- Trials with a EudraCT protocol (372)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
372 result(s) found for: Research Registry.
Displaying page 1 of 19.
EudraCT Number: 2018-003662-14 | Sponsor Protocol Number: GN17CA082 | Start Date*: 2019-05-13 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Patiromer-facilitated, dose-escalation of mineralocorticoid antagonists for the management of worsening congestion in people with heart failure and hyperkalaemia. A Phase IV, registry-based, rand... | |||||||||||||
Medical condition: People with heart failure, worsening symptoms and signs of congestion and serum potassium >5mmol/L | |||||||||||||
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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: 2017-000487-15 | Sponsor Protocol Number: CLSYN.1702 | Start Date*: 2018-12-21 | |||||||||||
Sponsor Name:Hamilton Health Sciences Corporation through its Population Health Research Institute | |||||||||||||
Full Title: CLEAR SYNERGY (OASIS 9) A 2x2 factorial randomized controlled trial of CoLchicine and spironolactonE in patients with ST elevation myocARdial infarction/SYNERGY Stent Registry – Organization to Ass... | |||||||||||||
Medical condition: ST segment Elevation Myocardial Infarction (STEMI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FI (Completed) CZ (Completed) NL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005159-15 | Sponsor Protocol Number: DORI-NOS-1008 | Start Date*: 2012-03-05 |
Sponsor Name:Johnson & Johnson Pharmaceutical Research & Development, L.L.C. | ||
Full Title: An Open-Label, Parallel-Group Study to Evaluate the Single-Dose Pharmacokinetics and Safety of Doripenem in Pediatric Patients 3 Months to 17 Years of Age, Inclusive | ||
Medical condition: Bacterial infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2019-003084-21 | Sponsor Protocol Number: cHL-PG01 | Start Date*: 2020-01-13 | |||||||||||
Sponsor Name:PROF.BRUNANGELO FALINI, DR.ENRICO TIACCI. DIPARTIMENTO DI MEDICINA, UNIVERSITA' DI PERUGIA | |||||||||||||
Full Title: A phase-II academic trial testing, in two parallel non-randomized cohorts, the combination of ruxolitinib (JAK1/2 inhibitor) with brentuximab or nivolumab in relapsed or refractory classical Hodgki... | |||||||||||||
Medical condition: Patients with relapsed or refractory cHL that has not responded to, or has progressed after, the previous treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005210-18 | Sponsor Protocol Number: EFFIPEC01 | Start Date*: 2021-03-28 | |||||||||||
Sponsor Name:Uppsala University | |||||||||||||
Full Title: EFFIPEC – Efficacy of Hyperthermic Intraperitoneal Chemotherapy Single-arm Phase I study, followed by an open-label, randomized, controlled registry-based Phase III trial | |||||||||||||
Medical condition: Colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002019-16 | Sponsor Protocol Number: U-2015-030 | Start Date*: 2016-09-06 | |||||||||||
Sponsor Name:Uppsala Clinical Research center | |||||||||||||
Full Title: Spironolactone Initiation Registry Randomized Interventional Trial in Heart Failure with Preserved Ejection Fraction | |||||||||||||
Medical condition: Heart Failure with Preserved Ejection Fraction, HFPEF | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005243-28 | Sponsor Protocol Number: 212082PCR3010 | Start Date*: 2012-03-14 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3b Multicenter, Open-label Abiraterone Acetate Long-term Safety Study | |||||||||||||
Medical condition: Metastatic Castration-Resistant Prostate Cancer (PCR) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: BE (Completed) HU (Prematurely Ended) ES (Completed) AT (Completed) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000319-30 | Sponsor Protocol Number: SECTOR | Start Date*: 2022-03-09 |
Sponsor Name:Institut Klinické a Experimentální Medicíny | ||
Full Title: Assessment of association between 3rd dose of mRNA vaccine and risk of SARS-CoV-2 infection in kidney transplant recipients, safety and immunogenicity assessment. | ||
Medical condition: SARS-CoV-2 infection in kidney transplant recipients; safety, effectiveness and immunogenicity of 3rd dose of SARS-CoV-2 mRNA vaccine. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002185-40 | Sponsor Protocol Number: LSH-21-001 | Start Date*: 2022-10-06 |
Sponsor Name:Landspitali - The National University Hospital of Iceland | ||
Full Title: Comparison of the Effect of Allopurinol and Febuxostat on Urinary 2,8-Dihydroxyadenine Excretion and Plasma Levels in Patients with Adenine Phosphoribosyltransferase Deficiency: A Clinical Trial | ||
Medical condition: Adenine phosphoribosyltransferase deficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001222-42 | Sponsor Protocol Number: CAPSS-272 | Start Date*: 2015-04-24 |
Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | ||
Full Title: A double-blind trial comparing the efficacy, tolerability and safety of monotherapy topiramate versus phenytoin in subjects with seizures indicative of new onset epilepsy | ||
Medical condition: New onset epilepsy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-001223-23 | Sponsor Protocol Number: CAPSS-311 | Start Date*: 2015-04-24 |
Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | ||
Full Title: TOPAMAX (Topiramate) Initiated as Monotherapy in Epilepsy (TIME): A Multicenter, Outpatient, Open-Label, Study to Evaluate the Dosing, Effectiveness and Safety of TOPAMAX as Monotherapy in the Trea... | ||
Medical condition: New onset epilepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2010-023952-10 | Sponsor Protocol Number: GS-US-196-0140 | Start Date*: 2011-06-27 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating 16 and 24 Weeks of a Four-Drug Regimen and 24 Weeks of a Three-Drug Regimen of GS-9451, Peginterferon Alfa 2a (PEG, Pegasys... | |||||||||||||
Medical condition: Chronic Hepatitis C Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001735-22 | Sponsor Protocol Number: CNTO328SMM2001 | Start Date*: 2011-09-28 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Siltuximab (Anti IL 6 Monoclonal Antibody) in Subjects with High-risk Smoldering Multiple Myeloma | |||||||||||||
Medical condition: High-risk Smoldering Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) SE (Completed) FR (Completed) GR (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2024-000583-38 | Sponsor Protocol Number: 70033093THR1011 | Start Date*: 2024-12-20 | |||||||||||
Sponsor Name:Janssen Research & Development, LLC | |||||||||||||
Full Title: Open-label, Multi-center, Single-dose Phase 1 Study to Investigate the Pharmacokinetics, Safety, and Tolerability of Milvexian in Pediatric Patients From 28 Days to Less Than 18 Years of Age at Ris... | |||||||||||||
Medical condition: Thromboembolic Events | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001077-40 | Sponsor Protocol Number: T54/2015 | Start Date*: 2019-05-07 |
Sponsor Name:Turku University Hospital | ||
Full Title: INNOVATIVE STEROID TREATMENT TO REDUCE ASTHMA DEVELOPMENT IN CHILDREN AFTER FIRST-TIME RHINOVIRUS INDUCED WHEEZING – THE INSTAR STUDY | ||
Medical condition: First acute wheezing episode | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Trial now transitioned) NO (Trial now transitioned) SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002296-17 | Sponsor Protocol Number: GS-US-337-0121 | Start Date*: 2013-09-02 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Sofosbuvir/Ledipasvir Fixed-Dose Combination for 12 Weeks with Ribavirin or for ... | |||||||||||||
Medical condition: Chronic Genotype 1 Hepatitis C Virus Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004920-39 | Sponsor Protocol Number: 38518168ASH2001 | Start Date*: 2013-08-16 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel Group Study of JNJ-38518168 in Symptomatic Adult Subjects with Uncontrolled, Persistent Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003133-34 | Sponsor Protocol Number: OSU1 | Start Date*: 2012-02-29 |
Sponsor Name:A. Carlsson Research AB | ||
Full Title: The Effects of the Dopamine Stabilizer (-)-OSU6162 on Craving and Impulsivity in Alcohol Dependent Patients | ||
Medical condition: Alcohol dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001176-38 | Sponsor Protocol Number: CNTO1959HDS2001 | Start Date*: 2018-10-29 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Subjects with Moderate to Severe Hidradenitis Suppurativa | |||||||||||||
Medical condition: Moderate to Severe Hidradenitis Suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000975-33 | Sponsor Protocol Number: RDCRN_RKSC_6412 | Start Date*: 2013-11-19 |
Sponsor Name:Landspitali - The National University Hospital of Iceland | ||
Full Title: Novel Assays for the Determination of Urinary 2,8-Dihydroxyadenine and Other Key Urinary Purine Metabolites - Rare Diseases Clinical Research Network Protocol Version 1 | ||
Medical condition: Adenine phosphoribosyltransferase deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: View results |
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