- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
17 result(s) found for: Fibromatosis.
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EudraCT Number: 2011-006037-42 | Sponsor Protocol Number: IB2011-03 | Start Date*: 2013-09-06 | |||||||||||
Sponsor Name:Institut Bergonié | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005215-41 | Sponsor Protocol Number: 5.5 | Start Date*: 2017-05-05 | |||||||||||
Sponsor Name:Olli Leppänen | |||||||||||||
Full Title: DupuytrEn Treatment EffeCtiveness Trial (DETECT): a protocol for prospective, randomized, controlled, outcome assessor-blinded, three armed parallel 1:1:1, multicenter trial comparing efficacy and ... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006143-31 | Sponsor Protocol Number: AUX-CC-854.01 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A Phase 3, Open Label Study of Safety and Efficacy of AA4500 in the Treatment of Subjects With Dupuytren's Contracture | |||||||||||||
Medical condition: Dupuytren's Contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007872-99 | Sponsor Protocol Number: AUX-CC-860 | Start Date*: 2010-02-01 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: Long term follow up of subjects treated with AA4500 in studies AUX-CC-854, AUX-CC-856, AUX-CC-857/AUX-CC-858 and AUX-CC-859 | |||||||||||||
Medical condition: Dupuytren's contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005833-34 | Sponsor Protocol Number: AL-DES-01 | Start Date*: 2021-09-06 | |||||||||||
Sponsor Name:Ayala Pharmaceuticals, Inc. | |||||||||||||
Full Title: RINGSIDE: A Phase 2/3, Randomized, Multicenter Study to Evaluate AL102 in Patients with Progressing Desmoid Tumors | |||||||||||||
Medical condition: Progressing desmoid tumors | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Trial now transitioned) FR (Ongoing) PL (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001991-39 | Sponsor Protocol Number: NIR-DT-301 | Start Date*: 2019-07-26 |
Sponsor Name:SpringWorks Subsidiary 2, PBC | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Nirogacestat Versus Placebo in Adult Patients with Progressing Desmoid Tumors/Aggressive Fibromatosis (DT/AF). | ||
Medical condition: Desmoid Tumors/Aggressive Fibromatosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) NL (Completed) DE (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004239-37 | Sponsor Protocol Number: AUX-CC-810 | Start Date*: 2015-02-26 | ||||||||||||||||
Sponsor Name:Auxilium UK Limited | ||||||||||||||||||
Full Title: Long-term safety, curvature deformity characterization, and immunogenicity over time in subjects previously treated with AA4500 for Peyronie’s disease in studies AUX-CC-802, AUX-CC-803, AUX CC 804,... | ||||||||||||||||||
Medical condition: Peyronie's Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005065-21 | Sponsor Protocol Number: AUX-CC-862 | Start Date*: 2012-03-26 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: Retreatment of recurrent contractures in joints effectively treated with AA4500 (collagenase clostridium histolyticum [XIAFLEX®/XIAPEX®]) in an Auxilium-sponsored Phase 3 Study in the United States... | |||||||||||||
Medical condition: Dupuytren's contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004251-76 | Sponsor Protocol Number: 87230 | Start Date*: 2017-05-22 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: A pragmatic multi-centre randomised controlled non-inferiority, cost effectiveness trial comparing injections of collagenase into the cord to surgical correction in the treatment of moderate Dupuyt... | ||||||||||||||||||
Medical condition: Dupuytren's contracture | ||||||||||||||||||
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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: 2015-001780-40 | Sponsor Protocol Number: 11069 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | |||||||||||||
Full Title: A multi-centre, double blind, randomised, placebo-controlled, parallel group, phase II trial to determine the efficacy of intra-nodular injection of anti-TNF to control disease progression in early... | |||||||||||||
Medical condition: Dupuytren's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000666-17 | Sponsor Protocol Number: RR37_21_01 | Start Date*: 2022-07-30 | |||||||||||
Sponsor Name:Fidia Farmaceutici Spa | |||||||||||||
Full Title: A Phase II double-blind, randomised, placebo-controlled study of efficacy and safety of Vibrio alginolyticus collagenase administered to patients with Dupuytren contracture | |||||||||||||
Medical condition: Dupuytren contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000624-40 | Sponsor Protocol Number: CSTI571BDE70 | Start Date*: 2010-05-27 |
Sponsor Name:University of Heidelberg | ||
Full Title: PHASE II STUDY TO EVALUATE GLIVEC (IMATINIB MESYLATE) TO INDUCE PROGRESSION ARREST IN AGGRESSIVE FIBROMATOSIS / DESMOID TUMORS NOT AMENABLE TO SURGICAL RESECTION WITH R0 INTENT OR ACCOMPANIED BY UN... | ||
Medical condition: AGGRESSIVE FIBROMATOSIS / DESMOID TUMORS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006493-23 | Sponsor Protocol Number: NIMAO/2021-1/YG-01 | Start Date*: 2022-04-04 | ||||||||||||||||||||||||||
Sponsor Name:Nimes University Hospital | ||||||||||||||||||||||||||||
Full Title: Evaluation of the patient postoperative experience of two modes of WALANT-type anesthesia (lidocaine alone or combined with ropivacaine) used in ambulatory upper-extremity surgery | ||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002770-82 | Sponsor Protocol Number: RR202200317 | Start Date*: 2024-09-09 | |||||||||||
Sponsor Name:Universitair Medisch Centrum Groningen | |||||||||||||
Full Title: The use of FAPI-PET/CT scan and FDG-PET?CT scan in acute phase Peyronie's disease for detection of active fibroblasts and inflammation in the penis - a pilot study | |||||||||||||
Medical condition: Peyronie's disease | |||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022921-13 | Sponsor Protocol Number: AUX-CC-802 | Start Date*: 2011-01-24 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A PHASE 3, OPEN-LABEL STUDY OF THE SAFETY AND EFFECTIVENESS OF AA4500 ADMINISTERED TWICE PER TREATMENT CYCLE FOR UP TO FOUR TREATMENT CYCLES (2 x 4) IN MEN WITH PEYRONIE’S DISEASE | |||||||||||||
Medical condition: Peyronie's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DE (Completed) DK (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004091-19 | Sponsor Protocol Number: AUX-CC-867 | Start Date*: 2012-12-28 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A Phase 3b open-label, historically-controlled study to assess the safety and efficacy of two concurrent injections of AA4500 in adult subjects with multiple Dupuytren’s contractures with palpable ... | |||||||||||||
Medical condition: Dupuytren's contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006205-95 | Sponsor Protocol Number: 2011-006205-95 | Start Date*: 2012-10-05 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: Toremifene in desmoid tumor: prospective clinical trial and identification of potential molecular targets | |||||||||||||
Medical condition: Primary or recurrent sporadic desmoid tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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