- Trials with a EudraCT protocol (518)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
518 result(s) found for: Phenotype.
Displaying page 1 of 26.
EudraCT Number: 2022-000404-35 | Sponsor Protocol Number: 80519 | Start Date*: 2022-07-26 |
Sponsor Name:AMC, Cardiovascular Sciences | ||
Full Title: Does the hematopoietic stem cell govern residual inflammatory cardiovascular risk in type 2 diabetes? | ||
Medical condition: Inflammation in patients with type 2 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001285-11 | Sponsor Protocol Number: P20.XXX | Start Date*: 2021-01-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A Randomized, open label, Non-inferiority trial on the efficacy of Lacosamide versus Duloxetine in Patients with Chemotherapy-induced Polyneuropathy – A strategy trial | ||
Medical condition: Chemotherapy-induced polyneuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002037-31 | Sponsor Protocol Number: 2017/15 | Start Date*: 2020-01-07 | |||||||||||
Sponsor Name:Centre Antoine-LACASSAGNE | |||||||||||||
Full Title: Study of the impact of DPD activity on the efficacy of capecitabine | |||||||||||||
Medical condition: Metastatic HER2-negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019380-11 | Sponsor Protocol Number: 09/0278 | Start Date*: 2010-09-30 |
Sponsor Name: | ||
Full Title: Autologous cell therapy of fracture non-union – cell phenotype as a predictor of outcome | ||
Medical condition: delayed fracture union (fracture non-union) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023331-42 | Sponsor Protocol Number: IMIOXC | Start Date*: 2010-12-15 | |||||||||||
Sponsor Name:Department of Neurology, Odense University Hospital | |||||||||||||
Full Title: Oxcarbazepine for the treatment of chronic peripheral neuropathic pain: predictors of response - a randomised, double-blind, placebo-controlled clinical trial | |||||||||||||
Medical condition: Chronic peripheral neuropathic pain caused by polyneuropathy, postherpetic neuralgia and traumatic/surgical nerve injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000178-20 | Sponsor Protocol Number: MCT8-2014-1 | Start Date*: 2015-08-12 |
Sponsor Name:Erasmus Medical Centre | ||
Full Title: Thyroid hormone analog therapy of patients with severe psychomotor retardation caused by mutations in the MCT8 thyroid hormone transporter: The Triac Trial. | ||
Medical condition: This therapuetical trial will be conducted in patient with the Allan-Herndon-Dudley Syndrome (AHDS), casued by mutations in the thyroid hormone transporter MCT8. This results in the characteristic ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male | |
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) IT (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003110-40 | Sponsor Protocol Number: LACOSAMIDE-2018 | Start Date*: 2018-09-11 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: The effect of lacosamide in peripheral neuropathic pain: a randomized, double-blind, placebo-controlled, phenotype-stratified study | |||||||||||||
Medical condition: Peripheral Neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001866-15 | Sponsor Protocol Number: 1182.71 | Start Date*: 2007-07-12 |
Sponsor Name:Boehringer Ingelheim France SAS | ||
Full Title: A prospective randomized, open-labelled, multi-centre trial comparing the safety and efficacy of Ritonavir-boosted Aptivus (Tipranavir, TPV/r) to that of Prezista® (Darunavir, DRV/r) in three-clas... | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) ES (Completed) DE (Prematurely Ended) GR (Completed) PT (Prematurely Ended) IT (Prematurely Ended) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001393-34 | Sponsor Protocol Number: MNILCAPS001 | Start Date*: 2014-04-14 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Ilaris® (canakinumab) efficacy and safety in CAPS patients without confirmed mutation on exon 3 of gene CIAS1 and young (<2yrs) CAPS patients with severe neurological (CINCA) phenotype. | |||||||||||||
Medical condition: Cryopyrin-Associated Periodic Syndromes | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003612-28 | Sponsor Protocol Number: 206785 | Start Date*: 2021-06-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 52-week, randomised, double-blind, double-dummy, parallel group,multi-centre, non-inferiority study assessing exacerbation rate, additional measures of asthma control and safety in adult and ad... | |||||||||||||
Medical condition: Severe asthma with an eosinophilic phenotype | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) SI (Trial now transitioned) NO (Trial now transitioned) PL (Completed) FI (Trial now transitioned) IT (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) IE (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003611-10 | Sponsor Protocol Number: 213744 | Start Date*: 2021-07-06 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 52-week, randomised, double-blind, placebo-controlled, parallel-group, multi-centre study of the efficacy and safety of GSK3511294 adjunctive therapy in adult and adolescent participants with sev... | |||||||||||||
Medical condition: Severe uncontrolled asthma with an eosinophilic phenotype | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) PL (Completed) IT (Completed) ES (Ongoing) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001298-17 | Sponsor Protocol Number: 362/11 | Start Date*: 2012-04-05 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Phase II study on ET-743 in BRCA1 and BRCA2 mutation carrie and BRCAness phenotype advanced ovarian cancer patients. | |||||||||||||
Medical condition: advaced ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000123-37 | Sponsor Protocol Number: CONCEPT-ACS | Start Date*: 2023-05-12 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Efficacy of CONservative versus invasive therapy in acute Coronary syndrome with plaque Erosion PhenoType - the CONCEPT-ACS trial | |||||||||||||
Medical condition: patients affected by acute coronary syndrome with plaque erosion phenotype | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000836-24 | Sponsor Protocol Number: IIV-406 | Start Date*: 2019-06-19 |
Sponsor Name:National Institute of Health and the Environment | ||
Full Title: Immune responses to influenza and pneumococcal conjugate vaccines in older adults compared to middle-aged adults and adults. | ||
Medical condition: Healthy volunteers above 25 years of age | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006652-19 | Sponsor Protocol Number: NILG-ALL 10/07 | Start Date*: 2008-02-06 | |||||||||||
Sponsor Name:NILG | |||||||||||||
Full Title: A Randomized Pilot Study on Central Nervous System (CNS) Prophylaxis with Liposome-Encapsulated Cytarabine (DepoCyte) in a Population of Adult Patients with Acute Lymphoblastic Leukemia (ALL) Treat... | |||||||||||||
Medical condition: 2. Diagnosis of untreated ALL with B-/T-precursor phenotype or B/T-LL, either de novo or secondary to chemo-radiotherapy for other cancer. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004905-15 | Sponsor Protocol Number: 2013103120 | Start Date*: 2014-01-22 | |||||||||||
Sponsor Name:Respiratory Research Unit, Bispebjerg Hospital | |||||||||||||
Full Title: Does asthma phenotype have impact on disease control | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003077-26 | Sponsor Protocol Number: IMIVER | Start Date*: 2012-08-13 | |||||||||||
Sponsor Name:Department of Neurology, Odense University Hospital | |||||||||||||
Full Title: Topical lidocaine for the treatment of focal peripheral neuropathic pain: response in relation to pain phenotype | |||||||||||||
Medical condition: Chronic peripheral neuropathic pain caused by postherpetic neuralgia and traumatic/surgical nerve injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004419-35 | Sponsor Protocol Number: GN13RH410 | Start Date*: 2015-03-18 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Inhibition of Co-Stimulation in Rheumatoid Arthritis | |||||||||||||
Medical condition: Rheumatoid Arthritis: patients who are dual ACPA and HLA-DR4 positive | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002578-29 | Sponsor Protocol Number: 2019-5787 | Start Date*: 2020-01-21 |
Sponsor Name:Radboudumc | ||
Full Title: Functional Improvement of non-infarcT relaTed coronary artery stenosis by Extensive LDL-C Reduction with a PCSK9 Antibody. | ||
Medical condition: Coronary artery disease (CAD) Optimal treatment approach for bystander lesions in non-infarct related arteries (non-IRA’s) has not been well established. Multiple RCT’s favor preventive PCI over ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004472-30 | Sponsor Protocol Number: MITO23 | Start Date*: 2015-12-02 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Randomized phase III trial on Trabectedin (ET-743) vs clinician’s choice chemotherapy in recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
Medical condition: recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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