Initiating coverage of Netherlands-based Pharming, analysts at Edison Investment Research say that the company's Rhucin, recombinant human C1 esterase inhibitor, is now under European Union regulatory review and could receive approval in the second half of this year. It could be EU partnered in the first half and a US launch is possible in 2011.
Rhucin has potential in transplantation (possible Phase II studies in 2010 with direct sales possible by 2014-15) and use in cardiac surgery could be a blockbuster indication. In January, 7.5 million euros ($10.7 million) of convertible bonds plus 15 million warrants at 0.5 euros were issued giving convertible debt of 18.4 million euros. Liquid cash was 12.3 million euros; a 23.4 million-euro equity facility underpins the fiscal year 2010 cash-burn, the analysts note.
A leading EU position in hereditary angioedema
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