Alnylam Pursues Value Framework To Accelerate Givlaari Access In EU
Following Approval Of The RNAi Therapeutic By The European Commission
Executive Summary
Alnylam’s short-interfering RNA, Givlaari, has become the first treatment to be approved for preventing attacks of acute hepatic porphyria in the EU, and Alnylam wants to pursue a value-based agreement framework to accelerate patient and provider access.
You may also be interested in...
For An Ultra-High-Priced Drug, Alnylam Brings A New Idea
The company will launch Givlaari with a novel prevalence-based adjustment feature for payers, which will trigger higher rebates if the number of diagnosed patients is higher than expected.
Alnylam Wins FDA Approval For Givlaari, Its Second RNAi Drug
Givosiran was approved by the US FDA for the treatment of acute hepatic porphyria, a rare generic blood disorder, nearly three months ahead of the action date.
Boehringer Ingelheim Boosts COVID-19 Efforts As Jardiance Continues To Impress
Germany’s family-owned Boehringer Ingelheim has supplemented its research efforts into finding COVID-19 therapies by supporting employees who volunteer to take part in COVID-19 relief efforts and by donating health care supplies, helped by a solid 2019 financial performance.
Need a specific report? 1000+ reports available
Buy Reports