- Trials with a EudraCT protocol (38)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38 result(s) found for: Certolizumab Pegol (CDP870).
Displaying page 1 of 2.
EudraCT Number: 2007-002716-26 | Sponsor Protocol Number: C87088 | Start Date*: 2008-01-22 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A phase IIIb, multinational, open-label, follow-on trial to C87085 designed to assess the long-term safety of certolizumab pegol, a pegylated Fab' fragment of a humanized anti TNF alpha monoclonal ... | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Prematurely Ended) HU (Completed) LV (Completed) EE (Completed) IT (Completed) CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002027-16 | Sponsor Protocol Number: RPCG06B2433 | Start Date*: 2006-12-12 |
Sponsor Name:UCB AE | ||
Full Title: Certolizumab pegol 400 mg monthly in the treatment of adult Greek patients with moderate to severe Crohn’s Disease, who have been previously treated successfully with infliximab but who have subseq... | ||
Medical condition: Certolizumab pegol in the treatment of adult Greek patients with moderate to severe Crohn’s Disease, who have been previously treated successfully with infliximab but who have subsequently lost the... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005025-20 | Sponsor Protocol Number: CR0012 | Start Date*: 2018-03-21 |
Sponsor Name:UCB Biosciences, Inc. | ||
Full Title: An open-label, multicenter study to assess the safety of certolizumab pegol in children and adolescents with active Crohn's Disease who completed C87035 or who were terminated from C87035 when the ... | ||
Medical condition: Crohn´s Disease | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-018027-33 | Sponsor Protocol Number: RA0043 | Start Date*: 2024-08-30 |
Sponsor Name:UCB BIOSCIENCES GmbH | ||
Full Title: A multicenter, open-label study to assess the pharmacokinetics, safety and efficacy of certolizumab pegol in children and adolescents with moderately to severely active polyarticular-course juvenil... | ||
Medical condition: Juvenile Idiopathic Arthritis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-003513-28 | Sponsor Protocol Number: PS0005 | Start Date*: 2015-03-27 | |||||||||||
Sponsor Name:UCB Biopharma, SPRL | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Parallel-group Study Followed by a Dose-blind Period and Open Label Follow-up to Evaluate the Efficacy and Safety of Certolizumab Pegol in Subjects... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005525-63 | Sponsor Protocol Number: C87044 | Start Date*: 2006-02-16 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Follow-up of study C87040 : Multicenter, single blind study to describe the efficacy and safety of re-treatment with CDP870 (certolizumab pegol) subcutaneous at 2 different dose regimens (400 mg i... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002141-39 | Sponsor Protocol Number: CDP870-040 | Start Date*: 2005-10-25 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: Multicenter, dose response, randomized, double blin, parallel, 3 arms, placebo controlled clinical trial to evaluate the efficacy and the safety of subcutaneous CDP870 (certolizumab pegol) at 2 dif... | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000830-38 | Sponsor Protocol Number: C87080 | Start Date*: 2008-10-07 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: A Phase IIIB, multi-centre open label, follow-up study to evaluate the safety and efficacy of certolizumab pegol administered concomitantly with DMARDs in subjects with active rheumatoid arthriti... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) AT (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003977-25 | Sponsor Protocol Number: C87043 | Start Date*: 2007-01-31 | |||||||||||
Sponsor Name:UCB S.A | |||||||||||||
Full Title: A phase III B multicentre open label 54 weeks clinical trial evaluating certolizumab pegol, a PEGylated Fab fragment of humanized antibody to tumor necrosis factor alpha (TNF alpha) on endoscopic a... | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002326-63 | Sponsor Protocol Number: CDP870-050 | Start Date*: 2005-09-21 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A Phase III Multi–center, Double–blind, Placebo–controlled, Parallel Group 24–Week Study to Assess the Efficacy and Safety of Two Dose Regimens of Liquid Certolizumab Pegol as Additional Medication... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SK (Completed) CZ (Completed) EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002629-30 | Sponsor Protocol Number: CDP870-051 | Start Date*: 2006-01-30 | |||||||||||
Sponsor Name:UCB Inc | |||||||||||||
Full Title: A Phase III Multi-center, Open-label, Follow-up Study, to Assess the Safety and Efficacy of Liquid Certolizumab Pegol as Additional Medication to Methotrexate, in the Treatment of Signs and Symptom... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SK (Completed) CZ (Completed) EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001913-41 | Sponsor Protocol Number: C87085 | Start Date*: 2007-12-12 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A phase IIIb, multinational, randomized, double-blind, placebo-controlled trial to assess the efficacy and safety of certolizumab pegol, a pegylated Fab' fragment of a humanized anti-TNF-alpha mono... | |||||||||||||
Medical condition: Crohn`s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) HU (Completed) LV (Completed) BE (Completed) EE (Completed) IT (Completed) DE (Completed) CZ (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001729-24 | Sponsor Protocol Number: C87046 | Start Date*: 2006-10-18 | |||||||||||
Sponsor Name:UCB S.A. | |||||||||||||
Full Title: Open label long term Clinical Trial Evaluating Efficacy and Safety of Chronic Therapy with certolizumab pegol, a PEGylated Fab fragment of humanized antibody to tumor necrosis factor alpha (TNF) in... | |||||||||||||
Medical condition: Patients with Crohn's disease and having completed C87042 study. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) AT (Completed) FR (Completed) SE (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004354-34 | Sponsor Protocol Number: C87047 | Start Date*: 2015-02-27 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A 26-week, multi-center, open-label study to investigate the efficacy and safety of CDP870 in active Crohn’s disease patients, who showed clinical efficacy in a remission induction study (Study C87... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001350-24 | Sponsor Protocol Number: CDP870-028 | Start Date*: 2005-05-31 | |||||||||||
Sponsor Name:UCB Celltech | |||||||||||||
Full Title: A Phase III multi-centre, open-label, follow-on study to CDP870-027, to assess the efficacy and safety of lyophilised CDP870 an engineered human anti-TNF PEG conjugate, dosed subcutaneously at 400 ... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) CZ (Completed) HU (Completed) LT (Completed) EE (Completed) LV (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004400-30 | Sponsor Protocol Number: C87048 | Start Date*: 2015-02-27 | |||||||||||
Sponsor Name:UCB Japan Co., Ltd. | |||||||||||||
Full Title: A multi-center, open-label study to investigate the efficacy and safety of CDP870 in active Crohn’s Disease patients, who showed no clinical efficacy in a remission induction study (Study C87037) b... | |||||||||||||
Medical condition: Crohn’s Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004104-37 | Sponsor Protocol Number: C87042 | Start Date*: 2006-03-23 | |||||||||||
Sponsor Name:UCB S.A. | |||||||||||||
Full Title: A Phase IIIb multicentre, open label induction and double blind comparison of two maintenance schedules evaluating clinical benefit and tolerability of certolizumab pegol, a pegylated Fab fragment ... | |||||||||||||
Medical condition: Patients with Crohn's Disease with prior loss of response or intolerance to infliximab | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) DE (Completed) AT (Completed) SE (Completed) DK (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003486-14 | Sponsor Protocol Number: PS0002 | Start Date*: 2015-04-27 | |||||||||||
Sponsor Name:UCB Biopharma, SPRL | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-group Study Followed by a Dose-blind Period and Open-label Follow-up to Evaluate the Efficacy and Safety of Certolizumab Pegol in Subjects... | |||||||||||||
Medical condition: Plaque Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003239-21 | Sponsor Protocol Number: C87091 | Start Date*: 2008-02-05 | |||||||||||
Sponsor Name:UCB PHARMA S.A. | |||||||||||||
Full Title: A phase IIIb, open label, randomized, exploratory clinical study exploring efficacy, safety and patients’ satisfaction with Certolizumab pegol treatment in moderate to severe Crohn’s disease when t... | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005288-86 | Sponsor Protocol Number: C87077 | Start Date*: 2009-03-18 | |||||||||||
Sponsor Name:UCB Pharma S.A. | |||||||||||||
Full Title: A Phase IIIb, open-label, run-in and double-blind, placebo-controlled, randomized study to evaluate the safety and efficacy of certolizumab pegol administered concomitantly with stable-dose methotr... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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