|
Click here to view online. Add this email to your safelist. |
|||||||||||
|
|
|||||||||||
|
Update on US regulatory review of PT010 in COPD |
|||||||||||
|
|
|||||||||||
|
1 October 2019
AstraZeneca today announced that the US Food and Drug Administration (FDA) has issued a complete response letter regarding the New Drug Application (NDA) for PT010 (budesonide/glycopyrronium/ formoterol fumarate), an inhaled triple-combination therapy and potential new medicine for patients with chronic obstructive pulmonary disease (COPD). |
|||||||||||
|