Ionis announces that FDA accepts New Drug Application and grants Priority Review of tofersen for a rare, genetic form of ALSPRNewsWire • 07/26/22
Ionis announces enrollment completion of Phase 3 Lp(a) HORIZON cardiovascular outcomes study of pelacarsenPRNewsWire • 07/20/22
Ionis to participate in virtual fireside chat at H.C. Wainwright 1st Annual Hereditary Angioedema ConferencePRNewsWire • 07/13/22
Ionis partner licenses rare kidney disease treatment and will advance into Phase 3 clinical studyPRNewsWire • 07/11/22
Ionis announces presentation of positive Phase 2b data for chronic hepatitis B treatment at the EASL International Liver Congress™PRNewsWire • 06/25/22
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