Leerink Global Healthcare Conference 2026
Logotype for Natera Inc

Natera (NTRA) Leerink Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Natera Inc

Leerink Global Healthcare Conference 2026 summary

11 Mar, 2026

Growth and performance highlights

  • Signatera has experienced significant volume growth, reaching 22,500 growth units last quarter and 225,000 units overall, with a recommended focus on trailing four quarters average to account for seasonality and compounding effects.

  • Average selling price (ASP) for Signatera is currently $1,225, with potential to reach $2,000 as coverage expands and the test becomes standard of care, following trends seen in NIPT and Oncotype DX.

  • Medicare broadly reimburses Signatera, while commercial payer coverage is still expanding, impacting realized ASP.

  • Women's health business maintains over 40% market share in NIPT, with strong reimbursement and ongoing improvements in realized pricing.

  • Operating expenses are projected to grow 9.5% this year, with SG&A roughly flat, reflecting operating leverage.

Clinical evidence and R&D priorities

  • Continuous publication of compelling data across tumor types, with recent strong results in head and neck cancer at ASCO GU.

  • Major R&D investment ($800 million, up 30% YoY) is focused on Signatera clinical trials, new product development in women's health, and early cancer detection, especially colorectal cancer.

  • The FIND study for colorectal cancer screening is actively enrolling, representing a significant investment based on strong preliminary data.

  • Foresight acquisition enhances Signatera's sensitivity through phased and structural variants, with analytic validity already demonstrated and clinical outcomes data to be integrated over time.

  • Product development and clinical trial efforts span the portfolio, with Signatera as the central focus.

Regulatory and market expansion

  • FDA approval for Signatera as a companion diagnostic (CDx) for atezolizumab in muscle-invasive bladder cancer is expected this year, following positive IMvigor011 phase III results.

  • FDA approval could drive incremental demand and further establish Signatera as standard of care in MRD and recurrence monitoring.

  • Hospital systems are beginning to implement IMvigor011 protocols, increasing adoption.

  • Expansion into rare disease newborn testing leverages technological and commercial adjacencies from existing products.

  • Early cancer detection in colorectal cancer is seen as a distinct, large market, with plasma-based tests addressing unmet needs for millions who avoid colonoscopy.

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