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Novartis to Acquire Anthos Therapeutics for $925M, Advancing Novel Stroke Prevention Drug Abelacimab

• Novartis has entered into an agreement to acquire Anthos Therapeutics for $925 million upfront, with potential additional payments of up to $2.15 billion based on milestone achievements.

• Abelacimab, a first-in-class Factor XI inhibitor antibody, demonstrated significant reduction in bleeding events compared to standard anticoagulants in Phase 2 trials for atrial fibrillation patients.

• The acquisition strengthens Novartis's cardiovascular portfolio with a late-stage asset that has received FDA Fast Track Designation for both cancer-associated thrombosis and stroke prevention in atrial fibrillation.

Novartis announced today its plans to acquire Boston-based Anthos Therapeutics for $925 million upfront, marking a significant expansion of its cardiovascular pipeline. The acquisition centers on abelacimab, a potential first-in-class monoclonal antibody targeting Factor XI inhibition for stroke prevention and thrombosis treatment.

Strategic Acquisition Details

The deal includes potential additional payments of up to $2.15 billion tied to regulatory and sales milestones, with the transaction expected to close in the first half of 2025. This move represents a homecoming for abelacimab, which originated at Novartis before being licensed to Anthos Therapeutics when it was launched in 2019 through a collaboration with Blackstone Life Sciences.

Promising Clinical Development Program

Abelacimab has shown compelling results in clinical trials, particularly in its Phase 2 AZALEA study. The trial demonstrated a significant reduction in bleeding events compared to standard direct-oral anticoagulants in atrial fibrillation patients. The drug's development program currently includes three ongoing Phase 3 trials:
  • LILAC-TIMI 76: Focusing on stroke prevention in atrial fibrillation
  • ASTER: Evaluating treatment of cancer-associated thrombosis
  • MAGNOLIA: Investigating treatment of gastrointestinal/genitourinary cancer-associated thrombosis

Innovative Mechanism of Action

Abelacimab represents a novel approach to anticoagulation through its selective targeting of Factor XI. The drug is designed as a fully human monoclonal antibody that blocks Factor XI activation, mimicking natural Factor XI deficiency – a condition associated with protection from thromboembolic disease while maintaining effective hemostasis.

Regulatory Recognition

The FDA has acknowledged abelacimab's potential by granting Fast Track Designation for two indications:
  • Treatment of cancer-associated thrombosis (July 2022)
  • Prevention of stroke and systemic embolism in atrial fibrillation patients (September 2022)
"We are excited to join forces to advance the development of abelacimab, a potential first-in-class treatment and safer approach for stroke prevention in atrial fibrillation as well as cancer-associated thrombosis," said Shreeram Aradhye, M.D., President, Development and Chief Medical Officer at Novartis.

Market Impact and Strategic Fit

The acquisition aligns with Novartis's strategic focus on cardiovascular medicine, complementing their existing portfolio of treatments for heart disease. David Soergel, M.D., Global Head of Cardiovascular, Renal and Metabolism Development Unit at Novartis, emphasized the strategic timing: "Now is the right time to bring abelacimab back into the Novartis CRM pipeline."
This transaction strengthens Novartis's position in the cardiovascular space while potentially offering patients a safer alternative to current anticoagulation therapies. The development of abelacimab could represent a significant advance in the management of thrombotic conditions, particularly for patients at high risk of bleeding complications.
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