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OxThera: A two-for-one offer

By concentrating on two forms of a single indication for which no therapeutics are available and few are in development, OxThera AB is hoping to corner the Orphan market for primary hyperoxaluria and maintain a role in the larger secondary hyperoxaluria indication.

Primary hyperoxaluria is a rare genetic disease affecting about 2,000 patients in the U.S. and Europe, resulting

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