We are pleased to see the MOLBREEVI BLA filed, following its resubmission. Addionally , we are encouraged to see Priority Review granted (no real surprise), with PDUFA date set for 8/22/26. As we connue to believe the data package robustly demonstrates MOLBREEVI's efficacy and safety for the treatment of autoimmune PAP (aPAP), we expect approval. As a reminder, MOLBREEVI has already been granted FTD, BTD, ODD (FDA/EMA), and Innovaon Passport (IP) and Promising Innovave Medicine (PIM) by UK's MHRA. SVRA plans to submit MOLBREEVI Markeng Authorizaon Applicaon (MAAs) for aPAP to the EMA and MHRA by end of 1Q26. Based on the strength of the data, and our recent KOL checks - which emphasized the potenal usage of MOLBREEVI across all paents (mild, moderate and severe) - we believe MOLBREEVI is well-posioned for commercial success.