Alnylam Pharma (ALNY) Confirms Approval of GIVLAARI by FDA
FREE Breaking News Alerts from StreetInsider.com!
StreetInsider.com Top Tickers, 9/25/2026
- S&P 500 ends marginally lower as investors focus on US-Iran war
- Oracle triggers force majeure on massive 'Project Jupiter' data center
- Oil gains on little sign of progress in US-Iran talks
- S&P 500 history shows strong gains across Fed hiking cycles: BCA
- JPMorgan upgrades CoreWeave on stronger compute pricing
- Bloom Energy falls as Oracle invokes force majeure on AI project
- Akamai signs $11.6B deal with Anthropic, up to $20B potential
- Oracle triggers force majeure on massive 'Project Jupiter' data center
- Oracle Sends Force Majeure Notice Over New Mexico Data Center - Bloomberg
- US and Iran discuss phased deal to reopen Hormuz and end US blockade, sources say
Alnylam Announces Approval of GIVLAARI™ (givosiran) by the U.S. Food and Drug Administration (FDA)
November 20, 2019 2:03 PM ESTGIVLAARI Approved for the Treatment of Adults with Acute Hepatic Porphyria (AHP) Based on ENVISION Phase 3 Study Results Showing Significant Reduction in the Rate of Porphyria Attacks in Patients with AHP
FDA Approval Received in Less Than Four Months after New Drug Application (NDA) Filing Acceptance
GIVLAARI Becomes Second RNAi Therapeutic from Alnylam Approved by FDA in Last 16 Months and First-Ever Approval for a GalNAc-Conjugate RNA Therapeutic, a Landmark in Advancement of Precision Genetic Medicines
Alnylam to Host Conference Call Today at 2:15 p.m. ET
... More
