- Trials with a EudraCT protocol (76)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
76 result(s) found for: Giant cell.
Displaying page 1 of 4.
EudraCT Number: 2006-006964-48 | Sponsor Protocol Number: 20040215 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-Label, Multi-Center, Phase 2 Safety and Efficacy Study of Denosumab (AMG 162) in Subjects with Recurrent or Unresectable Giant Cell Tumor (GCT) of Bone | |||||||||||||
Medical condition: Giant Cell Tumor (GCT) of bone | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002778-38 | Sponsor Protocol Number: CL2-78989-012 | Start Date*: 2013-11-11 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (IRIS) | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled proof-of concept study of the efficacy and safety of gevokizumab in the treatment of patients with giant cell arteritis | |||||||||||||
Medical condition: Giant cell arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Completed) GB (Completed) CZ (Completed) FI (Completed) DK (Prematurely Ended) BE (Completed) AT (Completed) IE (Prematurely Ended) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001606-16 | Sponsor Protocol Number: 20062004 | Start Date*: 2009-01-16 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-label, Multi-center, Phase 2 Study of Denosumab in Subjects with Giant Cell Tumor of Bone | |||||||||||||
Medical condition: Giant cell tumor of bone (GCTB) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) AT (Completed) FR (Completed) ES (Completed) GB (Completed) PL (Completed) IT (Completed) SE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005090-22 | Sponsor Protocol Number: 001 | Start Date*: 2012-02-28 | |||||||||||
Sponsor Name:Southend Hospital | |||||||||||||
Full Title: A study of efficacy and safety of delayed release prednisone in newly diagnosed cases of Giant Cell Arteritis | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002622-24 | Sponsor Protocol Number: CAIN457R1DE01 | Start Date*: 2022-06-09 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, parallel-group, double-blind, placebo-controlled, multicenter trial to investigate the efficacy and safety of subcutaneously administered secukinumab in patients with new-onset of gia... | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000622-26 | Sponsor Protocol Number: CNTO1959GCA2001 | Start Date*: 2020-12-07 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Participants with New-Onset or Relapsing Giant Cell Arteritis | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) DE (Completed) PL (Completed) BE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003275-17 | Sponsor Protocol Number: AMB-051-01 | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:AmMax Bio., Inc. | |||||||||||||
Full Title: An Adaptive, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Intra-articular AMB-05X Injections in Subjects with Tenosynovial Giant Cell Tumor ... | |||||||||||||
Medical condition: Tenosynovial Giant Cell Tumor of the Knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Ongoing) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002716-41 | Sponsor Protocol Number: ML39425 | Start Date*: 2017-05-24 | |||||||||||
Sponsor Name:ROCHE SAS | |||||||||||||
Full Title: AN EXTENSION STUDY TO EVALUATE LONG TERM SAFETY OF SUBCUTANEOUS TOCILIZUMAB IN PATIENTS WITH GIANT CELL ARTERITIS WHO HAVE COMPLETED WA28119 CORE STUDY IN FRANCE, AND SUBSEQUENTLY HAVING FLARE OR P... | |||||||||||||
Medical condition: Giant cell arteritis (GCA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005244-42 | Sponsor Protocol Number: 20159990 | Start Date*: 2018-06-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||||||||||||
Full Title: An Open-label, Multi-center, Phase 2 Study of Denosumab in Subjects with Giant Cell Rich Tumors of Bone. | |||||||||||||||||||||||||||||||||
Medical condition: Aneurysmal bone cysts, giant cell granuloma, other giant cell rich lesions (primary bone, non-malignant) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) FR (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002826-22 | Sponsor Protocol Number: BONNOTTE-PHRCN-2017 | Start Date*: 2019-03-07 | |||||||||||
Sponsor Name:CHU Dijon Bourgogne | |||||||||||||
Full Title: MEthotrexate versus TOcilizumab for treatment of GIant cell Arteritis: a multicenter, randomized, controlled trial | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004870-22 | Sponsor Protocol Number: AMB-051-02 | Start Date*: 2021-02-24 | |||||||||||
Sponsor Name:AmMax Bio., Inc. | |||||||||||||
Full Title: A Phase 2, Adaptive, Open-Label, Multiple-Dose, Dose-Escalation Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Intravenous AMB-05X in Subjects with Tenosynovial Giant... | |||||||||||||
Medical condition: Tenosynovial Giant Cell Tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001716-29 | Sponsor Protocol Number: SNX-301-020 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:SynOx Therapeutics Ltd | |||||||||||||
Full Title: A Phase III, Multicentre, Randomised, Double-Blind Study to Assess the Safety and Efficacy of Emactuzumab vs. Placebo in Subjects with Tenosynovial Giant Cell Tumour. | |||||||||||||
Medical condition: Tenosynovial Giant Cell Tumour | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) ES (Completed) IT (Prematurely Ended) PL (Prematurely Ended) AT (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002610-12 | Sponsor Protocol Number: CAIN457ADE11C | Start Date*: 2018-12-06 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, parallel-group, double-blind, placebo-controlled, multicenter phase 2 trial to investigate the safety and efficacy of secukinumab (AIN457) in patients with giant cell arteritis (TitAIN) | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005841-50 | Sponsor Protocol Number: P08270471 | Start Date*: 2008-11-17 | |||||||||||
Sponsor Name:Leids Universitair Medisch Centrum | |||||||||||||
Full Title: Adjuvant zoledronic acid in ‘high risk’ Giant Cell Tumour of bone (GCT) - A randomized phase II study - | |||||||||||||
Medical condition: high risk Giant Cell Tumour of bone | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001758-32 | Sponsor Protocol Number: 20140114 | Start Date*: 2017-08-29 |
Sponsor Name:Amgen, Inc. | ||
Full Title: Long-term Safety Follow-up of Subjects With Giant Cell Tumour of Bone Treated With Denosumab in Study 20062004 | ||
Medical condition: Giant Cell Tumour of Bone | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) PL (Completed) FR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000344-25 | Sponsor Protocol Number: 17-249 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Essai, randomisé, contrôlé, ouvert, de deux schémas standardisés de décroissance, respectivement rapide (nord-américain) et lent (européen), de cortisone dans l’artérite à cellules géantes. | |||||||||||||
Medical condition: Patients atteints d’artérite à cellules géantes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002988-18 | Sponsor Protocol Number: EFC15068 | Start Date*: 2018-11-26 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of sarilumab in patients with giant cell arteritis | |||||||||||||
Medical condition: Giant Cell Arteritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) DK (Completed) HU (Completed) FR (Completed) SE (Prematurely Ended) EE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) PT (Completed) SI (Completed) BE (Prematurely Ended) HR (Completed) GB (GB - no longer in EU/EEA) NO (Completed) FI (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006022-25 | Sponsor Protocol Number: WA28119 | Start Date*: 2013-05-05 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF TOCILIZUMAB IN SUBJECTS WITH GIANT CELL ARTERITIS | |||||||||||||
Medical condition: Giant cell arteritis (GCA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SE (Completed) AT (Completed) DE (Completed) DK (Completed) GB (Completed) PT (Completed) NL (Completed) ES (Completed) BE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006398-41 | Sponsor Protocol Number: E7438-M081-501 | Start Date*: 2022-01-27 | |||||||||||
Sponsor Name:Eisai Co., Ltd. | |||||||||||||
Full Title: A Post-marketing Observational Study of Tazemetostat on Safety in Patients With Relapsed or Refractory Follicular Lymphoma With EZH2 Gene Mutation in Japan | |||||||||||||
Medical condition: Lymphoma, Follicular | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003202-14 | Sponsor Protocol Number: PCYC-1141-CA | Start Date*: 2017-04-12 | |||||||||||
Sponsor Name:Pharmacyclics LLC | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination with Rituximab versus Placebo in Combination wit... | |||||||||||||
Medical condition: Follicular lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) CZ (Trial now transitioned) HU (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) NL (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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