsor Name:CSL Limited | ||
Full Title: A Phase III, Randomized, Observer-blind, Multi-center, Noninferiority Comparison of the Immune Response of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Trivalent Inactivated Spli... | ||
Medical condition: Influenza, human | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-002785-13 | Sponsor Protocol Number: V130_10 | Start Date*: 2020-12-04 | |||||||||||
Sponsor Name:Seqirus Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Observer-Blind, Multicenter, Noninferiority Study to Evaluate Safety and Immunogenicity of a Cell-Based Quadrivalent Subunit Influenza Virus Vaccine (QIVc) and a United State... | |||||||||||||
Medical condition: Prophylaxis of Influenza Virus Infection | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014803-30 | Sponsor Protocol Number: H9X-MC-GBDB | Start Date*: 2010-06-09 | |||||||||||
Sponsor Name:Lilly S.A. | |||||||||||||
Full Title: Estudio abierto, aleatorizado, con dos ramas paralelas, comparativo de no inferioridad de los efectos de dos dosis de LY2189265 versus insulina glargina sobre el control glucémico en pacientes con ... | |||||||||||||
Medical condition: Diabetes Mellitus tipo 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) FR (Completed) HU (Completed) SK (Completed) CZ (Completed) BE (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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