- Trials with a EudraCT protocol (916)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
916 result(s) found for: Hereditary diseases.
Displaying page 1 of 46.
EudraCT Number: 2011-004104-38 | Sponsor Protocol Number: ARPA-IGF1-2011 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:FIBHULP | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002432-40 | Sponsor Protocol Number: 042/15 | Start Date*: 2016-03-03 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE "LA NOSTRA FAMIGLIA" - SEZIONE SCIENTIFICA I.R.C.C.S. "E.MEDEA" | ||||||||||||||||||
Full Title: Safety and Efficacy of yIFN treatment in Friedreich ataxia | ||||||||||||||||||
Medical condition: FRDA is a progressive neurodegenerative disease inherited as recessive trait. It manifests itself usually in adolescence and affects various systems including the central and peripheral nervous sys... | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001054-42 | Sponsor Protocol Number: CSL830_3002 | Start Date*: 2015-03-04 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: An open-label, randomized study to evaluate the long-term clinical safety and efficacy of subcutaneous administration of human plasma-derived C1-esterase inhibitor in the prophylactic treatment of ... | |||||||||||||
Medical condition: Hereditary Angioedema Types I and II | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003603-18 | Sponsor Protocol Number: 331-201 | Start Date*: 2022-10-06 | ||||||||||||||||
Sponsor Name:BioMarin Pharmaceutical Inc. | ||||||||||||||||||
Full Title: A Phase 1/2, Open-Label, Dose-Escalation Study to Determine the Safety, Tolerability, and Efficacy of BMN 331, an Adeno-Associated Virus (AAV) Vector-Mediated Gene Transfer of Human SERPING1, in Su... | ||||||||||||||||||
Medical condition: Hereditary Angioedema (HAE) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000605-24 | Sponsor Protocol Number: CSL312_2001 | Start Date*: 2018-12-20 | |||||||||||
Sponsor Name:CSL Behring LLC | |||||||||||||
Full Title: A multicenter, randomized, placebo-controlled, parallel-arm study to investigate the efficacy, pharmacokinetics, and safety of CSL312 in subjects with hereditary angioedema | |||||||||||||
Medical condition: Hereditary angioedema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023388-16 | Sponsor Protocol Number: SNT-III-004 | Start Date*: 2011-06-07 | |||||||||||
Sponsor Name:Santhera Pharmaceuticals (Switzerland) Limited | |||||||||||||
Full Title: A Phase IIIb Double-Blind, Randomised, Placebo-Controlled Study of Patient Reported Outcomes in Friedreich’s Ataxia Patients after withdrawal from Treatment with Idebenone (PROTI Study) | |||||||||||||
Medical condition: Friedreich`s Ataxia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Ongoing) DE (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000916-10 | Sponsor Protocol Number: CSL830_3001 | Start Date*: 2013-12-10 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, cross-over study to evaluate the clinical efficacy and safety of subcutaneous administration of human plasma-derived C1-esterase inhibitor in the pro... | |||||||||||||
Medical condition: Hereditary Angioedema (HAE) type I and II | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) IT (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003918-12 | Sponsor Protocol Number: CSL312_3002 | Start Date*: 2021-06-08 | |||||||||||
Sponsor Name:CSL Behring LLC | |||||||||||||
Full Title: An Open-label Study to Evaluate the Long-term Safety and Efficacy of CSL312 (Garadacimab) in the Prophylactic Treatment of Hereditary Angioedema | |||||||||||||
Medical condition: Hereditary angioedema | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004230-37 | Sponsor Protocol Number: BCX7353-312 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: An open-label study to provide berotralstat access to subjects with type 1 and 2 hereditary angioedema who were previously enrolled in berotralstat studies | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019670-32 | Sponsor Protocol Number: B1 | Start Date*: 2013-01-31 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Pharmacokinetics and Safety of Human Pasteurised C1-Inhibitor Concentrate (Berinert/CE1145) in Subjects with Congenital C1-INH Deficiency and Frequent Hereditary Angioedema (HAE) Attacks. | |||||||||||||
Medical condition: Hereditary Angioedema (HAE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003139-38 | Sponsor Protocol Number: CE1145_3003 | Start Date*: 2015-02-12 | |||||||||||
Sponsor Name:ZLB Behring GmbH | |||||||||||||
Full Title: Open-label extension study of CE1145 (Human pasteurized C1 esterase inhibitor concentrate) in subjects with congenital C1-INH deficiency and acute HAE attacks | |||||||||||||
Medical condition: Congenital C1-INH deficiency | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003281-27 | Sponsor Protocol Number: BCX7353-204 | Start Date*: 2017-12-27 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: An Open-Label study to Evaluate the Long-Term Safety of Daily Oral BCX7353 in subjects with Type I and II Hereditary Angioedema | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) DK (Completed) AT (Completed) ES (Completed) SK (Completed) PL (Completed) BE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000987-92 | Sponsor Protocol Number: C11209 | Start Date*: 2011-09-26 | |||||||||||
Sponsor Name:Pharming Technologies B.V. | |||||||||||||
Full Title: Open-label, phase II, single arm study to evaluate the safety, immunogenicity, pharmacokinetics and efficacy of recombinant human C1 inhibitor for the treatment of acute attacks in pediatric patien... | |||||||||||||
Medical condition: Attacks associated with hereditary angioedema (HAE) in pediatric population 2-13 years of age. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) CZ (Completed) SK (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000570-25 | Sponsor Protocol Number: CSL312_3001 | Start Date*: 2021-02-09 | |||||||||||
Sponsor Name:CSL Behring LLC | |||||||||||||
Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel-arm study to investigate the efficacy and safety of subcutaneous administration of CSL312 (garadacimab) in the prophylactic tr... | |||||||||||||
Medical condition: Hereditary angioedema | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) NL (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000171-36 | Sponsor Protocol Number: C20-54 | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:INSERM | |||||||||||||
Full Title: PHASE I-II EFFICACY-TOXICITY OF ARTESUNATE IN FRIEDREICH ATAXIA | |||||||||||||
Medical condition: Friedreich Ataxia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002655-26 | Sponsor Protocol Number: BCX4161-301 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: OPuS-2 A multicentre, randomised, double blind, placebo controlled, parallel group study to evaluate the efficacy and safety of two dose levels of BCX4161 for 12 weeks as an oral prophylaxis treatm... | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) BE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002621-98 | Sponsor Protocol Number: SHP643-302 | Start Date*: 2022-08-19 | ||||||||||||||||
Sponsor Name:Takeda | ||||||||||||||||||
Full Title: A Phase 3 Multi-center, Open-label Study to Evaluate the Efficacy and Safety of Lanadelumab (SHP643) in Japanese Subjects with Hereditary Angioedema | ||||||||||||||||||
Medical condition: Hereditary Angioedema (HAE) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002744-27 | Sponsor Protocol Number: CR01849 | Start Date*: 2011-11-01 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: Pharmacodynamic Studies of a Histone Deacetylase Inhibitor in FRDA | |||||||||||||
Medical condition: Friedreich’s ataxia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002618-38 | Sponsor Protocol Number: 721 | Start Date*: 2020-06-25 | |||||||||||
Sponsor Name:ASSOCIAZIONE "LA NOSTRA FAMIGLIA" - SEZIONE SCIENTIFICA I.R.C.C.S. "E.MEDEA" | |||||||||||||
Full Title: Clinical trial - phase II - to test safety and efficay of Etravirine's treatment in Friedreich Ataxia's patients | |||||||||||||
Medical condition: Friedreich's ataxia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002319-82 | Sponsor Protocol Number: BCX4161-203 | Start Date*: 2013-09-30 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2a double-blind placebo-controlled 2-period crossover study to evaluate the safety and efficacy of BCX4161 as a prophylactic treatment to reduce the frequency of attacks in subjects with he... | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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