- Trials with a EudraCT protocol (14,811)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (59)
14,811 result(s) found for: Secondary.
Displaying page 1 of 741.
EudraCT Number: 2007-006645-41 | Sponsor Protocol Number: SLAZ-Heuvel | Start Date*: 2008-06-13 | |||||||||||
Sponsor Name:Sint Lucas Andreas Hospital | |||||||||||||
Full Title: The (cost)effectiveness of paricalcitol in the treatment of secondary hyperparathyroidism in hemodialysis patients. | |||||||||||||
Medical condition: Secondary hyperparathyroidism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021041-42 | Sponsor Protocol Number: 25051954 | Start Date*: 2011-01-28 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Use of Calcimimetics vs oral Paricalcitol in Renal transplant Patients affected with Persistent Secondary Hyperparathyroidism. A pilot study | |||||||||||||
Medical condition: Renal transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007017-76 | Sponsor Protocol Number: 01PTHi | Start Date*: 2009-03-24 | |||||||||||
Sponsor Name:Josep M Cruzado | |||||||||||||
Full Title: Estudio prospectivo, randomizado para comparar paratiroidectomía subtotal versus cinacalcet en el tratamiento del hiperparatiroidismo secundario persistente post trasplante renal. | |||||||||||||
Medical condition: Hiperparatiroidismo secundario post trasplante renal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005051-28 | Sponsor Protocol Number: 20140336 | Start Date*: 2016-08-22 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-label, Single-dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Etelcalcetide (AMG 416) in Paediatric Subjects Aged 2 to less than 18 Years with Sec... | |||||||||||||
Medical condition: Secondary Hyperparathyroidism (sHPT) Receiving Maintenance Haemodialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) LT (Completed) GB (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004958-18 | Sponsor Protocol Number: 20130356 | Start Date*: 2014-07-14 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: A Randomized, Open-label, Controlled Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis | |||||||||||||
Medical condition: Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SK (Completed) IT (Completed) HU (Completed) ES (Completed) BE (Completed) CZ (Completed) PT (Completed) DE (Completed) Outside EU/EEA GR (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002075-40 | Sponsor Protocol Number: 20050182 | Start Date*: 2006-10-04 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: EVOLVE - Evaluation Of Cinacalcet HCl Therapy to Lower Cardiovascular Events | |||||||||||||
Medical condition: Secondary hyperparathyroidism (HPT) in subjects with chronic kidney disease (CKD) receiving maintenance hemodialysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) NL (Completed) AT (Completed) DE (Completed) IE (Completed) BE (Completed) PT (Completed) DK (Completed) GB (Completed) HU (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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: 2009-011378-14 | Sponsor Protocol Number: M10-967 | Start Date*: 2009-11-03 | ||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | ||||||||||||||||||
Full Title: The IMPACT SHPT Study: Study to Evaluate the Improved Management of iPTH with Paricalcitol-centered Therapy vs. Cinacalcet Therapy with Low-dose Vitamin D in Hemodialysis Patients with Secondary H... | ||||||||||||||||||
Medical condition: Secondary hyperparathyroidism (SHPT) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) NL (Completed) ES (Completed) PT (Completed) GB (Completed) SE (Completed) IT (Completed) GR (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003056-36 | Sponsor Protocol Number: CBAF312A2304 | Start Date*: 2012-10-31 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel-group, placebo-controlled variable treatment duration study evaluating the efficacy and safety of Siponimod (BAF312) in patients with secondary pro... | |||||||||||||
Medical condition: Secondary progressive multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) IE (Completed) DE (Prematurely Ended) CZ (Completed) SK (Completed) NL (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) AT (Completed) SE (Completed) PT (Prematurely Ended) IT (Prematurely Ended) LV (Completed) GR (Completed) LT (Completed) EE (Completed) BE (Prematurely Ended) PL (Completed) BG (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
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 |
EudraCT Number: 2007-001043-22 | Sponsor Protocol Number: HECT01206 | Start Date*: 2007-11-21 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: A Multicenter, Open-Label Study of Hectorol (doxercalciferol capsules) for the Treatment of Secondary Hyperparathyroidism in Stage 3 or Stage 4 Chronic Kidney Disease (CKD) Patients | |||||||||||||
Medical condition: Secondary hyperparathyroidism in Stage 3 or Stage 4 Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006380-36 | Sponsor Protocol Number: APPLE | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A PROSPECTIVE, PILOT, CROSS-OVER STUDY TO ASSESS THE EFFICACY OF PARICALCITOL IN REDUCING PARATHYROID HORMONE LEVELS AND AMELIORATING MARKERS OF BONE REMODELLING IN RENAL TRANSPLANT RECIPIENTS WITH... | |||||||||||||
Medical condition: Persistent secondary hyperparathyroidism in renal transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004436-36 | Sponsor Protocol Number: Rituximab1.5 | Start Date*: 2013-04-19 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: A prospective pilotstudy of immunological and radiological effects of intrathecal rituximab in patients with secondary progressive multiple sclerosis | |||||||||||||
Medical condition: Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
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: 2009-017999-25 | Sponsor Protocol Number: 20090005 | Start Date*: 2010-11-12 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: An Open-Label, Single-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Cinacalcet HCl in Pediatric Subjects Aged 28 Days to < 6 Years with Chronic Kidney Di... | |||||||||||||
Medical condition: Secondary hyperparathyroidism (HPT) in subjects with chronic kidney disease (CKD) receiving maintenance hemodialysis. | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005981-37 | Sponsor Protocol Number: 8. udgave; 6. september 2006 | Start Date*: 2006-12-20 | |||||||||||
Sponsor Name:Roskilde Amts Sygehus | |||||||||||||
Full Title: Behandling af sekundær hyperparathyreoidisme hos uræmiske patienter. En sammenlignenede undersøgelse mellem virkningen af alfacalcidol og paricalcitol. | |||||||||||||
Medical condition: Secondary hyperparathyroidism is a common feature in patients with chronic kidney disease. Reduced synthesis of active vitamin D contributes to secondary hyperparathyroidism. Therefore we primaril... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004411-22 | Sponsor Protocol Number: CSPP100A2365E2 | Start Date*: 2012-03-14 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A multicenter, 52 to 104 week extension study to evaluate the long term growth and development of pediatric hypertensive patients 6 – 17 years of age treated previously with aliskiren | ||||||||||||||||||
Medical condition: Hypertension | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA SK (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004618-40 | Sponsor Protocol Number: 20110100 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An Open-label, Single-arm Study to Assess the Safety and Tolerability of Cinacalcet HCl in Addition to Standard of Care in Pediatric Subjects Age 28 Days to < 6 Years with Chronic Kidney Disease an... | |||||||||||||
Medical condition: Secondary hyperparathyroidism in pediatric subjects with chronic kidney disease receiving hemodialysis or peritoneal dialysis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Temporarily Halted) PL (Completed) HU (Completed) CZ (Completed) IT (Completed) SK (Completed) BE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003563-38 | Sponsor Protocol Number: 20140159 | Start Date*: 2015-04-21 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: A Multicenter Single-arm Extension Study to Characterize the Long-term Safety of Cinacalcet Hydrochloride in the Treatment of Secondary Hyperparathyroidism in Pediatric Subjects With Chronic Kidn... | |||||||||||||
Medical condition: Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) HU (Completed) CZ (Completed) ES (Completed) BE (Completed) SK (Completed) FR (Completed) Outside EU/EEA GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002659-28 | Sponsor Protocol Number: 20160428 | Start Date*: 2017-11-10 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: An open-label, Randomized, Single-dose, 2-Period, "-Treatment Crossover Study to Assess the Bioequivalence of Cinacalcet Capsule (Administered as Six of the 5 mg Cinacalcet Capsules) with 30 mg Com... | |||||||||||||
Medical condition: Secondary hyperparathyroidism in patients with chronic kidney disease on dialysis and for the treatment of hypercalcemia in patients with parathyroid carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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