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Ionis presents long-term DAWNZERA data at ACAAI meeting
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Ionis presents new data demonstrating long-term disease control with DAWNZERA™ (donidalorsen) at ACAAI 2025 Annual Meeting
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Ionis reports third quarter 2025 financial results and highlights progress on key programs
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Detailed data from the landmark CORE and CORE2 pivotal studies of olezarsen for sHTG to be presented as a late breaker at AHA Scientific Sessions
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Ionis ranked #2 Top Employer by Science magazine, recognizing industry-leading scientific innovation and company culture
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Ionis CEO Brett P. Monia receives 2025 Lifetime Achievement Award from the Oligonucleotide Therapeutics Society
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Ionis to hold third quarter 2025 financial results webcast
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Ionis hosts innovation day, targets sustained cash flow by 2028
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Ionis showcases transformational medicines and industry-leading pipeline at Innovation Day
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Ionis reports positive results for Alexander disease drug zilganersen
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Ionis announces positive topline results from pivotal study of zilganersen in Alexander disease
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TRYNGOLZA approved in Europe for rare genetic syndrome FCS
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TRYNGOLZA® (olezarsen) approved in the European Union for familial chylomicronemia syndrome (FCS)
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Ionis expands adaptive event for neurological disease communities
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Ionis expands Surf Away+ event, marking 10 years of creating unique adaptive experiences for people with neurological diseases
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Ionis receives FDA breakthrough therapy designation for ION582
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Ionis receives U.S. FDA Breakthrough Therapy designation for ION582 in Angelman syndrome
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Ionis to host investors and analysts for Innovation Day 2025
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Ionis to present at upcoming investor conferences
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Ionis olezarsen shows 72% triglyceride reduction in Phase 3 studies
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Olezarsen significantly reduces triglycerides and acute pancreatitis events in landmark pivotal studies for people with severe hypertriglyceridemia (sHTG)
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DAWNZERA™ (donidalorsen) approved in the U.S. as first and only RNA-targeted prophylactic treatment for hereditary angioedema
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Ionis reports second quarter 2025 financial results and highlights progress on key programs
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Ionis drug TRYNGOLZA gets EU committee approval recommendation for rare disease
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TRYNGOLZA® (olezarsen) recommended for approval in the EU by CHMP for familial chylomicronemia syndrome (FCS)
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Ionis reports positive HAE treatment switch study results
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Phase 3 OASISplus data demonstrating benefit of donidalorsen for HAE patients who switched from other prophylactics published in JACI In Practice
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Ionis to hold second quarter 2025 financial results webcast
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Ionis Pharmaceuticals (IONS) announces Biogen to advance salanersen into SMA registrational studies based on positive interim Phase 1 results
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Ionis announces Biogen to advance salanersen into SMA registrational studies based on positive interim Phase 1 results
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Ionis Pharmaceuticals (IONS) Announces Retirement of Chief Development Officer
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Ionis announces Dr. Richard Geary, chief development officer, to retire; Dr. Holly Kordasiewicz to assume role in January 2026
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Ionis Pharmaceuticals (IONS): First patient dosed in pivotal Phase 3 REVEAL clinical study of ION582 in Angelman syndrome
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First patient dosed in pivotal Phase 3 REVEAL clinical study of ION582 in Angelman syndrome
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Ionis Pharmaceuticals (IONS) announces positive topline results from Essence study of olezarsen in people with moderately elevated triglycerides
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Ionis announces positive topline results from Essence study of olezarsen in people with moderately elevated triglycerides
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Ionis to host 2025 virtual Annual Meeting of Stockholders
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Ionis reports first quarter 2025 financial results
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New Harris Poll findings reveal HAE patients are unsatisfied with current prophylactic treatment options, with over 90% interested in trying new therapies
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Ionis to hold first quarter 2025 financial results webcast
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Ionis to host expert panel discussion on sHTG
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Ionis to present at upcoming investor conferences
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Ionis Pharmaceuticals (IONS) expands partnership with Sobi to include olezarsen commercialization outside the U.S.
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Ionis expands partnership with Sobi to include olezarsen commercialization outside the U.S.
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Ionis Pharmaceuticals (IONS) and Ono announce global license agreement
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Ionis and Ono announce global license agreement for sapablursen in polycythemia vera
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Ionis Pharmaceuticals (IONS) Announces WAINZUA approved in the EU for the treatment of hereditary transthyretin-mediated amyloidosis in adults with stage 1 or stage 2 polyneuropathy
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WAINZUA (eplontersen) approved in the EU for the treatment of hereditary transthyretin-mediated amyloidosis in adults with stage 1 or stage 2 polyneuropathy
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Ionis to present at upcoming investor conferences
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Ionis Pharmaceuticals (IONS): New positive donidalorsen data to be presented at AAAAI/WAO

