Loading...
Loading...
Browse all stories on DeepNewz
VisitWill Alnylam's Vutrisiran (Amvuttra) receive FDA approval for ATTR cardiomyopathy by the end of 2024?
Yes • 50%
No • 50%
FDA announcements and Alnylam Pharmaceuticals press releases
Alnylam's Vutrisiran Shows Promise for ATTR Amyloidosis at European Cardiology Congress
Aug 30, 2024, 10:04 AM
Alnylam Pharmaceuticals presented detailed results from the HELIOS-B Phase 3 study of its drug Vutrisiran, also known as Amvuttra, at the European Society of Cardiology Congress. The study focused on patients with ATTR amyloidosis with cardiomyopathy. The results showed a 28% reduction in the primary composite of all-cause mortality and recurrent cardiovascular events. Additionally, there were 31% and 36% reductions in all-cause mortality during the 33-36-month double-blind period and up to month 42, respectively. Despite these positive outcomes, some endpoints, including monotherapy mortality and combination with tafamidis, were not statistically significant. Alnylam believes Amvuttra could be a first-line therapy for ATTR cardiomyopathy, though it might be more likely used as an add-on to Pfizer's Vyndamax/Vyndaqel. The company's stock, $ALNY, experienced a 2% decline, while competitor BridgeBio's stock, $BBIO, rose by 9%. The full study data supports the drug's benefit but leaves doctors with tough choices.
View original story
Approval • 33%
Conditional Approval • 33%
Rejection • 34%
Pfizer • 25%
Ionis Pharmaceuticals • 25%
Eidos Therapeutics • 25%
Other • 25%
Market leader • 33%
Second place • 33%
Third place or lower • 33%
Exceeds $1 billion in sales • 25%
Between $500 million and $1 billion in sales • 25%
Between $100 million and $500 million in sales • 25%
Less than $100 million in sales • 25%
$250 to $300 • 25%
Below $200 • 25%
Above $300 • 25%
$200 to $250 • 25%
More than 30% • 25%
20%-30% • 25%
Less than 10% • 25%
10%-20% • 25%