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

  • Corporate

    Chiesi selects Salesforce Agentforce Life Sciences

    International biopharmaceutical leader accelerates digital transformation with AI-powered customer engagement, unified data, and next-generation integration capabilities APRIL 20, 2026 – Chiesi Group, an international biopharmaceutical group, has selected Salesforce’s Agentforce Life Sciences for…

  • Innovation

    Positive CHMP opinion for paediatric LOJUXTA in HoFH

    Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion, with European Commission (EC) decision anticipated by June 1, 2026 If approved, this would expand the indication of lomitapide to include children 5 years of age and older with HoFH PARMA, Italy – March 30, 2026 –…

  • Innovation

    EC approves four-weekly dosing for Elfabrio

    Approved dosing regimen reduces the burden for eligible patients, their families, and the broader healthcare system by extending infusion interval from every-two-weeks to every-four-weeks for those stable with an enzyme replacement therapy (ERT) With this decision, announced ahead of Fabry Disease…

  • Corporate

    Chiesi and Bespak partner on UK inhaler production

    Highlights Agreement builds on existing Chiesi-Bespak collaboration, reinforcing a trusted relationship as Chiesi works to evolve a portfolio of extrafine formulation Carbon Minimal Inhalers [1], ensuring patients retain continuity of care while reducing carbon emissions Bespak’s leadership in…

  • Innovation

    Positive CHMP opinion for four-weekly Elfabrio in the EU

    Committee for Medicinal Products for Human Use (CHMP) issues a positive opinion following re-examination, which will be reviewed by the European Commission (EC), with a decision anticipated by March 2026 If approved by the EC, this dosing regimen would reduce the burden to eligible patients, their…

  • Innovation

    Chiesi's Carbon Minimal Inhaler data at the BTS meeting

    Key Highlights The two studies presented at BTS demonstrated therapeutic equivalence and similar safety profiles of Chiesi’s beclometasone dipropionate/ formoterol fumarate product formulated with next generation HFA-152a propellant, compared to the current HFA-134a formulation, in two different…

  • Partnership

    Chiesi licenses AbbVie's Aliada blood-brain barrier tech

    PARMA, Italy - Nov. 12, 2025 – Chiesi Group today announced it has entered into an exclusive license agreement with Aliada Therapeutics, a wholly owned subsidiary of AbbVie, to advance blood-brain barrier (BBB)-crossing platform technology in lysosomal storage disorders (LSD) to address challenging…

  • Corporate

    Chiesi expands its La Chaussee-Saint-Victor site in France

    November 4, 2025– La Chaussée-Saint-Victor (France) – Today, the biopharmaceutical group Chiesi, a major player in the treatment of respiratory diseases, inaugurated the expansion of its industrial site located in La Chaussée-Saint-Victor, near Blois, in France. For Chiesi, improving patient health…

  • Partnership

    Chiesi and Arbor partner on rare disease gene editing

    Exclusive collaboration and license agreement for the development and global commercialization of Arbor’s clinical-stage gene editing program, ABO-101 for primary hyperoxaluria type 1 (PH1) Multitarget research collaboration and option agreement for Arbor’s innovative gene editing technologies for…