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BioWorld - Friday, March 6, 2026
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Home » Wilson shares climb as it embarks on pivotal phase III trial for rare genetic condition
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Wilson shares climb as it embarks on pivotal phase III trial for rare genetic condition

Oct. 24, 2017
By Michael Fitzhugh
Sweden's Wilson Therapeutics AB said that the first patient in a single pivotal trial of its copper-protein-binding agent for the rare copper-excess condition, Wilson disease, is expected to be enrolled in early 2018. Data from the study is anticipated to follow in the second half of 2019.
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