- Trials with a EudraCT protocol (500)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
500 result(s) found for: Post and Core.
Displaying page 1 of 25.
EudraCT Number: 2013-002539-13 | Sponsor Protocol Number: CARE-ROP | Start Date*: 2014-04-01 | |||||||||||
Sponsor Name:University Medical Center Freiburg | |||||||||||||
Full Title: Multicenter randomized double masked parallel design exploratory study to assess safety and efficacy of two different doses of intravitreal anti-VEGF treatment with ranibizumab (0.12 mg vs. 0.20 mg... | |||||||||||||
Medical condition: retinopathy of prematurity | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003230-17 | Sponsor Protocol Number: CAIN457M2301E1 | Start Date*: 2020-01-22 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A Multicenter, Double-blind, Randomized Withdrawal extension study of subcutaneous secukinumab to demonstrate long-term efficacy, safety and tolerability in subjects with moderate to severe hidrade... | |||||||||||||
Medical condition: hidradenitis suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Ongoing) GR (Ongoing) ES (Ongoing) FR (Ongoing) PT (Ongoing) CZ (Ongoing) SK (Ongoing) LT (Ongoing) AT (Ongoing) NL (Ongoing) DK (Prematurely Ended) IT (Ongoing) HR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000668-17 | Sponsor Protocol Number: CZOL446H2301 E1 | Start Date*: 2005-07-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 3 year, double-blind extension to CZOL446H2301 to evaluate the long term safety and efficacy of zoledronic acid in the treatment of osteoporosis in postmenopausal women taking calcium and vitamin D. | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) BE (Completed) SE (Completed) FI (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011622-34 | Sponsor Protocol Number: CAIN457A2206E1 | Start Date*: 2010-04-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open label non-randomized extension study to evaluate the safety and tolerability of AIN457 (anti interleukin-17 monoclonal antibody) in patients with psoriatic arthritis | |||||||||||||
Medical condition: Psoriatic arthritis (PsA), which belongs to seronegative spondyloarthropathies (SpA). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005777-27 | Sponsor Protocol Number: M20-350 | Start Date*: 2021-10-08 |
Sponsor Name:AbbVie | ||
Full Title: A Multicenter, Single-Arm Prospective Study to Evaluate Safety and Efficacy of GLE/PIB 8-Week Treatment in Adults and Adolescents with Acute Hepatitis C Virus (HCV) Infection | ||
Medical condition: Hepatitis C Virus | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) AT (Ongoing) FR (Ongoing) IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002657-36 | Sponsor Protocol Number: HMRI2012101/1 | Start Date*: 2015-11-13 | |||||||||||
Sponsor Name:University of Newcastle | |||||||||||||
Full Title: Tenecteplase versus Alteplase for Stroke Thrombolysis Evaluation (TASTE) Trial | |||||||||||||
Medical condition: Acute Ischaemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) SE (Ongoing) FI (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001615-36 | Sponsor Protocol Number: ABY-035-002 | Start Date*: 2017-11-14 | |||||||||||
Sponsor Name:Affibody AB | |||||||||||||
Full Title: A phase II, randomized, parallel group, placebo-controlled, double-blinded, dose-finding study to evaluate efficacy, safety, tolerability, and pharmacokinetics of ABY-035 in subjects with moderate-... | |||||||||||||
Medical condition: moderate-to-severe plaque psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002363-22 | Sponsor Protocol Number: IIV-482 | Start Date*: 2021-05-27 |
Sponsor Name:National Institute for Public Health and the Environment | ||
Full Title: Vaccination of older persons against Sars-Cov-2 and cellular immunogenicity for long term protection (participating in the Doetinchem Cohort Study) | ||
Medical condition: SARS-CoV-19, frailty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003499-37 | Sponsor Protocol Number: DSC/11/2357/44 | Start Date*: 2013-01-20 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Long-term study evaluating the effect of Givinostat in patients with JAK2V617F positive chronic myeloproliferative neoplasms. | |||||||||||||
Medical condition: Chronic myeloproliferative neoplasms (cMPN). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) DE (Completed) PL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004182-26 | Sponsor Protocol Number: ELIA | Start Date*: 2009-02-02 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Antidepressive efficacy, safety, tolerability and genetic response predictors of lithium augmentation in Escitalopram-treated patients with major depression | ||
Medical condition: 30-40% of depressed patients do not respond to the first course of drug treatment chosen. Over 50% of nonresponders to the first treatment also do not respond to a second, different treatment . Of ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005899-36 | Sponsor Protocol Number: CLOU064C12301 | Start Date*: 2022-02-21 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double-blind, double-dummy, parallel-group study, comparing the efficacy and safety of remibrutinib versus teriflunomide in participants with relapsing multiple sclerosis, followed by... | |||||||||||||
Medical condition: Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Ongoing) IT (Ongoing) ES (Ongoing) NL (Ongoing) BE (Ongoing) BG (Ongoing) LV (Ongoing) HR (Ongoing) LT (Ongoing) AT (Ongoing) DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000661-19 | Sponsor Protocol Number: CFEM345EGB07 | Start Date*: 2005-11-04 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: Neoadjuvant hormone therapy for postmenopausal women with ER and/or PgR positive primary breast cancer: A multi-center study to determine the optimum length of treatment with Femara (letrozole 2.5m... | ||
Medical condition: Postmenopausal women with ER and/or PgR positive primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-005929-89 | Sponsor Protocol Number: CLOU064C12302 | Start Date*: 2022-02-01 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A randomized, double-blind, double-dummy, parallel-group study, comparing the efficacy and safety of remibrutinib versus teriflunomide in participants with relapsing multiple sclerosis, followed by... | ||
Medical condition: Multiple Sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) IT (Ongoing) GR (Ongoing) ES (Ongoing) PT (Ongoing) SI (Ongoing) SK (Ongoing) BG (Ongoing) PL (Ongoing) HR (Ongoing) EE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015508-24 | Sponsor Protocol Number: CAIN457C2301E1 | Start Date*: 2010-02-15 | ||||||||||||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||||||||||||
Full Title: Extensión de 38 semanas del Estudio Fase III, multicéntrico, aleatorizado con doble enmascaramiento, controlado con placebo, de determinación de dosis y 24 semanas de duración, con el objetivo de e... | ||||||||||||||||||||||||||||
Medical condition: Terapia adyuvante para el tratamiento de uveitis intermedia, uveitis posterior o panuveitis que precisen inmunosupresión sistémica | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002467-26 | Sponsor Protocol Number: 480-SFA2013-001 | Start Date*: 2013-08-30 |
Sponsor Name:480 Biomedical, Inc. | ||
Full Title: The SPRINT trial: An Evaluation of the 480 Biomedical STANZA™ Drug-Eluting Resorbable Scaffold (DRS) System v1.2 in the Treatment of de novo SFA Lesions | ||
Medical condition: An evaluation of the safety and performance of the STANZA DRS v1.2 system for the treatment of patients with obstructive superficial femoral artery disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011591-30 | Sponsor Protocol Number: CAIN457A2209E1 | Start Date*: 2010-09-21 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label non-randomized extension study to evaluate the safety and tolerability of AIN457 (anti interleukin-17 monoclonal antibody) in patients with moderate to severe ankylosing spondylitis | |||||||||||||
Medical condition: Ankylosing spondylitis (AS), which belongs to seronegative spondyloarthropathies (SpA). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004727-18 | Sponsor Protocol Number: CORUNO/II/05.1 | Start Date*: 2008-06-20 | |||||||||||
Sponsor Name:THERABEL PHARMACEUTICAL Ltd | |||||||||||||
Full Title: EFFECT OF MOLSIDOMINE 16 MG ADMINISTERED ONCE-DAILY AS A LONG-TERM ADD-ON TREATMENT, ON ATHEROSCLEROSIS PROGRESSION AND INFLAMMATORY BIOMARKERS IN PATIENTS HOSPITALIZED FOR ACUTE CORONARY SYNDROME. | |||||||||||||
Medical condition: Randomized, double-blind, placebo-controlled, add-on study in two parallel groups. Patients admitted for Non ST Segment Elevation Acute Coronary Syndromes will undergo a coronary angiography accord... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021900-93 | Sponsor Protocol Number: CLIN1001 PCM301 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:STEBA BIOTECH SA | |||||||||||||
Full Title: A European randomised Phase 3 study to assess the efficacy and safety of TOOKAD® Soluble for low risk localised prostate cancer compared to Active Surveillance | |||||||||||||
Medical condition: Low-risk prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) DE (Completed) NL (Completed) BE (Completed) SE (Completed) FI (Completed) DK (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003620-16 | Sponsor Protocol Number: IIV-465 | Start Date*: 2021-05-27 |
Sponsor Name:National Institute of Health and the Environment | ||
Full Title: Vaccine immunogenicity in Dutch frail versus non-frail older individuals (participating in the Doetinchem Cohort study) | ||
Medical condition: Older adults 73-79 years of age, birth cohorts year 1941-1947, still participating in round 6 of the Doetinchem Cohort Study. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013901-33 | Sponsor Protocol Number: CAIN457C2303E1 | Start Date*: 2009-11-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 38-week extension to a 24 week multicenter, randomized, double-masked, placebo controlled study to assess the difference in the rate of recurrent exacerbations in Behçet’s patients with posterior... | |||||||||||||
Medical condition: Adjunctive therapy to standard-of-care for the treatment of posterior uveitis or panuveitis secondary to Behçet's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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