Hemispherx collaborate with Emerge to seek marketing nod for Alferon N injection from Australia’s TGA & New Zealand’s Medsafe
Hemispherx Biopharma Inc, an advanced specialty pharmaceutical company, has executed an agreement with Emerge Health Pty Ltd., an innovative, specialized Australian pharmaceutical company to seek approval of Alferon N injection in Australia and New Zealand and to commence distribution of Alferon in both countries on a named-patient basis, where deemed appropriate.
Hemispherx and Emerge will collaborate on seeking regulatory approval from Australia’s Therapeutic Goods Administration (TGA) and New Zealand’s Medicines and Medical Devices Safety Authority (Medsafe).
Under an exclusive license to sell, market, and distribute Alferon N injection in Australia and New Zealand, Emerge will implement regulatory-compliant programmes to educate physicians about Alferon. Hemispherx will support these efforts and will supply Alferon at a predetermined transfer price.
Peter Davey and Chris Rossidis, co-founders of Emerge, said “Having visited Hemispherx’s upgraded Alferon manufacturing facility and met some of the company’s key people, we are impressed by what we saw and whom we met and believe that Alferon N injection represents a significant opportunity in Australia and New Zealand for patients with recurring genital warts and those refractory to recombinant interferon”.
Thomas K. Equels, executive vice chairman and CFO of Hemispherx said, “We continue to make progress toward re-launching Alferon N injection and are very pleased to be collaborating with Emerge to provide Alferon under these unique access programmes and to work with them to gain formal regulatory approval.”
Alferon N is the only natural source, multi-species alpha interferon currently approved for sale in the US. Alferon N is approved in the US only for the treatment of refractory or recurring external genital warts caused by human papilloma virus in patients 18 years of age or older.