OxThera, Inc. Release: Oxabact® Granted European Medicines Agency Orphan Drug Designation For Treatment Of SBS
STOCKHOLM, September 23, 2014 /PRNewswire via COMTEX/ -- STOCKHOLM, September 23, 2014 /PRNewswire/ --
SBS is a highly disabling malabsorptive condition. SBS is associated with significant morbidity and mortality, reduced quality of life and high healthcare costs.
"We are happy to announce that Oxabact® is now also recognized as a potential treatment for Short Bowel Syndrome. OxThera believe that Oxabact® would be an excellent add-on therapy in SBS patients and would help the underlying gastritis and malabsorption in the gut, as well as subsequently reducing plasma oxalate and preventing kidney disease," said Elisabeth Lindner, CEO of OxThera.
EMA/Committee on Orphan Medicinal Products (COMP) considered that OxThera had provided data from preclinical models and preliminary clinical data, suggesting favourable effects of Oxabact® in SBS. The Committee considered that this may translate into clinically relevant benefit for patients affected by the condition.
Oxabact® is an oral product composed of highly concentrated live bacteria (Oxalobacter formigenes). OxThera is currently pursuing a complete clinical development program in the EU and in the US for the treatment of patients suffering from Primary Hyperoxaluria.
Oxabact® previously holds orphan drug designations in the EU and the US for the treatment of Primary Hyperoxaluria.
About Short Bowel Syndrome
Short Bowel Syndrome is an intestinal failure and is characterised by diarrhoea, nutrient malabsorption, bowel dilation and dysmobility. The mean prevalence is estimated at about 0.39 in 10,000 in the European population, translating to almost 20,000 patients. Approximately 15,000 people in the US have Short Bowel Syndrome.
About Secondary Hyperoxaluria
Secondary Hyperoxaluria results from excess intake, malabsorption or malsecretion of oxalate. The disorder may cause recurrent kidney stones. An estimated four million people in the US suffer from kidney stone disease.
About Primary Hyperoxaluria
Primary Hyperoxaluria is a rare inborn autosomal genetic disorder leading to markedly elevated levels of endogenous oxalate in plasma and urine. High levels of urinary oxalate cause kidney damage, including recurrent kidney stone formation and/or calcification of the kidney.
OxThera holds worldwide rights for compositions and methods of use for treatment of hyperoxaluria. OxThera currently has two products in its pipeline: Oxabact® for the treatment of Primary Hyperoxaluria, and Oxazyme®, for the prevention of oxalate malabsorption and recurring kidney stones in Secondary Hyperoxaluria. OxThera operates through the head office in Stockholm, Sweden, and its subsidiary OxThera Inc. in Alachua, Florida, USA.
For further information, please contact
Elisabeth Lindner, CEO of OxThera AB, Phone +46-8-660-02-23 / +46-705934199
SOURCE OxThera AB
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