Australian infectious disease therapy and vaccine development company BioDiem Ltd (ASX: BDM) today announced positive results from formal studies of its BDM-E eye disease drug, presented over 21 – 22 July at the International Society for Eye Research (ISER) meeting in Berlin, Germany. The ISER convenes leading researchers and clinicians in the area of eye disease.
BDM-E has received Orphan Drug designation from the United States Food & Drug Administration (FDA) for the treatment of the inherited degenerative eye disorder, retinitis pigmentosa (RP).
The eye research results presented at the ISER Conference confirm the potential of BDM-E:
- BDM-E was found to reduce formation of abnormal blood vessel growth;
- BDM-E was found to reduce the signs of damage typical to retinitis pigmentosa; and
- BDM-E was shown to improve the function of the retina and inhibit the death of cells imperative for sight.
BioDiem recently signed a research agreement with the Foundation Fighting Blindness, a leading US eye research advocate, to test BDM-E in a pre-clinical model of RP, a genetic cause of blindness without effective treatment options.
The Australian research into BDM-E being presented in Berlin was conducted under retinal disease specialist Professor Jennifer Wilkinson-Berka from Monash University, a Senior Research Fellow of the National Health and Medical Research Council (NHMRC) of Australia, and Associate Professor Erica Fletcher from The University of Melbourne.
The encouraging results add further momentum to BioDiem’s plan to out-license the BDM-E technology. “These results contribute to the strong and growing preclinical evidence showing BDM-E‘s positive effect in models of eye disease, and will help progress out-licensing opportunities for the drug.” said BioDiem Chief Executive Officer Julie Phillips.
The scientific poster demonstrating the results of the BDM-E studies may be found at www.biodiem.com.
About BioDiem Ltd
BioDiem is an ASX-listed company based in Melbourne with an international focus on discovering, developing and commercialising world-class research and technology targeting cancers and infectious diseases. BioDiem’s core technologies include the Live Attenuated Influenza Virus (LAIV), the SAVINE platform and the BDM-I antimicrobial compound.
The LAIV influenza vaccine is an intranasal vaccine to prevent infection from seasonal and pandemic influenza. The LAIV influenza vaccine can be produced using both egg-based and cell-based manufacturing methods. The cell-based LAIV vaccine has completed a Phase II clinical trial in Europe. The egg-based LAIV vaccine technology is licensed to the World Health Organization as part of the Global Pandemic Influenza Action Plan to Increase Vaccine Supply.
The LAIV influenza vaccine is marketed as Nasovac™ in India by the Serum Institute of India, and has been licensed to China-based Changchun BCHT Biotechnology Co. The LAIV vaccine was in-licensed from the Institute of Experimental Medicine in St Petersburg, Russia where it has been used for over a decade in many millions of people - children, adults and the elderly. The LAIV is administered by nasal spray and induces a rapid immune response in the mucosal lining of the nose and pharynx.