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For all press and media enquiries please contact mediarelations@chiesi.com 

  • Corporate

    FDA approves PRX-102 (pegunigalsidase alfa) for Fabry

    - Following the recent European Commission Authorization, FDA approves PRX-102 for the treatment of Fabry disease - PARMA, BOSTON and CARMIEL, Israel, May 10, 2023 – Chiesi Global Rare Diseases, a business unit of the Chiesi Group established to deliver innovative therapies and solutions for people…

  • Corporate

    EC authorises PRX-102 (pegunigalsidase alfa) for Fabry

    - PEGylated enzyme replacement therapy designed to provide a long half-life - PARMA, Italy, BOSTON and CARMIEL, Israel, May 5 th, 2023 – Chiesi Global Rare Diseases, a business unit of the Chiesi Group established to deliver innovative therapies and solutions for people affected by rare diseases,…

  • Corporate

    Chiesi completes the Amryt Pharma acquisition

    Acquisition positions Chiesi to expand patient access to approved treatments and advance efforts to develop new treatments for people living with rare diseases. Parma Italy, Dublin Ireland and Boston MA, April 12, 2023 – Chiesi Farmaceutici S.p.A. (“Chiesi”), an international, research-focused…

  • Corporate

    2022: Chiesi's international growth continues

    Turnover at €2 billion 749 million, with growth of 13.6% over 2021; The European market remains at the center, with significant international development; The distribution of turnover by therapeutic area is as follows: Air (respiratory diseases) 73%, Rare (rare and ultra-rare diseases) 12% and Care…

  • Partnership

    Chiesi and Affibody collaborate on respiratory drugs

    Chiesi Group and Affibody will collaborate closely to develop novel Affibody ® molecules as innovative treatments for respiratory diseases. This agreement expands Chiesi’s comprehensive R&D program in respiratory diseases with high unmet medical needs. Affibody will receive an upfront payment,…

  • Corporate

    Chiesi launches the Restore to Impact call for ideas

    International Call for ideas for the regeneration of the Chiesi pharmaceutical group's historic industrial site at Via Palermo, Parma March 1 st – April 30 th, 2023 Starting today, Wednesday 1 March, Restore to Impact - The next healthcare landmark for innovation and future-oriented competences, an…

  • Innovation

    Positive CHMP opinion for pegunigalsidase alfa in Fabry

    - European Commission decision anticipated in beginning of May 2023 - PARMA, Italy and BOSTON and CARMIEL, Israel, February 24 th, 2023 – Chiesi Global Rare Diseases, a business unit of the Chiesi Group established to deliver innovative therapies and solutions for people affected by rare diseases,…

  • Innovation

    Chiesi presents Fabry data at WORLDSymposium 2023

    Company also presents insights from the SPARKLE registry in alpha-mannosidosis that highlight a delay in diagnosis, identify the most frequent genetic MAN2B1 variant in enrolled participants, and report on real-world clinical profiles. BOSTON, February 24, 2023 – Chiesi Global Rare Diseases, a…

  • Innovation

    FDA approves Lamzede for alpha-mannosidosis

    First and only enzyme replacement therapy for the treatment of non-central nervous system manifestations of alpha-mannosidosis in adult and pediatric patients; Ultra-rare progressive disease presents with wide range of symptoms. BOSTON, February 20, 2023 – Chiesi Global Rare Diseases, a business…