Alnylam: Positive Topline Results in Phase 3 Study of Patisiran in ATTR Amyloidosis

  Patisiran Met the Primary Endpoint with a Statistically Significant Improvement in 6-Minute Walk Test Compared to Placebo at 12 Months –

– Patisiran Also Met the First Secondary Endpoint with a Statistically Significant Improvement in Quality of Life, as Measured by the Kansas City Cardiomyopathy Questionnaire, Compared to Placebo at 12 Months –

– Patisiran Demonstrated Encouraging Safety and Tolerability Profile in Patients with ATTR Amyloidosis with Cardiomyopathy –

– Company Plans to File a Supplemental New Drug Application in U.S. in Late 2022 –

– Full Data Will Be Presented at the 18th International Symposium on Amyloidosis –

– Alnylam to Host Conference Call Today at 8:00 am ET –

Management will discuss the APOLLO-B topline results via conference call on Wednesday, August 3, 2022, at 8:00 am ET. To access the call, please register online at https://register.vevent.com/register/BI6ac74b5406af42c5980ba67c6f9e419d. Participants are requested to register at a minimum 15 minutes before the start of the call. A replay of the call will be available two hours after the call and archived on the same web page for six months.

A live audio webcast of the call will be available on the Investors section of the Company’s website at www.alnylam.com/events. An archived webcast will be available on the Company’s website approximately two hours after the event.

https://finance.yahoo.com/news/alnylam-reports-positive-topline-results-110000527.html