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Chiesi Group receives European Marketing Authorization for Trimbow® inhalation powder

Published: Apr 21, 2021 Chronic obstructive pulmonary disease (COPD) patients for whom a dry powder inhaler device is preferred, can now benefit from an extrafine formulation fixed triple combination therapy containing an inhaled corticosteroid (ICS) / long-acting β2-agonist (LABA) / long-acting muscarinic antagonist (LAMA) in a single device. With this new European authorization, Chiesi reinforces its commitment to providing a broad portfolio of formulations and devices to COPD patients. PARMA, Italy, April 21, 2021 (GLOBE NEWSWIRE) Chiesi, an international research-focused healthcare group (Chiesi Group), today announced that the European Commission has granted the marketing authorization for Trimbow® inhalation powder delivered through NEXThaler (beclometasone dipropionate, formoterol fumarate dihydrate and glycopyrronium), an extrafine formulation triple fixed combination therapy in a single dry powder inhaler (DPI), for the maintenance treatment in adult patients wit

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