AstraZeneca, Ionis plan to seek FDA approval for rare-disease therapy this yearMarket Watch • 06/21/22
Ionis announces eplontersen met co-primary and secondary endpoints in interim analysis of the Phase 3 NEURO-TTRansform study for hereditary transthyretin-mediated amyloid polyneuropathy (ATTRv-PN)PRNewsWire • 06/21/22
Ionis treatment for Angelman syndrome receives orphan drug and rare pediatric disease designations from U.S. FDAPRNewsWire • 06/13/22
Ionis partner Biogen announces that results from Phase 3 VALOR study and open-label extension of tofersen showed clinical benefit in SOD1-ALS patientsPRNewsWire • 06/03/22
Ionis Pharmaceuticals, Inc. (IONS) CEO Brett Monia on Q1 2022 Results - Earnings Call TranscriptSeeking Alpha • 05/04/22
Ionis announces positive data for ETESIAN Phase 2b study of antisense medicine targeting PCSK9 at 2022 American College of Cardiology Scientific SessionPRNewsWire • 04/04/22
Biogen (BIIB), Ionis to End Early-Stage ALS Candidate DevelopmentZacks Investment Research • 03/29/22
Biogen and Ionis Announce Topline Phase 1 Study Results of Investigational Drug in C9orf72 Amyotrophic Lateral SclerosisPRNewsWire • 03/28/22
Ionis announces publication of positive Phase 2 data for donidalorsen in New England Journal of MedicinePRNewsWire • 03/16/22
Ionis calls for applications for Janice Wiesman Young Investigator Grant ProgramPRNewsWire • 03/07/22