- Trials with a EudraCT protocol (895)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (408)
895 result(s) found for: MD.
Displaying page 1 of 45.
EudraCT Number: 2011-001888-51 | Sponsor Protocol Number: 27109640 | Start Date*: 2011-09-12 |
Sponsor Name:Inpharm | ||
Full Title: | ||
Medical condition: low back pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000813-39 | Sponsor Protocol Number: H7T-MC-TABL | Start Date*: 2006-11-27 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Prasugrel in comparison to Clopidogrel for Inhibition of Platelet Activation and Aggregation (PRINCIPLE) - TIMI 44 | |||||||||||||
Medical condition: subjects undergoing elective cardiac catheterization with planned percutaneous coronary intervention (PCI) with coronary stenting. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002618-37 | Sponsor Protocol Number: H7T-MC-TABN | Start Date*: 2006-12-28 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Cross-Over Study Comparing the Pharmacodynamic Response in Subjects with Acute Coronary Syndrome Receiving 14 Days 10-mg Maintenance Dose Prasugrel (LY640315) versus 14 ... | |||||||||||||
Medical condition: subjects with acute coronary syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020939-40 | Sponsor Protocol Number: MD-Neo-Pilot | Start Date*: 2010-07-28 |
Sponsor Name:Medizinische Universität Wien,Univ.Klinik f.Kinder-u.Jugendheilkunde | ||
Full Title: Pilot Trial: Feasibility of Microdialysis for Pharmacokinetic Studies in Neonatal Patients | ||
Medical condition: The present pilot study intends to establish the logistics of MD measurements of antibiotics in subcutaneous tissue of neonatal intensive care patients. Antibiotic serum levels will be measured in ... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004064-29 | Sponsor Protocol Number: CS747S-B-U4003 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A PHARMACODYNAMIC EVALUATION OF SWITCHING FROM TICAGRELOR TO PRASUGREL IN SUBJECTS WITH STABLE CORONARY ARTERY DISEASE: 2ND SWITCHING ANTIPLATELET AGENTS (SWAP 2) | |||||||||||||
Medical condition: Stable Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000064-10 | Sponsor Protocol Number: Fistula-SD-MD | Start Date*: 2011-03-17 |
Sponsor Name:Med. Univ. Wien, Klinik für klinische Pharmakologie | ||
Full Title: Target site pharmacokinetics of linezolid or tigecycline in patients with severe skin and skin structure infections (SSSI) associated with chronic fistulas. | ||
Medical condition: The findings of the present study will enable assessing whether currently employed therapy regimens with linezolid or tigecycline provide effective antimicrobial concentrations at the target site o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-000062-35 | Sponsor Protocol Number: ThereIsNoSponsorInvolved | Start Date*: 2011-04-05 | |||||||||||
Sponsor Name:Mikko Pitkänen, MD, PhD | |||||||||||||
Full Title: Artikaiini 40mg ja kloroprokaiini 40 mg päiväkirurgisina spinaalipuudutteina (Lyhenne: A40C40) | |||||||||||||
Medical condition: Knee arthroscopy performed as day case surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002351-42 | Sponsor Protocol Number: VIB4920.P0.S1 | Start Date*: 2020-01-13 | |||||||||||
Sponsor Name:Viela Bio, Inc. | |||||||||||||
Full Title: An Observational, Follow-on Study to the MEDI4920 (D5100C00002) Study to Evaluate the Duration of Clinical and Pharmacodynamic Efficacy of 12 weeks of Treatment with VIB4920 in Subjects with Modera... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003318-26 | Sponsor Protocol Number: AS/NEPA/001 | Start Date*: 2015-12-11 | |||||||||||
Sponsor Name:ASSOCIAZIONE SALENTINA ANGELA SERRA ONLUS | |||||||||||||
Full Title: Phase II, open-label, not comparative, multicenter study of multiple doses of NEPA (Netupitant+Palonosetron) in preventing chemotherapy induced nausea and vomiting (CINV) in patient with Non Hodgki... | |||||||||||||
Medical condition: NON HODGKIN'S LYMPHOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001807-19 | Sponsor Protocol Number: TV50717-CNS-30081 | Start Date*: 2019-11-12 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: An Open-Label, Long-Term Safety, Tolerability, and Efficacy Study of TEV-50717 (Deutetrabenazine) for the Treatment of Dyskinesia in Cerebral Palsy in Children and Adolescents (Open RECLAIM-DCP) | |||||||||||||
Medical condition: Dyskinesia in cerebral palsy (DCP) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Prematurely Ended) DK (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005292-15 | Sponsor Protocol Number: H7T-MC-TABR & TABR (1) | Start Date*: 2006-03-02 | |||||||||||
Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||
Full Title: A Pharmacokinetic and Pharmacodynamic Comparison of Prasugrel (LY640315) versus Clopidogrel in Subjects with Stable Atherosclerosis | |||||||||||||
Medical condition: Stable atherosclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005142-12 | Sponsor Protocol Number: TMC207-C203 | Start Date*: 2005-06-25 |
Sponsor Name:Tibotec Pharmaceuticals Limited | ||
Full Title: An open-label study to evaluate the extended early bactericidal activity, safety, tolerability and pharmacokinetics of multiple doses (m.d.) of TMC207 oral solution (os) and isoniazid (JH), m.d. of... | ||
Medical condition: Tuberculosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005114-11 | Sponsor Protocol Number: FO1 | Start Date*: 2011-12-14 | |||||||||||
Sponsor Name:AZIENDA USL DI FORLI' | |||||||||||||
Full Title: Switching from clopidogrel to prasugrel to protect early invasive treatment in acute coronary syndromes | |||||||||||||
Medical condition: Patients with acute coronary syndromes without persistent ST-segment elevation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001324-36 | Sponsor Protocol Number: 1042-900 | Start Date*: 2015-06-05 | |||||||||||
Sponsor Name:Marinus Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Open-Label Proof-of-Concept Trial of Ganaxolone in Children with PCDH19 Female Pediatric Epilepsy | |||||||||||||
Medical condition: PCDH19 Female Pediatric Epilepsy (FPE) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003742-17 | Sponsor Protocol Number: TV50717-CNS-30080 | Start Date*: 2019-07-12 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of TEV-50717 (Deutetrabenazine) for the Treatment of Dyskinesia in Cerebral Palsy in Children and Adolescents | |||||||||||||
Medical condition: Dyskinesia in cerebral palsy (DCP) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003491-41 | Sponsor Protocol Number: AG-CLI-0206-LTFU | Start Date*: 2016-12-12 | |||||||||||
Sponsor Name:AnGes Inc. | |||||||||||||
Full Title: A Long Term Follow-up Study of AMG0001 in Subjects with Critical Limb Ischemia | |||||||||||||
Medical condition: Critical limb ischemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004433-93 | Sponsor Protocol Number: RIOTCSTUDY22017 | Start Date*: 2018-05-01 | ||||||||||||||||
Sponsor Name:Nicholas Stephen Macklon, Professor, MD, PhD | ||||||||||||||||||
Full Title: RIOT C: REDUCING THE IMPACT OF OVARIAN STIMULATION. NOVEL APPROACHES TO LUTEAL SUPPORT IN IVF. STUDY 2. | ||||||||||||||||||
Medical condition: Ovarian stimulation in oocyte donation | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004849-26 | Sponsor Protocol Number: Parachute04 | Start Date*: 2015-02-05 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: PARACHUTE-trial Prospective Analysis of an individualized dosing Regimen of ATG (Thymoglobulin) in Children Undergoing HCT: redUcing Toxicity and improving Efficacy – a single arm phase II study | ||||||||||||||||||
Medical condition: Leukemia and immunedeficiency syndromes | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003628-11 | Sponsor Protocol Number: TapOxy001 | Start Date*: 2011-10-26 |
Sponsor Name:University Hospital Schleswig Holstein Kiel, Clinic of Neurology | ||
Full Title: Tapentadol PR vs Oxycodon CR A pilotstudiy for a mechanism-orientated Therapy of peripheral chronic neuropathic pain syndrom | ||
Medical condition: Chronical neuropathic pain syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-001080-24 | Sponsor Protocol Number: NL76906.068.21 | Start Date*: 2021-04-08 |
Sponsor Name:Maastricht University | ||
Full Title: The effect of plant stanol ester consumption on the vaccination response to a COVID-19 vaccine | ||
Medical condition: COVID-19 vaccination respons of people with BMI 27-35 kg/m2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
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