Swiss pharmaceutical company Novartis Pharma AG (SIX:NOVN) (NYSE:NVS) announced on Tuesday that it has signed an agreement to acquire Anthos Therapeutics, a clinical-stage biopharmaceutical company, for an upfront payment of USD925m.
This acquisition adds abelacimab, a late-stage monoclonal antibody targeting Factor XI inhibition, to Novartis' cardiovascular pipeline.
Abelacimab is in Phase 3 trials for preventing stroke and systemic embolism in patients with atrial fibrillation, as well as cancer-associated thrombosis. The drug has received Fast Track Designation from the US Food and Drug Administration (FDA) for both indications.
Anthos Therapeutics was founded in 2019 by Blackstone Life Sciences and Novartis, with abelacimab developed under a licence from Novartis. Phase 2 data showed the drug significantly reduced bleeding events compared to standard anticoagulants.
The agreement includes potential milestone payments of up to USD2.15bn based on regulatory and sales achievements.
Subject to customary conditions, the transaction is expected to close in the first half of 2025.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval