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Orphalan announces China NMPA’s approval of its trientine tetrahydrochloride product for the treatment of Wilson disease Paris, France 18 January, 2024 - Orphalan SA (“Orphalan” or “the Company”),...
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Cuvrior™ now available in the US for the treatment of adult patients with stable Wilson disease who are de-coppered and tolerant to penicillamine — Oral administration offers dosing flexibility and...
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Orphalan announces publication of results from the CHELATE trial in The Lancet Gastroenterology & Hepatology Trial supported Orphalan’s successful application to the United States Food and Drug...
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Orphalan announces publication of results from the CHELATE trial in The Lancet Gastroenterology & Hepatology Trial supported Orphalan’s successful application to the United States Food and Drug...
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Orphalan announces enrolment of the first five patients in the International Wilson's Disease Patient Registry (“iWD Registry”) World’s first global Wilson’s Registry will provide an international...
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Orphalan announces enrolment of the first five patients in the International Wilson's Disease Patient Registry (“iWD Registry”) World’s first global Wilson’s Registry will provide an international...
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Orphalan announces data from secondary analyses of the CHELATE trial for maintenance patients with Wilson’s Disease — Data from the company’s CHELATE trial to be presented today during an oral...
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Orphalan announces FDA approval of Cuvrior™ for the treatment of adult patients with stable Wilson’s disease who are de-coppered and tolerant to penicillamine Paris, France 2 May 2022 – Orphalan SA...
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Orphalan announces FDA approval of Cuvrior™ for the treatment of adult patients with stable Wilson’s disease who are de-coppered and tolerant to penicillamine Paris, France 2 May 2022 – Orphalan SA...
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Orphalan strengthens its management team with two key appointments Paris, France 1 February 2022 – Orphalan SA, a Company that identifies, develops, and delivers therapies worldwide for orphan...