- Trials with a EudraCT protocol (2,029)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,029 result(s) found for: Type III.
Displaying page 1 of 102.
EudraCT Number: 2010-021348-16 | Sponsor Protocol Number: HGT-SAN-067 | Start Date*: 2011-02-09 | ||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc | ||||||||||||||||||
Full Title: An Open-Label Extension of Study HGT-SAN-055 Evaluating Long Term Safety and Clinical Outcomes of Intrathecal Administration of rhHNS in Patients with Sanfilippo Syndrome Type A (MPS IIIA) | ||||||||||||||||||
Medical condition: Sanfilippo Syndrome Type A or Mucopolysaccharidosis (MPS IIIA) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003960-20 | Sponsor Protocol Number: SHP-610-201 | Start Date*: 2015-02-18 | ||||||||||||||||
Sponsor Name:Shire human Genetic Therapies, Inc. | ||||||||||||||||||
Full Title: A Open-Label Extension of Study HGT-SAN-093 Evaluating the Safety and Efficacy Study of HGT-1410 (Recombinant Human Heparan N Sulfatase) Administration via an Intrathecal Drug Delivery Device in... | ||||||||||||||||||
Medical condition: Sanfilippo Syndrome Type A or Mucopolysaccharidosis (MPS IIIA) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) NL (Completed) GB (Prematurely Ended) FR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001983-20 | Sponsor Protocol Number: NGLU-CL01-T | Start Date*: 2015-08-06 | ||||||||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc | ||||||||||||||||||
Full Title: A Phase I/II Open Label Study in Previously Studied, SBC-103 Treatment Naïve MPS IIIB Subjects to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics/Efficacy of SBC-103 Administered Int... | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis III, type B (MPS IIIB), Sanfilippo B | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000753-20 | Sponsor Protocol Number: NGLU-CL06 | Start Date*: 2016-08-16 | ||||||||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A PHASE I/II OPEN LABEL STUDY IN MPS IIIB SUBJECTS TO INVESTIGATE THE SAFETY, BIODISTRIBUTION, PHARMACOKINETICS, AND PHARMACODYNAMICS/EFFICACY OF SBC-103 ADMINISTERED INTRAVENOUSLY | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis III, type B (MPS IIIB), Sanfilippo B | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004153-17 | Sponsor Protocol Number: 20171012 | Start Date*: 2018-05-03 | ||||||||||||||||||||||||||
Sponsor Name:Copenhagen Neuromuscular Center | ||||||||||||||||||||||||||||
Full Title: Evaluation of the effect of Triheptanoin on fatty acid oxidation and exercise tolerance in patients with debrancher deficiency, glycogenin-1 deficiency and phosphofructokinase deficiency at rest an... | ||||||||||||||||||||||||||||
Medical condition: Cori Forbe's Disease Also called: glycogen storage disease Type III or debrancher deficiency. Tarui's disease Also called: glycogen storage disease Type VII or phosphofructokinase deficiency. ... | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003450-24 | Sponsor Protocol Number: HGT-SAN-093 | Start Date*: 2014-04-09 | ||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc | ||||||||||||||||||
Full Title: A Randomized, Controlled, Open-label, Multicenter, Phase IIb Safety and Efficacy Study of HGT-1410 (Recombinant Human Heparan N Sulfatase) Administration via an Intrathecal Drug Delivery Device in ... | ||||||||||||||||||
Medical condition: Sanfilippo Syndrome Type A or Mucopolysaccharidosis (MPS IIIA) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) NL (Completed) IT (Completed) FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000903-19 | Sponsor Protocol Number: UX053-CL101 | Start Date*: 2022-08-24 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
Full Title: A Phase 1/2 First-in-human, 2-part Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses (Part 1: Open-label) and Repeat Doses (Part 2: Randomized, Double-blind... | |||||||||||||
Medical condition: Glycogen Storage Disease Type III (GSD III) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) IT (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004661-34 | Sponsor Protocol Number: 2006.426/19 | Start Date*: 2006-12-08 | |||||||||||
Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
Full Title: Evaluation d’un traitement par miglustat (Zavesca®) chez les patients atteints de mucopolysaccharidose de type III (maladie de Sanfilippo). Essai thérapeutique de phase IIb randomisé en aveugle con... | |||||||||||||
Medical condition: Mucopolysaccharidose de type III | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002762-33 | Sponsor Protocol Number: AX250-401 | Start Date*: 2022-12-12 | ||||||||||||||||
Sponsor Name:Allievex Corporation | ||||||||||||||||||
Full Title: A Phase 3B/4 Open-Label Multicenter Study Extension Study to Further Evaluate Safety, Tolerability and Efficacy of Intracerebroventricular AX 250 Treatment in Mucopolysaccharidosis Type IIIB (MPS I... | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B, MPS IIIB) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Temporarily Halted) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000195-15 | Sponsor Protocol Number: P4-SAF-302 | Start Date*: 2018-12-27 | |||||||||||
Sponsor Name:Lysogene SA | |||||||||||||
Full Title: An Open-Label, Single-Arm, Multicenter Study of Intracerebral Administration of Adeno-Associated Viral Vectors Serotype rh10 Carrying the Human N-sulfoglucosamine sulfohydrolase (SGSH) cDNA for the... | |||||||||||||
Medical condition: Mucopolysaccharidosis Type IIIA | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) NL (Temporarily Halted) DE (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015984-15 | Sponsor Protocol Number: HGT-SAN-055 | Start Date*: 2010-03-25 | ||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. (Shire HGT) | ||||||||||||||||||
Full Title: A Phase I/II Safety, Tolerability, Ascending Dose and Dose Frequency Study of Recombinant Human Heparan-N-sulfatase (rhHNS) Intrathecal Administration via an Intrathecal Drug Delivery Device in Pat... | ||||||||||||||||||
Medical condition: Sanfilippo Syndrome Type A or Mucopolysaccharidosis (MPS IIIA) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001479-18 | Sponsor Protocol Number: GENiSIS2013 | Start Date*: 2014-06-09 | |||||||||||
Sponsor Name:Manchester University NHS Foundation Trust | |||||||||||||
Full Title: A Phase III, Double Blinded, Randomised, Placebo Controlled Clinical Trial of High Dose Oral Genistein Aglycone in Patients with Sanfilippo Syndrome (Mucopolysaccharidosis III) | |||||||||||||
Medical condition: Sanfilippo syndrome (Mucopolysaccharidosis III) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019962-10 | Sponsor Protocol Number: P1-SAF301 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:SANFILIPPO Therapeutics SAS | |||||||||||||
Full Title: AN OPEN-LABEL, SINGLE ARM, MONOCENTRIC, PHASE I/II CLINICAL STUDY OF INTRACEREBRAL ADMINISTRATION OF ADENO-ASSOCIATED VIRAL VECTORS SEROTYPE 10 CARRYING THE HUMAN SGSH AND SUMF1 cDNAS FOR THE TREAT... | |||||||||||||
Medical condition: Sanfilippo type A syndrome (also named Mucopolysaccharidosis Type A) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000856-33 | Sponsor Protocol Number: 2012-40 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Institut Pasteur | |||||||||||||
Full Title: A phase I/II, open-label, study of intracerebral administration of adeno-associated viral vector containing the human alpha-N-acetylglucosaminidase cDNA in children with Sanfilippo type B syndrome | |||||||||||||
Medical condition: Mucopolysaccharidosis III B | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003083-13 | Sponsor Protocol Number: 250-202 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Allievex Corporation | ||||||||||||||||||
Full Title: A Multicenter, Multinational, Extension Study to Evaluate the Long-Term Safety and Efficacy of Intracerebroventricular AX 250 in Patients with Mucopolysaccharidosis Type IIIB (MPS IIIB, Sanfilippo ... | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis Type IIIB (Sanfilippo Syndrome Type B, MPS IIIB) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Temporarily Halted) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003400-39 | Sponsor Protocol Number: NGLU-CL02 | Start Date*: 2014-07-15 | ||||||||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase I/II Open Label Study in MPS IIIB Subjects to Investigate the Safety, Pharmacokinetics, and Pharmacodynamics/Efficacy of SBC-103 Administered Intravenously | ||||||||||||||||||
Medical condition: Mucopolysaccharidosis III, type B (MPS IIIB), Sanfilippo B | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Temporarily Halted) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000240-94 | Sponsor Protocol Number: CLEAR0001 | Start Date*: 2012-05-09 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: The Safety and Efficacy of The Histone Deacetylase Inhibitor Panobinostat for Purging HIV-1 from The Latent Reservoir (CLEAR) Study | ||||||||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) Infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004435-31 | Sponsor Protocol Number: MVC116278 | Start Date*: 2012-05-15 | |||||||||||
Sponsor Name:ViiV Healthcare UK Limited | |||||||||||||
Full Title: An Expanded Access Protocol for Subjects Who Have Completed Clinical Studies Involving Maraviroc. | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022775-57 | Sponsor Protocol Number: JF002 | Start Date*: 2011-06-09 | ||||||||||||||||||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Effects of Vitamin D supplementation on Vitamin D levels and immune activation in HIV infected individuals on antiretroviral therapy-A pilot study. | ||||||||||||||||||||||||||||
Medical condition: HIV infected patients with vitamin D defficiency | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008556-16 | Sponsor Protocol Number: PRADA | Start Date*: 2009-07-13 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Pharmacokinetic and safety study of RAltegravir and atazanavir in a once DAily dose regimen in HIV-1 in-fected patients (PRADA) | |||||||||||||
Medical condition: HIV infected patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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