- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Mannose.
Displaying page 1 of 1.
EudraCT Number: 2021-003466-12 | Sponsor Protocol Number: MCMK0220 | Start Date*: 2022-03-25 | |||||||||||
Sponsor Name:MCM Klosterfrau Vertriebsgesellschaft mbH | |||||||||||||
Full Title: A double-blind, randomised, multi-centre, controlled clinical trial to compare D-mannose versus antibiotic in the treatment of acute uncomplicated lower urinary tract infections in female patients | |||||||||||||
Medical condition: acute uncomplicated lower urinary tract infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022085-26 | Sponsor Protocol Number: rhLAMAN-03 | Start Date*: 2010-10-05 |
Sponsor Name:Zymenex A/S | ||
Full Title: A single center, randomized, open-label, multiple-dose study of the efficacy and long-term safety of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) for the treatment of patients with alph... | ||
Medical condition: Treatment of alpha-Mannosidosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005575-40 | Sponsor Protocol Number: UZB-VHH2-4 | Start Date*: 2023-02-15 |
Sponsor Name:UZ Brussel | ||
Full Title: A phase II study to evaluate the imaging potential of 68GaNOTA-Anti-MMR VHH2 for in vivo imaging of MMR-expressing Macrophages by means of Positron Emission Tomography (PET) in patients with non-s... | ||
Medical condition: Patients diagnosed with non-small cell lung cancer (NSCLC), planned for standard-of-care (SOC) surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001988-36 | Sponsor Protocol Number: CCD-LMZYMAA1-08 | Start Date*: 2016-10-05 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A 24-month Multicenter, Open-label Phase II Trial Investigating the Safety and Efficacy of Repeated velmanase alfa (recombinant human alpha-mannosidase) Treatment in Pediatric Patients below 6 year... | |||||||||||||
Medical condition: Alfa-mannosidosis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) AT (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005011-25 | Sponsor Protocol Number: PR88302 | Start Date*: 2008-02-13 | |||||||||||
Sponsor Name:Progen Pharmaceuticals Limited | |||||||||||||
Full Title: A prospective, randomised, double-blind, placebo-controlled, parallel-group, international multicentre phase III trial of PI-88 in the adjuvant treatment of post-resection hepatocellular carcinoma ... | |||||||||||||
Medical condition: post-resection hepatocellular carcinoma Carcinoma hepatocelular post-resección | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000321-31 | Sponsor Protocol Number: rhLAMAN-09 | Start Date*: 2013-06-07 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A multi-center, un-controlled, open-labeled trial of the long-term safety of Velmanase Alfa aftercare treatment of subjects with alpha-Mannosidosis whom previously participated in Velmanase Alfa - ... | |||||||||||||
Medical condition: Treatement of Alpha-Mannosidosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000942-77 | Sponsor Protocol Number: EFC14028 | Start Date*: 2016-07-15 | |||||||||||
Sponsor Name:Genzyme Corporation | |||||||||||||
Full Title: A Phase 3 Randomized, Multicenter, Multinational, Double-blinded Study Comparing the Efficacy and Safety of Repeated Biweekly Infusions of Avalglucosidase Alfa (neoGAA, GZ402666) and Alglucosidase ... | |||||||||||||
Medical condition: Pompe disease (acid alpha-glucosidase deficiency) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Prematurely Ended) SE (Prematurely Ended) NL (Completed) ES (Completed) CZ (Completed) DE (Completed) BE (Completed) AT (Completed) PL (Completed) IT (Completed) PT (Completed) BG (Completed) HU (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004355-40 | Sponsor Protocol Number: rhLAMAN-04 | Start Date*: 2012-01-17 |
Sponsor Name:Zymenex A/S | ||
Full Title: A multi-center, open-label trial of the long-term efficacy and safety of Lamazym for the treatment of patients with alpha-Mannosidosis. | ||
Medical condition: Treatement of Alpha-Mannosidosis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003950-15 | Sponsor Protocol Number: rhLAMAN-10 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Zymenex A/S | |||||||||||||
Full Title: A single center, open label clinical trial investigating the long-term efficacy of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) treatment in subjects with alpha-Mannosidosis who previo... | |||||||||||||
Medical condition: alpha-Mannosidosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001766-15 | Sponsor Protocol Number: MBL2012 | Start Date*: 2013-02-12 | ||||||||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestion de la Investigación en Salud de Sevilla | ||||||||||||||||||
Full Title: Impact of azithromycin as an immunomodulator in patients with recurrent pneumonia and deficit of mannose-binding LECITHIN (MBL2012) | ||||||||||||||||||
Medical condition: Pediatric patients with recurrent pneumonia and MBL deficiency. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000336-97 | Sponsor Protocol Number: rhLAMAN-07 | Start Date*: 2015-01-30 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A multi-center, un-controlled, open-labeled trial of the long-term safety of Lamazym aftercare treatment of subjects with alpha-Mannosidosis | |||||||||||||
Medical condition: Alpha-Mannosidosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001923-11 | Sponsor Protocol Number: Nef-202 | Start Date*: 2012-10-17 | |||||||||||
Sponsor Name:Pharmalink AB | |||||||||||||
Full Title: A Multicentre, Interventional Treatment, Randomised, Double-Blind, Single Group Assignment, Placebo Controlled Study to Evaluate the Efficacy and Safety of Two Different Doses of Nefecon® in Primar... | |||||||||||||
Medical condition: Primary IgA nephropathy patients at risk of developing end stage renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) CZ (Completed) DE (Completed) BE (Completed) SE (Completed) DK (Completed) IT (Completed) GB (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003475-21 | Sponsor Protocol Number: ACT14132 | Start Date*: 2017-05-17 | ||||||||||||||||
Sponsor Name:Genzyme Corporation | ||||||||||||||||||
Full Title: An Open-label Ascending Dose Cohort Study to Assess the Safety, Pharmacokinetics, and Preliminary Efficacy of Avalglucosidase Alfa (NeoGAA, GZ402666) in Patients with Infantile-onset Pompe Disease ... | ||||||||||||||||||
Medical condition: Pompe disease (acid alpha-glucosidase deficiency) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Ongoing) Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
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