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

  • Corporate

    The Lancet publishes Chiesi's TRILOGY COPD study

    The Lancet publishes the results of Chiesi Farmaceutici TRILOGY study, which shows one year data on the superior efficacy of the first extrafine fixed ICS/LABA/LAMA triple combination for COPD treatment compared with standard therapy. The results of the study provide convincing support for the…

  • Corporate

    Chiesi's extrafine triple combination benefits COPD patients

    Chiesi is the first Company to complete 2 multicenter long-term clinical studies with an extrafine fixed triple combination for COPD The preliminary results of the two 12-month studies demonstrate that Chiesi extrafine fixed triple combination improves lung function, reduces exacerbations and…

  • Corporate

    Extrafine ICS/LABA cuts COPD exacerbations

    In the treatment of chronic obstructive pulmonary disease (COPD) the combination of inhaled corticosteroids (ICS) and long acting bronchodilators LABA (Long Acting Beta2-agonists) reduces moderate and severe exacerbations, and it is recommended for this purpose in the in-force clinical guidelines. A…

  • Corporate

    Chiesi to acquire three hospital products

    Chiesi USA, Inc. and Chiesi Farmaceutici S.p.A., Chiesi USA's parent company, announced today that the companies have agreed to acquire worldwide rights of The Medicines Company to Kengreal® (cangrelor) and Cleviprex® (clevidipine), as well as rights to Argatroban for Injection, 50 mg per 50 mL. All…

  • Corporate

    80 years of Chiesi: strong international growth in 2015

    Chiesi Farmaceutici generated just under €1.5bn in revenue in 2015, a year-on-year increase of almost 10%. The international footprint of the Group continues to grow: 80% of turnover is now from the non-Italian market. The expansion of Chiesi’s US affiliate is extremely promising, as is the Group’s…

  • Corporate

    Europe approves Holoclar, the first stem-cell medicine

    The European Commission has granted a conditional marketing authorization, under Regulation (EC) No 726/2004, to Holoclar ®, an advanced therapy based on autologous stem cells and capable to restore the eyesight of patients with severe cornea damage. Holoclar ® is manufactured by Holostem Terapie…

  • Corporate

    Chiesi's extra-fine inhaler for persistent asthma

    The first extra-fine dry powder inhaler was successfully launched in Italy on October 2013 to address the unmet doctors’ and patients’ need of a user-friendly and safe drug delivery device. Being an high quality alternative to the pressurised metered dose inhaler, this innovative device can deliver…