- Trials with a EudraCT protocol (1,169)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,169 result(s) found for: Levels of biomarkers.
Displaying page 8 of 59.
EudraCT Number: 2014-003532-39 | Sponsor Protocol Number: SitaBAT01 | Start Date*: 2014-11-24 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of sitagliptin on brown adipose tissue and whole-body metabolism in overweight pre-diabetic men | ||
Medical condition: Obesity, dyslipidemia and impaired glucose tolerance | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-004078-53 | Sponsor Protocol Number: 83403 | Start Date*: 2023-08-22 |
Sponsor Name:Academic Medical Center (AMC), department of Internal Medicine | ||
Full Title: Specifying the anti-inflammatory effects of ziltivekimab with diverse imaging modalities and in-depth cellular phenotyping | ||
Medical condition: - Plaque characteristics - Systemic inflammation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003829-29 | Sponsor Protocol Number: EMR200637-002 | Start Date*: 2014-10-27 | |||||||||||
Sponsor Name:Symphogen A/S | |||||||||||||
Full Title: Open-label, Randomized, Controlled, Multicenter Phase II Trial Investigating 2 Sym004 Doses versus Investigator`s Choice (Best Supportive Care, Capecitabine, 5-FU) in Subjects with Metastatic Color... | |||||||||||||
Medical condition: Metastatic colorectal cancer with Acquired Resistance to Anti-EGFR Monoclonal Antibodies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) BE (Completed) AT (Completed) HU (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004449-18 | Sponsor Protocol Number: HEP201 | Start Date*: 2019-04-10 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Promethera Biosciences | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Multicenter, open-label, safety and tolerability study of ascending doses of HepaStem in patients with cirrhotic and pre-cirrhotic non-alcoholic steatohepatitis (NASH). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: NASH is characterized by steatosis, inflammation and cytological ballooning with varying amounts of fibrosis. Patients with NASH are at risk of cardiovascular morbidity and mortality. In chronic li... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) BG (Completed) PL (Completed) ES (Ongoing) RO (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005755-20 | Sponsor Protocol Number: ALZ-801-AD301 | Start Date*: 2021-06-21 | |||||||||||
Sponsor Name:Alzheon, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-Controlled Study of the Efficacy, Safety and Biomarker Effects of ALZ-801 in Subjects with Early Alzheimer's Disease and APOE4/4 Genotype | |||||||||||||
Medical condition: Early Alzheimer’s Disease (AD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) NL (Completed) ES (Completed) CZ (Completed) IS (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023034-23 | Sponsor Protocol Number: B0151003 | Start Date*: 2011-06-03 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, DOSE-RANGING STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PF-04236921 IN SUBJECTS WITH CROHN’S DISEASE WHO ARE ANTI-TNF INADEQUATE RESPONDERS (ANDANTE) | |||||||||||||
Medical condition: Crohn's Disease (active moderate to severe) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) HU (Completed) GB (Completed) GR (Completed) DK (Completed) DE (Completed) BE (Completed) IT (Completed) CZ (Completed) AT (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005017-45 | Sponsor Protocol Number: NI-0101-04 | Start Date*: 2017-05-12 | |||||||||||
Sponsor Name:NovImmune S.A. | |||||||||||||
Full Title: A Randomized, Placebo-Controlled, Double Blind, Multicenter Phase 2 Study to Explore Tolerability, Safety, Pharmacokinetics, Pharmacodynamics and Efficacy of Intravenous Multiple Infusions of NI-01... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003826-10 | Sponsor Protocol Number: EAGLE | Start Date*: 2014-01-24 |
Sponsor Name:IRCCS- Mario Negri Institute | ||
Full Title: EVALUATING THE MORPHOFUNCTIONAL EFFECTS OF ECULIZUMAB THERAPY IN PRIMARY MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS: A PILOT, SINGLE ARM STUDY IN TEN PATIENTS WITH PERSISTENT HEAVY PROTEINURIA | ||
Medical condition: Membranoproliferative glomerulonephritis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005050-35 | Sponsor Protocol Number: 30102012 | Start Date*: 2014-12-01 | ||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
Full Title: Phase Ib/II study of metformin in combination with carboplatin/paclitaxel chemotherapy in patients with advanced ovarian cancer | ||||||||||||||||||
Medical condition: advanced ovarian cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002741-29 | Sponsor Protocol Number: CMAA868A2202 | Start Date*: 2018-05-15 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter, randomized, open-label, active-controlled, dose-range finding study to assess the pharmacodynamic parameters, safety and tolerability of MAA868 and its effect on thrombogenesis bioma... | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Suspended by CA) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003053-37 | Sponsor Protocol Number: 21952 | Start Date*: 2021-11-05 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A non-blinded retrospective biomarker add-on study to FIGARO-DKD for Bioprofiling the pharMacodynamic response to finerenone in FIGARO-DKD subjects (FIGARO-BM) | |||||||||||||
Medical condition: Type II Diabetes Mellitus and Diabetic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006226-49 | Sponsor Protocol Number: NN6019-4940 | Start Date*: 2022-08-18 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Efficacy and safety of NNC6019-0001 at two dose levels in participants with transthyretin amyloid cardiomyopathy (ATTR CM) | |||||||||||||
Medical condition: Transthyretin amyloid cardiomyopathy (ATTR CM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) PT (Trial now transitioned) DE (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003679-31 | Sponsor Protocol Number: 2015_22 | Start Date*: 2016-04-06 |
Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille | ||
Full Title: Conservative iron chelation as a disease-modifying strategy in Parkinson’s disease | ||
Medical condition: De Novo Parkinson’s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) ES (Ongoing) CZ (Completed) PT (Completed) FR (Completed) NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024213-31 | Sponsor Protocol Number: UNOLE0166 | Start Date*: 2012-09-12 | |||||||||||
Sponsor Name:University of Leicester | |||||||||||||
Full Title: Can Vitamin D Replacement Reduce Insulin resistance In South Asians with Vitamin D Deficiency? | |||||||||||||
Medical condition: Vitamin D Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003839-33 | Sponsor Protocol Number: UC-GMP/1908 | Start Date*: 2020-05-18 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: Phase II basket trial evaluating the efficacy of a combination of pembrolizumab and vorinostat in patients with recurrent and/or metastatic squamous cell carcinoma | |||||||||||||
Medical condition: Patients with recurrent and/or metastatic squamous cell carcinoma of the head and neck, cervix, lung, anal, vulva, and penile. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004458-14 | Sponsor Protocol Number: PROvING | Start Date*: 2020-11-05 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | ||||||||||||||||||||||||||||
Full Title: Phase III clinical trial Oligometastatic and Oligorecurrent PROstate Cancer: enhancing patients’ selection by new ImagiNG biomarkers | ||||||||||||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001172-15 | Sponsor Protocol Number: APN01-01-COVID19 | Start Date*: 2020-04-08 |
Sponsor Name:APEIRON Biologics AG | ||
Full Title: Recombinant human angiotensin-converting enzyme 2 (rhACE2) as a treat-ment for patients with COVID-19 | ||
Medical condition: Severe COVID-19 POSITIVE hospitalized male or female, between 18 and ≤ 80 years of age | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) DK (Completed) AT (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2015-002530-50 | Sponsor Protocol Number: EspeRare_RIM_001 | Start Date*: 2015-11-04 | |||||||||||
Sponsor Name:EspeRare | |||||||||||||
Full Title: A phase Ib, open label study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending oral doses of Rimeporide in patients with Duchenne Muscular Dystrophy. | |||||||||||||
Medical condition: Duchenne Muscular Dystrophy (DMD) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002473-19 | Sponsor Protocol Number: PNEU-ASTHMA-02 | Start Date*: 2018-11-13 |
Sponsor Name:Cliniques Universitaires Saint-Luc | ||
Full Title: PREDICTIVE FACTORS AND MAGNITUDE OF RESPONSE TO OMALIZUMAB AND MEPOLIZUMAB IN ALLERGIC AND EOSINOPHILIC SEVERE ASTHMA: A MULTICENTER PRAGMATIC TRIAL IN BELGIUM | ||
Medical condition: Adult patients (at least 18yrs-old) with severe asthma and eligible for both XOLAIR and NUCALA therapies, and agreeing on participating (signature of a written informed consent). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003775-35 | Sponsor Protocol Number: SHP655-201 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A Phase 2, multicenter, randomized, placebo-controlled, double-blind study in patients with acquired thrombotic thrombocytopenic purpura (aTTP) to evaluate the pharmacokinetics, safety, and efficac... | |||||||||||||
Medical condition: acquired thrombotic thrombocytopenic purpura (aTTP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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