- Trials with a EudraCT protocol (23)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
23 result(s) found for: Hypochromic anemia.
Displaying page 1 of 2.
EudraCT Number: 2009-017409-13 | Sponsor Protocol Number: MD2009.04 | Start Date*: 2010-06-30 | |||||||||||||||||||||
Sponsor Name:Sanquin Plasma Products | |||||||||||||||||||||||
Full Title: Dose escalating study to evaluate pharmacokinetics, efficacy and safety of apotransferrin in atransferrinemia patients. Estudio de escalada de dosis para evaluar la farmacocinÊtica, la eficacia y l... | |||||||||||||||||||||||
Medical condition: Atransferrinemia | |||||||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004979-13 | Sponsor Protocol Number: 2012-496 | Start Date*: 2014-01-29 | ||||||||||||||||
Sponsor Name:Rigshospitalet, 2032 | ||||||||||||||||||
Full Title: Treatment of Preoperative Anaemia in Patients with Urogenital Cancer: A Randomised Double-Blind Placebo-Controlled Study of Intravenous Iron Isomaltide 1000 Monofer© versus Saline | ||||||||||||||||||
Medical condition: Iron deficiency anaemia and anaemia of chronic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002380-27 | Sponsor Protocol Number: ML21040 | Start Date*: 2007-09-05 | |||||||||||
Sponsor Name:Roche s.r.o. | |||||||||||||
Full Title: A single arm open label study to assess the efficacy, safety and tolerability and of once-monthly administration of intravenous C.E.R.A. for the maintanance of haemoglobin levels in dialysis patien... | |||||||||||||
Medical condition: Chronic renal anaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003679-37 | Sponsor Protocol Number: ML21349 | Start Date*: 2007-09-04 | |||||||||||
Sponsor Name:Roche a/s | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety, and tolerability of once-monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin levels in haemodialysis p... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007758-70 | Sponsor Protocol Number: NH19707 | Start Date*: 2008-06-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: An open-label multi-center, multiple dose study to determine the optimum starting dose of intravenous MIRCERA® for maintenance treatment of anemia in pediatric patients with chronic kidney disease ... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease in pediatric patients (CKD) on hemodialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) FR (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000081-13 | Sponsor Protocol Number: BA 17284 | Start Date*: 2004-09-07 |
Sponsor Name:F Hoffmann-La Roche Ltd | ||
Full Title: A randomized, controlled, open-label, multi-center, parallel group study to demonstrate efficacy and safety of RO0503821 when administered with pre-filled syringes for the maintenance treatment of ... | ||
Medical condition: Patients with Chronic Kidney Disease who are on dialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005799-15 | Sponsor Protocol Number: ML21438 | Start Date*: 2008-04-08 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety and tolerability of once-monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin levels in haemodialysis pati... | |||||||||||||
Medical condition: Chronic renal anemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002032-26 | Sponsor Protocol Number: BH 18387 | Start Date*: 2004-12-23 |
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||
Full Title: An open-label, multi-center study to document the efficacy, safety and tolerability of long-term administration of RO0503821 in patients with chronic renal anemia | ||
Medical condition: Patient with chronic renal anaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) FI (Completed) HU (Completed) DK (Completed) SE (Completed) CZ (Completed) NO (Completed) IT (Completed) DE (Completed) AT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004510-33 | Sponsor Protocol Number: BH17847 | Start Date*: 2006-11-15 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized, controlled, open-label, multi-center, parallel-group study to compare the efficacy and safety of RO0503821 with that of darbepoetin alfa administered intravenously at extended dosing ... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) AT (Completed) FI (Completed) BE (Completed) PT (Completed) NL (Completed) DK (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006349-15 | Sponsor Protocol Number: ML20952 | Start Date*: 2007-09-11 | |||||||||||
Sponsor Name:Roche (HELLAS) SA | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety and tolerability of once- monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin levels in dyalysis patients... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003955-35 | Sponsor Protocol Number: MH21299 | Start Date*: 2007-10-24 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A controlled open label randomised parallel group study to evaluate the efficacy, safety, and tolerability of subcutaneous MIRCERA, versus no ESA therapy, in the treatment of anaemia in CKD patient... | |||||||||||||
Medical condition: post renal transplant anaemia patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Prematurely Ended) BE (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006523-40 | Sponsor Protocol Number: ML20944 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Roche AB | |||||||||||||
Full Title: A single arm open label study to assess the efficacy, safety and tolerability and of once-monthly administration of subcutaneous C.E.R.A. for the maintenance of haemoglobin levels in pre-dialysis p... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005528-34 | Sponsor Protocol Number: ML21348 | Start Date*: 2008-02-22 | |||||||||||
Sponsor Name:N.V. Roche S.A. | |||||||||||||
Full Title: Subcutaneous Treatment of Anemia in patients with a GFR Below 45 ml/min/1.73m2 through Injections with Mircera as low frequent as Once monthly | |||||||||||||
Medical condition: Chronic renal anaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005621-28 | Sponsor Protocol Number: ML20752 | Start Date*: 2008-02-22 | |||||||||||
Sponsor Name:Roche (Hungary) Ltd | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety and tolerability of once-monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin levels in dialysis patients ... | |||||||||||||
Medical condition: To assess the long term maintenance of haemoglobin levels, with once-monthly intravenous administration of C.E.R.A. in dialysis patients with chronic renal anaemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001434-41 | Sponsor Protocol Number: NH20052 | Start Date*: 2006-11-27 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: An open-label, randomized, multicenter, parallel group study to demonstrate correction of anemia using once every four week subcutaneous injections of RO0503821 in patients with chronic kidney dise... | |||||||||||||
Medical condition: Chronic renal anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) SE (Prematurely Ended) GR (Completed) IT (Completed) BE (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003173-40 | Sponsor Protocol Number: ML21439 | Start Date*: 2008-07-01 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A single arm, open label study to assess the efficacy, safety and tolerability of once-monthly administration of subcutaneous C.E.R.A. for the maintenance of haemoglobin levels in pre-dialysis pati... | |||||||||||||
Medical condition: Chronic renal anaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004552-21 | Sponsor Protocol Number: BH20051 | Start Date*: 2007-02-21 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: An open-label, randomized, multi-center, parallel group non-inferiority study of subcutaneous injections of RO0503821 given once monthly vs. darbepoetin alfa given according to local label in pati... | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) GB (Completed) IT (Completed) BE (Completed) CZ (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020401-32 | Sponsor Protocol Number: darbepoetina | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: IDENTIFICATION OF OXIDATIVE-STRESS AND MICROINFLAMMATION GENES MODULATED BY ERYTHROPOIETIN ADMINISTRATION IN PATIENTS WITH RENAL TRANSPLANT AND CHRONIC RENAL FAILURE. PERSPECTIVES FOR ERYTHROPOITIN... | |||||||||||||
Medical condition: PATIENTS WITH RENAL TRANSPLANT AND CHRONIC RENAL FAILURE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001721-97 | Sponsor Protocol Number: ML20826 | Start Date*: 2007-10-15 |
Sponsor Name:Roche Pharma (Schweiz) AG | ||
Full Title: An single arm, open label, interventional multicenter study to assess the efficacy, safety and tolerability of once-monthly administration of intravenous C.E.R.A. for the maintenance of haemoglobin... | ||
Medical condition: chronic renal anemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-004050-29 | Sponsor Protocol Number: PHI116581 | Start Date*: 2013-01-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A four-week Phase IIa, randomized, double-blind, placebocontrolled, parallel-group, multi-center study to evaluate the safety, efficacy and pharmacokinetics of GSK1278863 in subjects with anemia as... | |||||||||||||
Medical condition: Anemia associated with chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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