Drugs / Erythropoietin Beta

Trials 2 · a red edge is where a trial was stopped

20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2 NCT00551291 Aug 2007 → Jun 2009 myelodysplastic syndrome Hoffmann-La Roche Completed No outcome recorded
Phase 2 NCT00140010 Apr 2005 → Mar 2007 acquired aneurysmal subarachnoid hemorrhage University of Cambridge Completed No outcome recorded
Also used as a comparator or background therapy in 3 trials
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 21 trial
Phase 2 NCT00284271 Background Jan 2004 → Dec 2005 Hodgkins lymphoma University of Cologne Completed No outcome recorded
Phase 2/31 trial
Phase 2/3 NCT00654992 Comparator Sep 2006 → Feb 2008 acute kidney injury Seoul National University Bundang Hospital Completed No outcome recorded
Phase 31 trial
Phase 3 NCT01732146 Comparator Mar 2013 → Feb 2017 brain hypoxia - ischemia Assistance Publique - Hôpitaux de Paris Completed No outcome recorded

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as Erythropoietin Beta ClinicalTrials.gov intervention name — accepted as the source's own label NCT00551291
4

NCT00140010

NCT00654992

NCT01732146

NCT00284271

Known as Epoetin beta “This study is a randomized, double-blind, placebo-controlled clinical trial investigating the potentially beneficial effects of systemic recombinant human erythropoietin...” NCT00140010
Known as NeoRecormon “This study is a randomized, double-blind, placebo-controlled clinical trial investigating the potentially beneficial effects of systemic recombinant human erythropoietin...” NCT00140010
Action Activate “By activation of endothelial EPO receptors” NCT00140010
Modality Protein / enzyme biologic “Epoetin beta is a 165-aa glycoprotein manufactured by using recombinant DNA technology” NCT00140010
Route Intravenous “30,000 units in 6 mL of 0.9% saline IV for 15 minutes every other day for 3 doses within 72 hours after aneurysmal subarachnoid hemorrhage” NCT00140010