- Trials with a EudraCT protocol (113)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
113 result(s) found for: Glycoprotein.
Displaying page 1 of 6.
EudraCT Number: 2011-001659-36 | Sponsor Protocol Number: 2011-001659-36 | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:ITALIAN SARCOMA GROUP | |||||||||||||
Full Title: ABCB1/P-glycoprotein as biological marker for treatment of patient with high grade osteosarcoma | |||||||||||||
Medical condition: Non metastatic osteosarcoma of the extremities | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000352-19 | Sponsor Protocol Number: MOG001 | Start Date*: 2022-01-17 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase 3, Pivotal Study With an Open-Label Extension Period to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants ... | |||||||||||||
Medical condition: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOG-AD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) FR (Ongoing) ES (Ongoing) SE (Ongoing) BE (Ongoing) PT (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002767-95 | Sponsor Protocol Number: 12/0161 | Start Date*: 2013-06-17 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Long term antibody response to CMV gB vaccine in patients requiring liver or renal transplant. A Phase II open, single-site study, in participants who received CMV gB vaccine or placebo in previous... | |||||||||||||
Medical condition: Cytomegalovirus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001411-82 | Sponsor Protocol Number: HIPRA-HH-1 | Start Date*: 2021-08-11 | |||||||||||
Sponsor Name:LABORATORIOS HIPRA, S.A. | |||||||||||||
Full Title: A phase I/IIa study to evaluate safety and immunogenicity of recombinant protein RBD fusion dimer candidate vaccine against SARS-CoV-2 in adult healthy volunteers. | |||||||||||||
Medical condition: SARS-CoV-2 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005024-37 | Sponsor Protocol Number: 202100647 | Start Date*: 2022-01-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Evaluation of [18F]MC225 to measure P-glycoprotein function in neurodegenerative disease | ||
Medical condition: - Alzheimer's disease - Mild Cognitive Impairment - Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019688-12 | Sponsor Protocol Number: abchits2010 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:Friedrich-Schiller University Jena, Clinic for Internal Medicine I | |||||||||||||
Full Title: Prospective placebo controlled trial: Detection of coronary microembolization by Doppler ultrasound in patients with stable angina pectoris during percutaneous coronary interventions under an adjun... | |||||||||||||
Medical condition: Up to 60 patients with stable angina pectoris and planned PCI at the University Clinic of Jena are randomly assigned to the glycoprotein IIb/IIIa receptor antagonist abciximab or placebo. Randomisa... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002385-32 | Sponsor Protocol Number: APHP211057 | Start Date*: 2022-08-31 |
Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | ||
Full Title: Immediate versus delayed treatment with azathioprine or rituximab in anti-myelin oligodendrocytes glycoprotein (anti-MOG) antibodies associated acute demyelinating syndromes in children: a randomiz... | ||
Medical condition: myelin oligodendrocytes glycoprotein antibody associated diseases (MOGAD) | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000914-19 | Sponsor Protocol Number: EPO-ANE-4008 | Start Date*: 2006-10-23 |
Sponsor Name:Janssen-Cilag International N.V., Turnhoutseweg 30, 2340 Beerse, Belgium | ||
Full Title: A randomized, open-label, multicenter study evaluating thrombovascular events in subjects with cancer receiving chemotherapy and administered epoetin alfa once or three times a week for the treatme... | ||
Medical condition: Anemia in cancer patients receiving chemotherapy MedDRA Version 5.1 : list of preferred terma used in the process of defining thrombotic vascular events, see investigators brochure epoetin alpha. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) GB (Completed) SK (Completed) GR (Completed) FR (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-003192-34 | Sponsor Protocol Number: WN43194 | Start Date*: 2022-02-21 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY, SAFETY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF SATRALIZUMAB AS MONOTHERAPY OR IN ADDITION T... | |||||||||||||
Medical condition: Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000744-34 | Sponsor Protocol Number: 204939 | Start Date*: 2019-06-28 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase III, randomized, observer-blind, placebo controlled, multicenter clinical trial to assess Herpes Zoster recurrence and the reactogenicity, safety and immunogenicity of GSK Biologicals’ Herp... | ||
Medical condition: Healthy volunteers (Prevention of Herpes Zoster) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005226-26 | Sponsor Protocol Number: HIPRA-HH-2 | Start Date*: 2021-11-15 | |||||||||||
Sponsor Name:HIPRA SCIENTIFIC | |||||||||||||
Full Title: A Phase IIb, double-blind, randomized, active controlled, multi-centre, non-inferiority trial followed by a Phase III, single arm, open label trial, to assess immunogenicity and safety of a booster... | |||||||||||||
Medical condition: SARS-CoV-2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004863-69 | Sponsor Protocol Number: 108494, 108516, 108518, 108520 | Start Date*: 2006-12-22 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, single-blind, randomized, controlled, multicentre vaccination study to evaluate the safety and immune response of the GSK Biologicals Zoster vaccine, gE/AS01B, and to compare 3 doses of... | ||
Medical condition: Primary immunization of healthy elderly subjects (60 to 69 and more than or equal to 70 years) against zoster | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) SE (Completed) CZ (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003137-42 | Sponsor Protocol Number: EPIFLUX | Start Date*: 2020-04-10 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Klinische Pharmakologie | ||
Full Title: Exploring P-glycoprotein-mediated efflux transport at the blood-brain barrier as a biomarker of drug-resistance in focal epilepsy | ||
Medical condition: Investigation in healthy volunteers and epilepsy patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001909-24 | Sponsor Protocol Number: Spartacus/007 | Start Date*: 2012-10-24 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: A Multi Center, Prospective, Observational, Open-label, Pharmacokinetic Study of Tacrolimus in Heart and Lung Transplantation Patients during the First Days after Transplantation | |||||||||||||
Medical condition: Heart and lung transplantation, first days after transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001658-14 | Sponsor Protocol Number: V920-012 | Start Date*: 2015-09-03 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a Subsidiary of Merck & Co. Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Placebo-Controlled, Clinical Trial to Study the Safety and Immunogenicity of Three Consistency Lot Doses and a High Dose of rVSV-ZEBOV-GP (V920 Ebola Vaccine) in Healthy Ad... | |||||||||||||
Medical condition: Prevention of Ebola infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023861-23 | Sponsor Protocol Number: EPU P61 | Start Date*: 2011-01-31 |
Sponsor Name:Maastricht University | ||
Full Title: The effect of P-glycoprotein transport inhibition on brainmechanisms of sedation and cognitive impairment following antihistamines in healthy volunteers | ||
Medical condition: To assess the effects of inhibition of the P-glycoproteine transporter (by verapamil 120 mg) on cetirizine 15 mg in healthy volunteers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004401-26 | Sponsor Protocol Number: CT-830-04-0004 | Start Date*: 2005-03-21 |
Sponsor Name:STADA R&D GmbH | ||
Full Title: Evaluation of the Safety of a Formulation Containing Epoetin (Epoetin STADA) Administered Intravenously for the Maintenance Treatment of Renal Anemia: an Open Follow-up Trial. Study code (CRO) 411-... | ||
Medical condition: Anemia caused by terminal renal insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020759-30 | Sponsor Protocol Number: [11C]inhibitors | Start Date*: 2010-11-03 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: A pilot study to assess [11C]elacridar and [11C]tariquidar as two positron emission tomography radiotracers for visualization of P-glycoprotein in humans. | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002534-35 | Sponsor Protocol Number: 15022288 | Start Date*: 2005-09-14 |
Sponsor Name:Coombe Women's Hospital | ||
Full Title: Determination of plasma concentration of levobupivicaine following low concentration epidural infusion of levobupivicaine in pre-eclamptic and non pre-eclamptic nulliparous women. | ||
Medical condition: This clinical trial is an non-interventional observational clinical study, measuring the plasma levels of the levobupivicaine during labour with an epidural infusion. We will measure levels in pre-... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004610-26 | Sponsor Protocol Number: OVG2017/10 | Start Date*: 2018-11-28 | |||||||||||
Sponsor Name:Clinical Trials and Research Governance (CTRG), University of Oxford | |||||||||||||
Full Title: Evaluating the Long Term Immunogenicity of adenoviral and MVA vectored Ebola vaccine schedules and response to late boosting with AD26.ZEBOV vaccine: an open-label clinical trial | |||||||||||||
Medical condition: Ebola Virus Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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