Akcea Expects Convenience Edge For Tegsedi, Despite Monitoring Requirements

Approved two months after Alnylam’s Onpattro, Tegsedi is priced almost identically in the same hATTR indication. Ionis affiliate Akcea hopes weekly subcutaneous administration will provide convenience benefit compared to I.V. Onpattro.

Sarah Boyce of Akcea
Akcea President Sarah Boyce

Akcea Therapeutics Inc. has reached the market with Tegsedi, its RNA-interference (RNAi) therapy for hereditary transthyretin-mediated amyloidosis (hATTR) related polyneuropathy, just a couple months after Alnylam Pharmaceuticals Inc. received US FDA approval for its similar drug Onpattro for the same indication. The similarities will extend to pricing, as Akcea announced it will price Tegsedi roughly on par with Onpattro.

Tegsedi (inotersen) cleared the US FDA Oct. 5 for hATTR polyneuropathy, after Alnylam’s Onpattro (patisiran) got the okay on Aug. 10 as the first drug therapy for the rare disease

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