- Trials with a EudraCT protocol (120)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
120 result(s) found for: Parathyroid hormone.
Displaying page 1 of 6.
EudraCT Number: 2015-000411-40 | Sponsor Protocol Number: Version1.0 | Start Date*: 2015-10-23 |
Sponsor Name:Department of Nuclear Medicine and Endocrinology, Paracelsus Medical University Salzburg | ||
Full Title: Comparison of the detection of parathyroid adenoms using Tc-99m MIBI scintigraphy and F-18 Choline PET/CT in patients with primary hyperparathyroidism | ||
Medical condition: Primary hyperparathyroidism due to parathyroid adenoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003067-36 | Sponsor Protocol Number: SHP634-404 | Start Date*: 2018-06-28 | |||||||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||||||||||||
Full Title: An Open-label Study Investigating the Safety and Efficacy of rhPTH(1-84) in Subjects with Hypoparathyroidism. | |||||||||||||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001265-40 | Sponsor Protocol Number: PAR-C10-009 | Start Date*: 2011-07-29 | |||||||||||
Sponsor Name:NPS Pharmaceuticals, Inc. | |||||||||||||
Full Title: A 6-Month Open-label Study Investigating the Safety and Tolerability of NPSP558, a Recombinant Human Parathyroid Hormone (rhPTH [1-84]), for the Treatment of Adults with Hypoparathyroidism - A Clin... | |||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000284-32 | Sponsor Protocol Number: SHP634-401 | Start Date*: 2018-02-05 | |||||||||||||||||||||
Sponsor Name:Shire Human Genetic Therapies, Inc. | |||||||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Adaptive Study to Evaluate Symptom Improvement and Metabolic Control Among Adult Subjects With Symptomatic Hypoparathyroidism Treated With Recombinan... | |||||||||||||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) SE (Completed) DK (Completed) ES (Completed) NO (Completed) PT (Completed) BE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003108-22 | Sponsor Protocol Number: PAR-C14-007 | Start Date*: 2015-12-08 |
Sponsor Name:NPS Pharmaceuticals, Inc. | ||
Full Title: An Open-label, Single-dose Study to Determine the Pharmacokinetic/Pharmacodynamic Profile of Parathyroid Hormone (rDNA) Administered Subcutaneously at a Dose of 50 µg in Subjects with Hypoparathyr... | ||
Medical condition: Chronic hypoparathyroidism | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002729-31 | Sponsor Protocol Number: PETCOLINA1-FINBA | Start Date*: 2020-03-02 | |||||||||||
Sponsor Name:Fundación para la Investigación y la Innovación Biosanitaria del Principado de Asturias (FINBA) | |||||||||||||
Full Title: 18F-fluorocholine PET/CT in primary hyperparathyroidism with negative preoperative localization | |||||||||||||
Medical condition: Primary hyperthyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005063-34 | Sponsor Protocol Number: CL1-11-040 | Start Date*: 2009-09-14 | |||||||||||
Sponsor Name:NPS Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Investigate the Use of NPSP 558, a Recombinant Human Parathyroid Hormone [rhPTH(1-84)] for the Treatment of Adults with Hypoparathyr... | |||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DK (Completed) BE (Completed) GB (Completed) IT (Completed) LT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020081-22 | Sponsor Protocol Number: R&D 2185 | Start Date*: 2011-02-08 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: The administration of Parathyroid hormone affects functional recovery from pertrochanteric fractured neck of femur: A prospective randomised comparative pilot study with blinded objective functiona... | ||
Medical condition: Osteoporotic or low energy pertrochanteric hip fractures | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001890-26 | Sponsor Protocol Number: TRACTOR | Start Date*: 2014-05-06 | |||||||||||
Sponsor Name:Dipartimento di Medicina e Chirurgia Traslazionale dell’Università degli Studi di Firenze | |||||||||||||
Full Title: Recombinant human parathyroid hormone [rh PTH(1-34): Teriparatide] as therapy for refractory hypoparathyroidism | |||||||||||||
Medical condition: Refractory hypoparathyroidism | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004465-32 | Sponsor Protocol Number: 2011/386 | Start Date*: 2011-12-12 | |||||||||||
Sponsor Name:Dept. of Cardiothoracic & Vascular Surgery, Aarhus University Hospital, Skejby | |||||||||||||
Full Title: Can post-operative treatment with parathyroid hormone enhance bone healing and quality of newly formed bone after sternotomy in cardiac surgery patients? | |||||||||||||
Medical condition: Sternotomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000606-36 | Sponsor Protocol Number: 84421383 | Start Date*: 2008-04-07 | |||||||||||
Sponsor Name:Aarhus University Hospital, Dept of Endocrinology and Metabolism C | |||||||||||||
Full Title: Treatment of hypoparathyroidism with subcutaneous PTH (1-84) injections: effects on muscle function and quality of life | |||||||||||||
Medical condition: Hypoparathyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004316-73 | Sponsor Protocol Number: 3189 | Start Date*: 2006-08-23 |
Sponsor Name:Royal Liverpool University hospital | ||
Full Title: The effects of growth hormone, strontium ranelate and phosphate on PTH circadian rhythm, PTH target organ sensitivity, bone turnover markers, phospho-calcium metabolism and bone mineral density. A ... | ||
Medical condition: Osteoporosis and Reduced Bone mineral density (T scores< -1.0 on DEXA scan), Adult growth hormone deficiency ( GH levels,9mU/l on Insulin stress test) with reduced BMD (T scores< -1.0 on DEXA scan) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005683-21 | Sponsor Protocol Number: ENM-EA-030 | Start Date*: 2012-10-09 |
Sponsor Name:Medizinische Universität Graz | ||
Full Title: Effects of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Primary hyperparathyroidism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000640-10 | Sponsor Protocol Number: GPR-II-18-1 | Start Date*: 2019-10-10 | ||||||||||||||||
Sponsor Name:LABORATOIRES SMB S.A. | ||||||||||||||||||
Full Title: A phase II, randomised, double-blind, and parallel study to estimate the dose-response of vitamin D supplementation in chronic kidney disease patients with secondary hyperparathyroidism and vitamin... | ||||||||||||||||||
Medical condition: chronic kidney disease, stage 3 with secondary hyperparathyroidism and vitamin D deficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011883-12 | Sponsor Protocol Number: I2Y-MC-GHFA(c) | Start Date*: 2009-08-26 | |||||||||||
Sponsor Name:Elli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Study for Transdermal Application of Teriparatide | |||||||||||||
Medical condition: Treatment of osteoporosis in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005374-57 | Sponsor Protocol Number: Calcimimetics | Start Date*: 2013-02-15 | |||||||||||
Sponsor Name:Department of Breast and Endocrine Surgery, Karolinska University Hospital | |||||||||||||
Full Title: Primary hyperparathyroidism: Short-term calcimimetics treatment – Relevance for parathyroid surgery decisions? | |||||||||||||
Medical condition: Primary hyperparathyroidism (PHPT) is a common disease, characterized by a high-normal calcium concentration and an inappropriately increased parathyroid hormone (PTH) level | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004136-30 | Sponsor Protocol Number: 20130213 | Start Date*: 2014-03-05 | ||||||||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc. (a subsidiary of Amgen, Inc.) | ||||||||||||||||||
Full Title: A Multicenter Single-arm Extension Study to Describe the Long-term Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease on Hemodialysis | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism in subjects with chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) IT (Completed) BE (Completed) AT (Completed) ES (Completed) PT (Completed) LT (Completed) PL (Completed) CZ (Completed) DK (Completed) LV (Completed) DE (Completed) GR (Completed) HU (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002610-13 | Sponsor Protocol Number: M11-612 | Start Date*: 2013-12-06 |
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
Full Title: A Phase 3, Open-Label, Multicenter Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects Ages 10 to 16 with Stage 5 Chronic Kidney Disease Receiving Peritoneal Dialysis or Hem... | ||
Medical condition: - Stage 5 chronic kidney disease - Secondary to hyperparathyroidism | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: PT (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000178-24 | Sponsor Protocol Number: W2021.040 | Start Date*: 2023-10-20 |
Sponsor Name: | ||
Full Title: Active vitamin D for secondary hyperparathyroidism after bariatric surgery: a multicenter randomized controlled trial. | ||
Medical condition: patients with secondary hyperparathyroidism after Roux-en-Y gastric bypass surgery (RYGB). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002808-41 | Sponsor Protocol Number: 20120231(KAI-4169-008) | Start Date*: 2013-01-22 | ||||||||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc. (a subsidiary of Amgen, Inc.) | ||||||||||||||||||
Full Title: A Multicenter Single-arm Extension Study to Describe the Long-term Efficacy and Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease on Hemod... | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism in subjects with chronic kidney disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BE (Completed) CZ (Completed) GB (Completed) SE (Completed) ES (Completed) IT (Completed) AT (Completed) PL (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
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