Eisai's bullish Leqembi sales projection, Takeda's Alzheimer's licensing deal and the latest on the BIOSECURE Act made our news this week.
Eisaiwing a reportedly bullish assessment Takedaedicare, Eisai has projected a significant sales increase for Leqembi. Takeda paid $100 million upfront for an option to license an anti-amyloid vaccine from AC Immune. The House Oversight Committee voted overwhelmingly to advance a tweaked version of the BIOSECURE Act. And more.
AftEisailing hitch, EisaLeqembiiogen begin rolling FDA submission for subcutaneous Leqembi
Eisai expects LeqembEisaies foBiogen2024 fiscal year will reach 56.5 billion JapaneLeqembi($364 million), compared with 4.26 billion Japanese yen ($27 million) during the 2023 fiscal year that ended in March. The company believes it and partner Biogen have improved Alzheimer’s disease diagnosis and treatment infrastructure in the U.S. and Japan. Meanwhile, after a short delay, the two companies have started a rolling FDA submission for a subcutaneous version of the anti-amyloid antibody that can be dosed at home.
FelTakedapaneseAC Immuner Takeda is also making a bet on Alzheimer’s disease, paying $100 million upfront for AC Immune’s anti-amyloid beta vaccines. One candidate in the deal, coded ACI-24.060, is in a phase 1b/2 trial in patients with prodromal Alzheimer’s or Down syndrome. The option exercise fee and milestone payments could add up to $2.1 billion.
In new letter to Defense Department, WuXi AppTec refutes claim of secret data transferWuXi AppTecWuXi Biologics
The House Committee on Oversight and WuXi AppTecity voted overwhelmingly to advance the BIOSECURE Act for a full House vote, Reuters reports. The updated version of the bill would give biopharma companies until Jan. 1, 2032, to end their existing contracts with WuXi AppTec and WuXi Biologics plus three gene sequencing firms targeted in the legislation. For potential new targets of the bill, companies would have five years to cut ties with them. Meanwhile, WuXi AppTec is also defending itself against a claim that it shared a U.S. client’s data with Beijing without consent.
Five months after theSanofiFederalShionogiommission derailPompe diseaseroposal to acquire Maze Therapeutics’ Pompe disease program, Shionogi has picked up the asset for $150 million upfront and undisclosed milestones. The candidate, MZE001, is a GYS1 inhibitor designed to stop the toxic buildup of glycogen. It has the potential to become the first oral treatment for Pompe.
ShiShionogiso suffered a setback this week. Its oCOVID-19y protease inhibitor ensitrelvir, which is approved in Japan under the brand name Xocova, failed to significantly beat placebo in reducing the time to sustained resolution of 15 common COVID-19 symptoms in a global phase 3 trial. Despite the primary endpoint miss, Shionogi noted a significant difference in the time to resolution of six COVID symptoms.
A nHengrui1 player has emerged with $400 million funding from Bain CapiBain RTW Investments, Atlas Venture and Lyra Capital plus a portfolio of three cardiometabolic candidates from Jiangsu Hengrui Pharma. Hengrui out-licensed the meds for $110 million in upfront and near-term payments, plus a 19.9% stake in the startup, called Hercules. One of the candidates is a dual GLP-1/GIP receptor agonist, the same mechanism as Eli Lilly’s tirzepatide.