- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Tubulointerstitial nephritis.
Displaying page 1 of 1.
EudraCT Number: 2017-000992-10 | Sponsor Protocol Number: FHM-1-2017 | Start Date*: 2017-06-28 | |||||||||||||||||||||
Sponsor Name:Universitets klinik for nyresygdomme og Hypertension | |||||||||||||||||||||||
Full Title: Prednisolone treatment in acute interstitial nephritis | |||||||||||||||||||||||
Medical condition: Acute interstitial nephritis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005956-18 | Sponsor Protocol Number: TIN | Start Date*: 2008-01-18 | |||||||||||
Sponsor Name:Timo Jahnukainen | |||||||||||||
Full Title: Tubulointerstitiaalinefriitti - Riskitekijöiden kartoitus ja lääkehoidon vaikutus sairauden kulkuun. | |||||||||||||
Medical condition: Tubulointerstitiaalinefriittiä sairastavat lapset | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003364-51 | Sponsor Protocol Number: AUR-VCS-2012-01 | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:Aurinia Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomized, Controlled Double-blind Study Comparing the Efficacy and Safety of Voclosporin (23.7 mg BID, or 39.5 mg BID) with Placebo in Achieving Remission in Patients with Active Lupus Nephritis | |||||||||||||
Medical condition: Active lupus nephritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004973-29 | Sponsor Protocol Number: CL3-78989-019 | Start Date*: 2014-08-13 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A safety open-label study of Gevokizumab in the treatment of patients with chronic non-infectious Uveitis disease, an eXtension study. The EYEGUARD-X study. | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: chronic non-infectious uveitis | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) PT (Completed) ES (Completed) AT (Completed) GR (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001610-42 | Sponsor Protocol Number: X052130/CL3-78989-005 | Start Date*: 2013-01-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:XOMA (US) LLC | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-masked, Placebo-controlled Study of the Safety and Efficacy of Gevokizumab in the Treatment of Active Non-infectious Intermediate, Posterior, or Pan- Uveitis | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Non-infectious Intermediate, Posterior, or Pan- Uveitis | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) PT (Completed) GB (Prematurely Ended) ES (Completed) GR (Prematurely Ended) AT (Completed) PL (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001609-25 | Sponsor Protocol Number: X052131/CL3-78989-006 | Start Date*: 2013-01-02 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:XOMA (US) LLC | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A RandomizEd, Double-masked, Placebo-controlled Study of the SafetY and Efficacy of GevokizUmAb in the TReatment of Subjects with Non-infectious IntermeDiate, Posterior, or Pan- uveitis Currently C... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Non-infectious Intermediate, Posterior, or Pan- Uveitis | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) PT (Completed) IT (Completed) GR (Prematurely Ended) ES (Completed) PL (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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