- Trials with a EudraCT protocol (1,556)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,556 result(s) found for: Alkaline phosphatase.
Displaying page 1 of 78.
| EudraCT Number: 2019-004826-12 | Sponsor Protocol Number: MAP4B-safety | Start Date*: 2021-07-27 |
| Sponsor Name:Association of Dutch Burn Centres | ||
| Full Title: Safety and preliminary efficacy of Alkaline Phosphatase in severely burned patients | ||
| Medical condition: Severe Burns | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002663-33 | Sponsor Protocol Number: NUH-ALS-2015-04 | Start Date*: 2018-11-05 | |||||||||||
| Sponsor Name:Alloksys Life Sciences BV | |||||||||||||
| Full Title: Preventing Oxidative stress induced Ischemic Injury and Systemic Inflammation complications during and after invasive Cardiac surgery with Alkaline Phosphatase (APPIRED III) | |||||||||||||
| Medical condition: systemic inflammation as side-effect of heart-lung machine during cardiac surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) NL (Completed) AT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004737-85 | Sponsor Protocol Number: 1.3 | Start Date*: 2018-12-11 |
| Sponsor Name:Amsterdam UMC, location VUmc | ||
| Full Title: Alkaline Phosphatase to prevent ischemia reperfusion injury in living kidney transplantation | ||
| Medical condition: Ischemia reperfusion injury in living donor kidney transplantation | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-024013-31 | Sponsor Protocol Number: CBPS804A2202 | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: An open-label, intra-patient dose-escalation study to evaluate the safety and tolerability, pharmacokinetics, pharmacodynamics and preliminary efficacy of multiple infusions of BPS804 in adults wit... | |||||||||||||
| Medical condition: Hypophosphatasia (HPP) is a rare genetic metabolic disorder which results in impaired skeletal mineralization, and which is caused by the absence of or by deficient enzymatic activity of the tissue... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002276-17 | Sponsor Protocol Number: ET-B-025-02 | Start Date*: 2006-08-24 | |||||||||||
| Sponsor Name:Pharma Mar SA, Sociedad Unipersonal | |||||||||||||
| Full Title: Phase II Study of Yondelis® in Men with Advanced Prostate Carcinoma Estudio fase II con Yondelis en hombres con cáncer de próstata avanzado | |||||||||||||
| Medical condition: Advanced Prostate Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006767-14 | Sponsor Protocol Number: NL79196.018.21 | Start Date*: 2022-08-24 |
| Sponsor Name:Amsterdam UMC | ||
| Full Title: Alkaline Phosphatase as treatment of Ischemia Reperfusion Injury to prevent delayed graft function | ||
| Medical condition: ischemia reperfusion injury in kidneys transplanted from donors after cardiac death | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002505-10 | Sponsor Protocol Number: NL77754.018.21 | Start Date*: 2021-11-30 | |||||||||||||||||||||
| Sponsor Name:Amsterdam University Medical Centre | |||||||||||||||||||||||
| Full Title: Rescue Alkaline Phosphatase In Defense against all cause Acute Kidney Injury (RAPID-AKI) | |||||||||||||||||||||||
| Medical condition: Acute kidney injury | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2006-000769-13 | Sponsor Protocol Number: AP SEP 02-02 | Start Date*: 2006-06-13 |
| Sponsor Name:AM-Pharma | ||
| Full Title: A double-blind, randomized, placebo-controlled study to investigate the clinical efficacy and safety of two doses of Alkaline Phosphatase administered for three days in patients with severe sepsi... | ||
| Medical condition: Severe sepsis and septic shock | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-007406-11 | Sponsor Protocol Number: ENB-002-08 | Start Date*: 2009-02-25 | |||||||||||
| Sponsor Name:Enobia Canada Limited Partnership | |||||||||||||
| Full Title: A Multicenter, Open-Label Study of the Safety, Tolerability and Pharmacology of ENB-0040 (Enobia’s human recombinant tissue non-specific alkaline phosphatase fusion protein) in up to 6 Severely Aff... | |||||||||||||
| Medical condition: Infantile Hypophosphatasia | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003153-42 | Sponsor Protocol Number: ENB-008-10 | Start Date*: 2017-08-03 | |||||||||||
| Sponsor Name:Alexion Pharma GmbH | |||||||||||||
| Full Title: Extension Study of Protocol ENB-006-09 Evaluating the Long-Term Safety and Efficacy of Asfotase Alfa (Human Recombinant Tissue-Nonspecific Alkaline Phosphatase Fusion Protein) in Children with Hyp... | |||||||||||||
| Medical condition: Hypophosphatasia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001128-52 | Sponsor Protocol Number: ENB-006-09 | Start Date*: 2015-05-28 | |||||||||||
| Sponsor Name:Alexion Pharma International Sàrl | |||||||||||||
| Full Title: A Randomized, Open-Label, Multicenter, Multinational, Dose-Ranging, Historical Control Study of the Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of ENB-0040 (Human Recombinant Tissue-No... | |||||||||||||
| Medical condition: Hypophosphatasia (HPP) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019850-42 | Sponsor Protocol Number: ENB-010-10 | Start Date*: 2011-03-04 | |||||||||||
| Sponsor Name:Alexion Pharma GmbH | |||||||||||||
| Full Title: An Open-Label, Multicenter, Multinational Study of the Safety, Efficacy and Pharmacokinetics of Asfotase alfa (human recombinant tissue nonspecific alkaline phosphatase fusion protein) in Infants a... | |||||||||||||
| Medical condition: Hypophosphatasia is a rare inborn error of bone metabolism caused by inactivating mutations in the gene encoding the Tissue-nonspecific alkaline phosphatase isoenzyme. With deficiency of Tissue-... | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) IT (Completed) ES (Completed) FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001957-16 | Sponsor Protocol Number: BREAST-SK-001 | Start Date*: 2019-10-31 | |||||||||||
| Sponsor Name:Národný onkologický ústav | |||||||||||||
| Full Title: Phase II study of Vinorelbine, cisplatin, disulfiram and copper in CTC_EMT positive refractory metastatic breast cancer. | |||||||||||||
| Medical condition: breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SK (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004570-34 | Sponsor Protocol Number: 01045-ATLEP | Start Date*: 2018-11-15 | ||||||||||||||||
| Sponsor Name:Medical Center - University of Freiburg | ||||||||||||||||||
| Full Title: Phase II, Open-label, Study in Patients with anaplastic (ATC) or poorly differentiated thyroid carcinomas (PDTC) to investigate the Clinical Efficacy and Safety of the Combination Therapy of Lenvat... | ||||||||||||||||||
| Medical condition: Anaplastic (ATC) or Poorly Differentiated Thyroid Carcinoma (PDTC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-000761-40 | Sponsor Protocol Number: AP-recAP-AKI-02-01 | Start Date*: 2014-10-22 |
| Sponsor Name:AM-Pharma B.V. | ||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Four-Arm, Parallel-Group, Proof of Concept, and Dose-Finding Adaptive Phase 2a/2b Study to Investigate the Safety, Tolerability and Efficacy and Effe... | ||
| Medical condition: Sepsis-Associated Acute Kidney Injury | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) FI (Completed) CZ (Completed) AT (Completed) NL (Completed) ES (Completed) IT (Prematurely Ended) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001831-38 | Sponsor Protocol Number: ENB-009-10 | Start Date*: 2017-05-09 | |||||||||||
| Sponsor Name:Alexion Pharma GmbH | |||||||||||||
| Full Title: A Randomized, Open-Label, Multicenter, Multinational, Dose-Ranging, Concurrent Control Study of the Safety, Efficacy, and Pharmacokinetics of ENB-0040 (Human Recombinant Tissue-Nonspecific Alkaline... | |||||||||||||
| Medical condition: Hypophosphatasia | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000809-39 | Sponsor Protocol Number: AA-HPP-405 | Start Date*: 2016-02-04 | |||||||||||
| Sponsor Name:Alexion Pharma International Sàrl | |||||||||||||
| Full Title: An Open-label, Multicenter, Expanded Access Program for Asfotase Alfa (human recombinant tissue-nonspecific alkaline phosphatase fusion protein) Treatment for Patients with Infantile- or Juvenile-o... | |||||||||||||
| Medical condition: Hypophosphatasia | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007346-63 | Sponsor Protocol Number: ALS-003-2008 | Start Date*: 2011-04-05 |
| Sponsor Name:Alloksys Life Sciences B.V. | ||
| Full Title: Reumap: An Open Label phase II study of Bovine Intestinal Alkaline Phosphatase (bIAP), An Inflammation modulating moiety, in RA patients | ||
| Medical condition: Rheumatoid Arthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Temporarily Halted) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-009369-32 | Sponsor Protocol Number: ENB-003-08 | Start Date*: 2009-03-30 | |||||||||||
| Sponsor Name:Alexion Pharma GmbH | |||||||||||||
| Full Title: Extension Study of ENB-0040 (Human Recombinant Tissue-Nonspecific Alkaline Phosphatase Fusion Protein) in Severely Affected Infants and Young Children with Hypophosphatasia (HPP) | |||||||||||||
| Medical condition: Infantile hypoposphatasia | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000321-41 | Sponsor Protocol Number: ALENDROHNP2011 | Start Date*: 2012-04-18 | |||||||||||
| Sponsor Name:FUNDACION HOSPITAL NACIONAL DE PARAPLEJICOS PARA LA INVESTIGACIÓN Y LA INTEGRACIÓN | |||||||||||||
| Full Title: PREVENTIVE TREATMENT OF BONE MASS LOSS WITH ALENDRONATE AND CALCIFEDIOL IN PATIENTS WITH ACUTE SPINAL CORD INJURY | |||||||||||||
| Medical condition: Preventing loss of bone density in patients with spinal cord injury of traumatic etiology complete during the first year of evolution of the lesion. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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