A reminder3 Sep 2013 04:00
Xenetic Biosciences expects higher rating from US switch
By Giles Gwinnett July 17 2013, 1:35pm
Xenetic Biosciences (LON:XEN) is finally embarking on the process of "serious value" growth, according to its chief executive.
This week Xenetic announced it is searching for a suitable candidate to reverse into to get a US listing, while the company’s own development programmes for potential blockbuster drugs for western markets also starts soon.
Chief executive Scott Maguire recently colourfully compared this process as being like a "battleship leaving the dock".
He's referring to the first western clinical trial of ErepoXen for treating chronic anaemia, which is starting in Australia at the end of this month or next - one of several drugs in the firm's portfolio and a candidate that the firm wholly controls.
Maguire explains that previously Xenetic has been purely research-based, relying on out-licensing partnerships and collaborations with groups in India and Russia.
But, following a fundraising last year, the company has now begun the process of evolving into a drug developer, able to test and commercialise its own products.
Maguire is so excited about this transition because, not only does if offer potentially large rewards for shareholders, but also because the firm's portfolio itself is highly promising.
Xenetic specialises in developing orphan drugs for rare diseases, which have multi-billion dollar potential. Orphan drugs are fast-tracked to the market because they typically address diseases and conditions for which there are few, if any, medications.
Now, following the firm's undeniable progress thus far, what is needed, is delivering on plans and, of course, securing financing, reckons Maguire.
"As I see it, as management, the science is working and it's going to come down to a function of execution and money to deliver on the promise, because it's clear that these products we have in development have blockbuster potential and those are not my words, those are words from the investment and strategic community," he said.
And Maguire highlighted all three of its technological platforms - PolyXen, ImuXen, OncoHist - have products in at least phase 2 clinical trials.
Currently, its main focus is ErepoXen - the firm's most advanced product and likely to be the key share driver. Ironically, perhaps, this drug is one that does not fit into the firm's orphan strategy, in that it is a big, mass-market candidate.
Maguire says the plan is to complete a dose finding study for western markets in December this year before striking a deal.
"The goal of ErepoXen is to out-license as soon as allowable and there is already some interest in this product," he adds.
"This is a big market drug, very expensive clinical trials, so we are going to be seeking a partner to out-license this as soon as we have data coming out of Australia/New Zealand.