NOVARTIS ALFONSO DE ANGOITIA AND BERNARDO GOMEZ

Novartis to Acquire Avidity Biosciences for $12 Billion to Boost Rare-Disease Portfolio

Key Highlights

  • Deal Value: $12 billion all-cash purchase
  • Premium: 46 % above Avidity’s previous close
  • Avidity Ticker: NASDAQ : RNA
  • Lead Drug: Del-zota for Duchenne muscular dystrophy variant
  • Spin-Off: Early-stage cardiology assets to form new public company Spinco
  • Strategic Fit: Strengthens Novartis’s U.S. presence and rare-disease portfolio
  • Comparable Moves: Kate Therapeutics ($ Nov 2024 ), Anthos Therapeutics ($ 3.1 billion ), Regulus Therapeutics ($ 1.7 billion ), Matchpoint Therapeutics partnership ($ 1 billion +)

Introduction: A Bold Bet on Rare-Disease Innovation

In a decisive move to deepen its rare-disease pipeline, Novartis AG (NOVN.S) announced plans to acquire Avidity Biosciences Inc. for approximately $12 billion in cash.

Under the agreement, Avidity shareholders will receive $72 per share, reflecting a 46 % premium to Friday’s closing price. The deal underscores Novartis’s determination to offset patent-expiry risks by expanding into high-growth therapeutic niches such as rare mscle disorders.

Deal Structure: Cash Buyout and Spin-Off

According to both companies, Avidity will spin out its early-stage cardiology programs into a separate entity called Spinco, which will become an independent publicly traded company.

Spinco will be led by Kathleen Gallagher, Avidity’s current chief program officer, ensuring continuity in R&D efforts that fall outside Novartis’s immediate focus.

This dual-track structure enables Novartis to integrate Avidity’s advanced RNA-delivery platform while allowing early exploratory programs to grow autonomously.

Strategic Rationale: Strengthening the Rare-Disease Pipeline

The acquisition expands Novartis’s reach in rare muscle and neuromuscular disorders—areas with limited existing therapies and high unmet need.

Avidity’s lead candidate, Del-zota, targets a rare subtype of Duchenne muscular dystrophy (DMD) and is currently in early-to-mid-stage clinical development. Two additional pipeline drugs address severe muscle diseases, with approval filings expected by 2026.

These therapies use proprietary RNA-delivery technology designed to deliver genetic material directly into muscle tissue—a platform that could complement Novartis’s established expertise in gene and cell therapies.

Navigating the U.S. Market Amid Trade Uncertainty

The acquisition also bolsters Novartis’s strategic position in the United States, the world’s largest pharmaceutical market, where the company faces potential policy headwinds.

Following U.S. President Donald Trump’s new tariff regime, which included 39 % tariffs on Swiss exports before exempting pharmaceuticals, global drugmakers such as Johnson & Johnson, Roche, and Sanofi have pledged new U.S. investments.

By purchasing a California-based biotech, Novartis not only mitigates trade-risk exposure but also strengthens its domestic R&D footprint — a move analysts view as both defensive and opportunistic.

Consistent Deal Momentum: Novartis’s M&A Strategy

The Avidity deal is the latest in a string of acquisitions positioning Novartis as a leader in precision-medicine markets:

  • Kate Therapeutics (Nov 2024): Gene-therapy developer for neuromuscular diseases
  • Anthos Therapeutics (Feb 2025): $3.1 billion cardiovascular-drug acquisition
  • Regulus Therapeutics (Apr 2025): $1.7 billion kidney-disorder therapy deal
  • Matchpoint Therapeutics (Jul 2025): Partnership worth up to $1 billion in oral inflammatory-disease drugs

This steady deal flow reflects Novartis’s “pipeline-through-partnership” model, enabling access to innovative biotech assets without overextending internal R&D resources.

Analyst Reaction: Managing the Patent Cliff

Industry analysts view the Avidity buyout as a strategic hedge against looming patent expirations for blockbuster drugs such as Entresto, Xolair, and Cosentyx.

“Novartis is clearly preparing for its post-patent era,” said a healthcare analyst at Zurich-based Vontobel Bank. “Avidity’s RNA-based platform offers long-term growth potential in markets that remain largely untapped.”

The deal also signals confidence that rare-disease therapies, though niche, can deliver high-margin, sustainable revenue as payers increasingly reward innovation in unmet-need categories.

Conclusion: Novartis Bets on RNA Medicine and U.S. Expansion

The $12 billion Avidity Biosciences acquisition reinforces Novartis’s transformation into a leaner, innovation-driven pharmaceutical powerhouse.

By combining Avidity’s cutting-edge RNA-delivery technology with its global development infrastructure, Novartis is positioning itself at the forefront of next-generation rare-disease therapeutics.

As the Swiss pharma group continues to recalibrate its portfolio ahead of major patent expiries and regulatory shifts, this acquisition may mark a pivotal moment in its U.S. growth strategy and RNA-therapy leadership.


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