- Trials with a EudraCT protocol (383)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
383 result(s) found for: Biological markers.
Displaying page 1 of 20.
EudraCT Number: 2008-006438-82 | Sponsor Protocol Number: 001 | Start Date*: 2009-06-15 |
Sponsor Name:Odense Universitetshospital, Nyremedicinsk Afd. Y | ||
Full Title: Vitamin D og kronisk nyreinsufficiens | ||
Medical condition: Investigating the effects of treatment with not activated vitamin D (cholecalciferol) in chronic kidney disease petients with vitamin D deficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-006113-34 | Sponsor Protocol Number: XAMNPIOAP2011 | Start Date*: 2013-10-24 |
Sponsor Name:AURORA PUJOL ONOFRE | ||
Full Title: Effect of pioglitazone administred to patients with Adrenomyeloneuropathy: A phase II, Singlearm, Monocentric Trial. | ||
Medical condition: X-linked adrenoleukodystrophy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001712-31 | Sponsor Protocol Number: | Start Date*: 2005-01-24 |
Sponsor Name:Lothian Health - University Hospitals Division | ||
Full Title: A study to evaluate the biological effects of RAD001 on invasive breast cancer | ||
Medical condition: Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004255-36 | Sponsor Protocol Number: Cesar | Start Date*: 2020-10-05 |
Sponsor Name:Karolinska Universitetssjukhuset | ||
Full Title: Cesar - an open, randomized controlled phase II study, comparing Naltrexon and Fluoxetin treating Compulsive Sexual Behavior Disorder. | ||
Medical condition: Compulsive Sexual Behavior Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002310-41 | Sponsor Protocol Number: “MADRID-COVID” | Start Date*: 2020-06-15 |
Sponsor Name:IIS FUNDACION JIMENEZ DIAZ | ||
Full Title: Intravenous Metoprolol in Respiratory Distress Due to COVID-19: Pilot Study "MADRID-COVID" | ||
Medical condition: The main objective of this pilot trial is to evaluate the effect of metoprolol on biological correlates of benefit of this therapy (inflammatory markers in blood and bronchoalveolar mini-lavage, mi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001952-32 | Sponsor Protocol Number: ACA-NETH-07-14 | Start Date*: 2008-11-07 |
Sponsor Name:Radboud University Nijmegen Medical Centre - Department of Dermatology | ||
Full Title: The effect of adalimumab on immune markers in lesional psoriatic skin. | ||
Medical condition: Plaque psoriasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005467-31 | Sponsor Protocol Number: 2020_843_0142 | Start Date*: 2021-01-28 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Effect of Tinzaparin on inflammatory biomarkers during the acute phase of deep vein thrombosis | ||
Medical condition: acute phase of deep vein thrombosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001174-33 | Sponsor Protocol Number: 28612 | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:Merck Serono International S.A., A branch of Laboratoires Serono S.A. | |||||||||||||
Full Title: A mulitnational, multicenter, exploratory pharmacogenomics trial to test the importance of identified genetic markers, and potentially identify new markers of various ovarian responses to GONAL-f® ... | |||||||||||||
Medical condition: Females undergoing assisted reproductive technology (ART), in vitro fertilisation (IVF) or intra cytoplasmic sperm injection (ICSI) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) FR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003787-24 | Sponsor Protocol Number: PM-CARE-PNRR-MAD-2022-12375905 | Start Date*: 2023-04-20 | ||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
Full Title: Precision Medicine in patients with unresectable CholAngiocarcinoma; RadioEmbolization and combined biological therapy (Single arm, multicenter phase II study investigating the efficacy and safety... | ||||||||||||||||||
Medical condition: Unresectable intrahepatic cholangiocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004250-17 | Sponsor Protocol Number: RG_18-205,BN3010 | Start Date*: 2019-10-11 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: An International Prospective Trial on High-Risk Medulloblastoma in Patients Older than 3 Years | |||||||||||||
Medical condition: Histologically proven high-risk medulloblastoma, with any of the currently defined histological subtypes. High-risk disease is defined as patients with sonic hedgehog (SHH) subgroup or non-SHH/non-... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) AT (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) NO (Trial now transitioned) NL (Trial now transitioned) BE (Trial now transitioned) SE (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004868-30 | Sponsor Protocol Number: PNET5MB | Start Date*: 2013-10-31 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: AN INTERNATIONAL PROSPECTIVE TRIAL ON MEDULLOBLASTOMA (MB) IN CHILDREN OLDER THAN 3 TO 5 YEARS WITH WNT BIOLOGICAL PROFILE (PNET 5 MB – LR and PNET 5 MB – WNT-HR), AVERAGE-RISK BIOLOGICAL PROFILE (... | |||||||||||||
Medical condition: Children with medulloblastoma. Medulloblastoma is a highly cellular malignant embryonal neoplasm. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) FR (Trial now transitioned) FI (Trial now transitioned) SE (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) AT (Ongoing) NO (Completed) CZ (Trial now transitioned) NL (Trial now transitioned) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000988-26 | Sponsor Protocol Number: CITA06 | Start Date*: 2007-04-02 |
Sponsor Name:Portsmouth Hospitals NHS Trust | ||
Full Title: Cyclooxygenase inhibitor therapy in patients with oesophageal adenocarcinoma: A pilot study | ||
Medical condition: Oesophageal adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005019-14 | Sponsor Protocol Number: 12076 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: The short term effects of an AKT inhibitor (AZD5363) on biomarkers of the AKT pathway and anti-tumour activity in a breast cancer paired biopsy study (STAKT Trial) | |||||||||||||
Medical condition: primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005688-32 | Sponsor Protocol Number: CD-FNB | Start Date*: 2009-07-02 | |||||||||||
Sponsor Name:Univeristy Hospital Na Bulovce | |||||||||||||
Full Title: Biological therapy in the prevention of Crohn`s disease recurrence after resection in ileocecal region. | |||||||||||||
Medical condition: Prevention of Crohn`s disease recurrence after surgery in ileocecal region by postoperative application of infliximab (four infusions). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002138-20 | Sponsor Protocol Number: CURTAXEL | Start Date*: 2013-10-09 | |||||||||||
Sponsor Name:Centre Jean Perrin | |||||||||||||
Full Title: Multicenter randomized phase II study, double-blind, comparing Taxotere plus curcumin versus Taxotere plus placebo combination in first-line treatment of prostate cancer metastatic castration resis... | |||||||||||||
Medical condition: metastatic prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001244-15 | Sponsor Protocol Number: D22-P006 | Start Date*: 2023-01-12 |
Sponsor Name:GHU Paris Psychiatrie et Neurosciences | ||
Full Title: Efficiency of a composite personalised care on functional outcome in early psychosis: A Prospective Randomised Controlled Trial - PsyCARE_Trial | ||
Medical condition: early psychosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001569-33 | Sponsor Protocol Number: LLC-R-FCM-1 | Start Date*: 2005-09-23 |
Sponsor Name:Dept. Hematology, Hospital Clinic | ||
Full Title: First line treatment with rituximab plus fludarabine, cyclophosphamide, mitoxantrone (R-FCM) and maintenance therapy with rituximab in patients diagnosed with chronic lymphocytic leukemia. Tratamie... | ||
Medical condition: Patients diagnosed with chronic lymphocytic leukemia (CLL) according to the WHO guidelines, within 18 and 71 years and not previously treated | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000317-22 | Sponsor Protocol Number: BRE-ASA01 | Start Date*: 2017-04-13 |
Sponsor Name:Linköping University | ||
Full Title: A pilot study of low dose acetylsalicylic acid (ASA) for reduction of breast density and inflammation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006646-12 | Sponsor Protocol Number: POMAlternative | Start Date*: 2024-04-25 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Alternative dosing scheme of pomalidomide 4 mg every other day versus pomalidomide 2 mg and 4 mg every day: reduction in costs, same efficacy? A PKPD bioequivalence pilot study. | ||
Medical condition: Multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005582-36 | Sponsor Protocol Number: SIM-07-003 | Start Date*: 2008-04-07 |
Sponsor Name:DEFIANTE FARMACEUTICA,LDA | ||
Full Title: A RANDOMIZED MULTICENTRE PHASE II STUDY TESTING TOLERABILITY AND EFFICACY ON SURROGATE ENDPOINTS (LIPID PROFILE, VASCULAR INFLAMMATORY MARKERS AND THROMBOGENESIS) OF SIMVAPUFA FORMULATION (ASSOCIAT... | ||
Medical condition: For this study, patients with acute coronary syndrome STEMI (ST-Elevation Myocardial Infarction and NSTEMI (Non-ST-Elevation Myocardial Infarction), occurred within the previous 72 hours with posit... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
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