Showing posts with label Orphan Drug Application. Show all posts
Showing posts with label Orphan Drug Application. Show all posts

EMEA granted Oxabact Orphan Drug Designation for Treatment of Short Bowel Syndrome...

HEADLINE2OxThera AB announced today that its product Oxabactœ has been granted an Orphan Drug Designation in the European Union for treatment of Short Bowel Syndrome.
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.
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.  

TGA Guidance for Orphan Drug Application...

Guidance on orphan drug designation has been published as part of an ongoing initiative to provide our stakeholders with a clear understanding of Australia's regulatory requirements for therapeutic goods.

This was progressed as part of the TGA reforms: A Blueprint for TGA's future.

The Blueprint aims to improve the Australian community's understanding of our regulatory processes and decisions, and to enhance public trust in the safety and quality of therapeutic goods. As part of this, we are working to ensure that the regulatory guidance available to potential applicants is accessible, comprehensive, easily understood, and available in different formats to meet their needs.

'Orphan drugs' are often developed to treat small and very specific patient populations who suffer from rare diseases and conditions.
The application and evaluation fees for orphan drugs can be waived to:
  • help reduce their development costs
  • facilitate their access to the Australian marketplace
However, a medicine needs to be:
  • designated by us as an orphan drug before an application can be accepted to register it on the Australian Register of Therapeutic Goods (ARTG)
  • evaluated for quality, safety and efficacy in the same way as other registered medicines.
GUIDELINES AVAILABLE CLICK HERE