- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (38)
9 result(s) found for: tso.
Displaying page 1 of 1.
EudraCT Number: 2006-000720-13 | Sponsor Protocol Number: TSU-2/CDA | Start Date*: 2010-10-27 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomised, placebo-controlled, multi-centre phase II study to evaluate the efficacy and safety of three different dosages of oral Trichuris suis ova (TSO) suspension in active Crohn’... | |||||||||||||
Medical condition: Induction of remission in active Crohn´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015319-41 | Sponsor Protocol Number: TSO-MS | Start Date*: 2011-11-03 |
Sponsor Name:Charite Universitätsmedizin Berlin | ||
Full Title: Trichuris suis Oozyten (TSO®) in remittent-recurrent Multiple Sclerosis (MS) and Clinically Isolated Syndrom (CIS) | ||
Medical condition: remittent-recurrent Multiple Sclerosis (MS) and Clinically Isolated Syndrom (CIS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004772-65 | Sponsor Protocol Number: PROCTO | Start Date*: 2018-02-05 | |||||||||||
Sponsor Name:ParaTech A/S | |||||||||||||
Full Title: Probiotic Treatment of Ulcerative Colitis with Trichuris suis ova (TSO) | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006344-71 | Sponsor Protocol Number: TSORA | Start Date*: 2013-02-08 | |||||||||||
Sponsor Name:Immanuel Krankenhaus Berlin | |||||||||||||
Full Title: Trichuris suis ova (TSO) as a additional therapy for rheumatoid arthritis patients with insufficient response to methotrexate. A prospective, double-blind, randomized, controlled monocenter study. | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007549-29 | Sponsor Protocol Number: 2008-229 | Start Date*: 2009-06-09 | |||||||||||||||||||||
Sponsor Name:Danish Multiple Sclerosis Research Center | |||||||||||||||||||||||
Full Title: Trichuris suis Ova Therapy for Relapsing Multiple Sclerosis - a safety study | |||||||||||||||||||||||
Medical condition: Relapsing Multipel Sclerosis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006099-12 | Sponsor Protocol Number: TSO-01 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Statens Serum Institut | |||||||||||||
Full Title: Oral treatment of allergy with a non-pathogenic microorganism: A randomised clinical trial | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010282-23 | Sponsor Protocol Number: Bruxism-01 | Start Date*: 2010-10-26 | |||||||||||
Sponsor Name:Tandvården SU/Mölndal | |||||||||||||
Full Title: A randomized, open-label, cross-over study to explore a potential involvement of a dopamine related dysfunction as a mechanism behind bruxism | |||||||||||||
Medical condition: Patients with severe oral bruxism according to Polysomnographic cut-off criteria for bruxism: more than 4 bruxism episodes per hour, more than 6 bruxism bursts per episode and/or 25 bruxism bursts ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002711-25 | Sponsor Protocol Number: 039SC04253 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: DOSE-FINDING STUDY OF TRAZODONE IN THE TREATMENT OF PATIENTS WITH PRIMARY INSOMNIA | |||||||||||||
Medical condition: TREATMENT OF THE INSOMNIA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004738-39 | Sponsor Protocol Number: ENGOT-OV56/NSGO-CTU-DOVACC | Start Date*: 2021-08-20 | |||||||||||
Sponsor Name:Nordic Society of Gynaecological Oncology - Clinical Trial Unit | |||||||||||||
Full Title: ENGOT-OV56-NSGO-CTU-DOVACC. A Randomized Clinical Trial Investigating Olaparib, Durvalumab (MEDI4736) and UV1 as Maintenance Therapy in BRCAwt Patients with Recurrent Ovarian Cancer. | |||||||||||||
Medical condition: Ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) NO (Trial now transitioned) LT (Trial now transitioned) SE (Trial now transitioned) DE (Trial now transitioned) FI (Trial now transitioned) BE (Trial now transitioned) GR (Prematurely Ended) AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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