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Clinical trials for Anemia

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

  • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).


    The EU Clinical Trials Register currently displays   44339   clinical trials with a EudraCT protocol, of which   7369   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
    Examples: Cancer AND drug name. Pneumonia AND sponsor name.
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    Search Tips: Under advanced search you can use filters for Country, Age Group, Gender, Trial Phase, Trial Status, Date Range, Rare Diseases and Orphan Designation. For these items you should use the filters and not add them to your search terms in the text field.
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    Query did not match any clinical trials.
    These are paediatric studies completed by 26 January 2007, in respect of products authorised in the Community (Article 45 of the Paediatric Regulation (EC) No 1901/2006).
    Note: Advanced search filters for country, trial phase, gender, rare disease, IMP with orphan designation in the indication and age ranges of in-utero, adult or elderly do not apply to these records.
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    Study title: EFFECTS OF TREATMENT WITH ALBENDAZOLE ON GROWTH, ANEMIA AND PHYSICAL FITNESS IN KENYAN PRIMARY SCHOOL CHILDREN WITH HOOKWORM TRICHURIS AND ASCARIS INFECTIONS
    Active substance: ALBENDAZOLE
    Study summary document link (including results):
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    Document reference: 46323
    Study title: Kokil-S. Anemia in dermatitis seborrheica and the curative effect of biotin. Annales paediatrici. International review of pediatrics, {Ann-Paediatr}, Feb 1956, vol. 186, no. 2, p. 79-82, ISSN: 0365-4966.Kokil-S. Anemia in dermatitis seborrheica and the curative effect of biotin. Annales paediatrici. International review of pediatrics, {Ann-Paediatr}, Feb 1956, vol. 186, no. 2, p. 79-82, ISSN: 0365-4966.
    Active substance: BIOTIN
    Study summary document link (including results):
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    Document reference: 22589
    Study title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Weekly PROCRIT (Epoetin Alfa) on Anemia and Quality of Life in Children With Cancer Undergoing Myelosuppressive Chemotherapy
    Active substance: ERYTHROPOIETIN
    Study summary document link (including results): PR99-11-034_Interventional_Epoetin alfa.xls
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    Document reference: 26583
    Study title: Correcton of renal anemia with recombinant human erythropoietin (rhEPO) ameliorates growth in children with preterminal renal failure (PTRF) P-238 Müller-Weifel et. al.: [Abstract]. (In: 9th Congress of the International Pediatric Nephrology Association) Pediatr Nephrol 1992;6(5):C170 P-149
    Active substance: ERYTHROPOIETIN
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    Document reference: 26579
    Study title: Correcton of renal anemia with recombinant human erythropoietin (rhEPO) ameliorates growth in children with preterminal renal failure (PTRF) P-238 Müller-Weifel et. al.: [Abstract]. (In: 9th Congress of the International Pediatric Nephrology Association) Pediatr Nephrol 1992;6(5):C170
    Active substance: ERYTHROPOIETIN
    Study summary document link (including results): shannon1992_eprex.pdf
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    Document reference: 26586
    Study title: Double-Blind, Placebo-Controlled, Study to Determine Safety and Efficacy of R-HuEPO in the Anemia of Prematurity
    Active substance: ERYTHROPOIETIN
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    Document reference: 26582
    Study title: Placebo-Controlled, Double-Blind, Dose-ranging Study of the Safety and Efficacy of recombinant human Erythropoietin (R-HUEPO) in the Prophylaxis and Treatment of the Anemia of Prematurity
    Active substance: ERYTHROPOIETIN
    Study summary document link (including results): CC 2574-P129_Interventional_Epoetin alfa.xls
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    Document reference: 26581
    Study title: Recombinant human Erythropoietin (R-HUEPO) in the Anemia of Prematurity: A Multi-Center Double-Blind, Placebo-Controlled, Study
    Active substance: ERYTHROPOIETIN
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    Document reference: 26584
    Study title: Recombinant human Erythropoietin (R-HUEPO) in the Anemia of Prematurity: A Multi-Center Double-Blind, Placebo-Controlled, Study
    Active substance: ERYTHROPOIETIN
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    Document reference: 26585
    Study title: CLINICAL USEFULNESS OF DIFLUCAN FOR SYSTEMIC MYCOSIS ASSOCIATED WITH HEMATOLOGICAL ANEMIA IN GRANULOCYTOPENIC PEDIATRIC PATIENTS.
    Active substance: FLUCONAZOLE
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    Document reference: 27507
    Study title: CLINICAL USEFULNESS OF DIFLUCAN FOR SYSTEMIC MYCOSIS ASSOCIATED WITH HEMATOLOGICAL ANEMIA IN GRANULOCYTOPENIC PEDIATRIC PATIENTS.
    Active substance: FLUCONAZOLE
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    Document reference: 27871
    Study title: Kojima, S., Hibi, S., Kosaka, Y., et al. Immunosuppressive therapy using antithymocyte globulin, cyclosporine, and danazol with or without human granulocyte colony-Stimulating factor in children with acquired aplastic anemia Blood 96(6): 2049-2054.Kojima, S., Hibi, S., Kosaka, Y., et al. Immunosuppressive therapy using antithymocyte globulin, cyclosporine, and danazol with or without human granulocyte colony-Stimulating factor in children with acquired aplastic anemia Blood 96(6): 2049-2054.
    Active substance: FILGASTRIM
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    Document reference: 27278
    Study title: Godo A et al: Comparison of efficacy and tolerability netween iton protein succinylate and iron sulphate - Study in 80 patients with iron deficiency anemia. General Pediatric Service, University Hospital Center, Tirana, Albania.
    Active substance: FERRIC PROTEINSUCCINYLATE
    Study summary document link (including results):
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    Document reference: 27208
    Study title: Mandich Z & Angebrandt S: Clinical trial - Iron protein succinylate (Legofer) in threatment of anemia. Pediatric Clinic, Clinical Hospital, Osijek, Croatia.
    Active substance: FERRIC PROTEINSUCCINYLATE
    Study summary document link (including results):
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    Document reference: 27206
    Study title: Markova G: Hypochromic anemia in the breast-feeding age (Treatment with Legofer). Healt Care center Lisiche, Skopje, Macedonia
    Active substance: FERRIC PROTEINSUCCINYLATE
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    Document reference: 27203
    Study title: Nakich M et al: Legofer in the treatment of sideropenic anemia in children with a solid tumor. Pediatrics Clinic Zagreb, Croatia
    Active substance: FERRIC PROTEINSUCCINYLATE
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    Document reference: 27207
    Study title: Smokvina M: Trivalen iron-protein succinylat (Legofer) in treatment of sideropenic anemia in children. Hematologic - Onkologic clinical care unit, Pediatrics clinic, Rijeka, Croatia.
    Active substance: FERRIC PROTEINSUCCINYLATE
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    Document reference: 27204
    Study title: Mamula, P. et al. Total Dose Intravenous Infusion of Iron Dextran for Iron-Deficiency Anemia in Children With Inflammatory Bowel Disease, Journal of Pediatric Gastroenterology and Nutrition (2002) 34:286-290.
    Active substance: FERRIC OXIDE DEXTRAN COMPLEX
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    Document reference: 27195
    Study title: Peck, S.N. et al. Safety and efficacy of iron dextran infusions in children with inflammatory bowel disease and iron deficiency anemia, Journal of Pediatric Gastroenterology and Nutrition (1998) 27: 487.
    Active substance: FERRIC OXIDE DEXTRAN COMPLEX
    Study summary document link (including results):
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    Document reference: 27196
    Study title: Atanasova B et al: The results of application of recombinant eritropoetin for prevention of anemia (cases) of prematurely borne in department of neonatology in University Hospital Pleven. Department of Neonatology, University Hospital- Pleven & House of Medical and social care – Pleven, Bulgaria
    Active substance: FERRIC PROTEINSUCCINYLATE
    Study summary document link (including results):
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    Document reference: 27199
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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