Overview
- CSL agreed to pay $117 million upfront for an exclusive option to acquire VarmX, exercisable after reviewing Phase 3 results for VMX-C001.
- CSL will fully finance the global Phase III EquilibriX-S study in patients on Factor Xa direct oral anticoagulants who need urgent surgery, and will cover manufacturing and other pre-launch work.
- VarmX shareholders could receive up to $388 million in additional payments before a potential launch and as much as $1.7 billion tied to sales milestones if the drug reaches the market.
- VMX-C001 is intended as a single-dose reversal for anticoagulants such as Eliquis and Xarelto, with a non-thrombogenic safety profile viewed as critical after concerns with Andexxa.
- The companies cite FDA fast track status and an anticipated 2029 commercial timeline, contingent on positive Phase 3 data, option exercise, and regulatory approvals.