Rockwell Medical (Nasdaq:RMTI), a fully-integrated biopharmaceutical company offering innovative products and services targeting end-stage renal disease (ESRD), chronic kidney disease (CKD), and iron deficiency anemia, announced today that Phase IIb data for its lead drug candidate Soluble Ferric Pyrophosphate (SFP) have been accepted for presentation at the XLVII European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress, organized in collaboration with the Deutsche Gesellschaft fur Nephrologie (DGfN) in Munich, Germany, June 25-28, 2010.
The SFP Phase IIb data were submitted as a late-breaking clinical trial abstract. The acceptance of the abstract for the meeting is noteworthy, as only significant clinical trials of extraordinary importance are considered for presentation.
Phase IIb data will be presented during the ERA-EDTA meeting for Rockwell's investigational drug SFP, which is being studied as an iron replacement product for maintaining hemoglobin in the target range while reducing erythropoiesis stimulating agent (ESA) dosage in adult hemodialysis-dependent chronic kidney disease (CKD-HD) patients. The data will be presented in the poster area of the International Congress Centre Munich on June 26, 2010, number Sa681. Dr. Ajay Gupta, Chief Scientific Officer, and Dr. Richard Yocum, VP of Drug Development, will be present throughout the two official poster sessions from 10:30 to 11:15 hrs. and from 16:15 to 17:00 hrs.
"We are looking forward to sharing this SFP data at the ERA-EDTA meeting in June," stated Dr. Richard Yocum, VP of Clinical Development at Rockwell. "We are focused on bringing SFP, a novel continuous iron maintenance therapy, to the worldwide ESRD patient population. After our upcoming meeting with the FDA, we hope to initiate our Phase III clinical program in the second-half of this year."
GLP-1 receptor agonists reduce kidney failure risk and cardiovascular events