Morgan Stanley 23rd Annual Global Healthcare Conference
Logotype for Halozyme Therapeutics Inc

Halozyme Therapeutics (HALO) Morgan Stanley 23rd Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Halozyme Therapeutics Inc

Morgan Stanley 23rd Annual Global Healthcare Conference summary

9 Jul, 2026

Business model and financial performance

  • Focus on subcutaneous drug delivery platforms, notably ENHANZE and autoinjectors, enabling rapid, high-volume biologic administration.

  • Projected 2024 revenue of $1.27–$1.335 billion, with royalty revenue expected to reach $825–$860 million, driven by Darzalex Faspro, Phesgo, and Vyvgart Hytrulo.

  • High EBITDA margins (73–75% projected for 2028) and strong free cash flow due to a leverageable, advisory-based business model with minimal R&D and commercialization costs.

  • Capital allocation prioritizes business investment, share repurchases (over $1.85 billion since 2019), and acquisitions to add new platforms.

  • Royalty streams are expected to last into the 2030s and 2040s, supporting long-term durable growth.

Market trends and growth drivers

  • Global shift toward subcutaneous therapies is accelerating, with significant adoption in China and other markets, reducing the need for hospital-based infusions.

  • Recent product launches and expanded reimbursement, especially for Phesgo in China, are fueling growth.

  • Prefilled syringe technology for Vyvgart Hytrulo has expanded prescriber base and patient access, demonstrating market expansion potential.

  • Secular trends in pharma and healthcare systems favor at-home care and easier drug administration, supporting continued portfolio expansion.

  • Four additional products launched in 2024–2025 are expected to contribute to revenue from 2026 onward.

Regulatory and policy environment

  • Positive regulatory environment with streamlined FDA approvals for subcutaneous products, enabling broader indications from single studies.

  • Ongoing engagement with CMS regarding IRA guidance; strong arguments presented for maintaining favorable classification of ENHANZE as an active ingredient.

  • Orphan drug designation changes reduce IRA impact on key products, extending their revenue timelines.

  • Final CMS guidance expected in September or October, with ongoing advocacy efforts.

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