Ionis partner Roche shows Phase 3 data for sefaxersen in IgAN
Sifaxersen reduced proteinuria by 43.1% relative to placebo at 37 weeks. The investigational therapy inhibits complement factor B and is well tolerated in the IMAgINATION study.
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RNA- and DNA-targeted medicines developer
ionis.comLast updated
In short: Ionis secured FDA approvals for TRYNGOLZA and Zanvastro but faced cardio trial setbacks in 2026.
Sifaxersen reduced proteinuria by 43.1% relative to placebo at 37 weeks. The investigational therapy inhibits complement factor B and is well tolerated in the IMAgINATION study.
Bepirovirsen treats chronic hepatitis B with unprecedented functional cure rates. Ionis licensed the drug to GSK and earns milestone payments and royalties.
The EMA committee recommends approval for treating severe hypertriglyceridemia. Final EC decision is expected in Q4 2026.
Partner Roche's IMAgINATION study met primary endpoints. Interim results show significant proteinuria reduction with a favorable safety profile.
Hibsago is viewed as a potential "functional cure" for chronic infections and an important part of the British drugmaker's goal of reaching £40 billion in...
Ionis on Friday said the recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use covers Tryngolza as an adjunct to diet...
A late-stage test of Roche and Ionis Pharmaceuticals’ sefaxersen showed that the drug reduced protein in the urine, which ...
Otsuka Pharmaceutical and Ionis Pharmaceuticals said on Tuesday their experimental drug met the main goal of a late-stage study in patients with a rare inherited...
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