Canaccord Genuity's 46th Annual Growth Conference
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Natera (NTRA) Canaccord Genuity's 46th Annual Growth Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Natera Inc

Canaccord Genuity's 46th Annual Growth Conference summary

13 Aug, 2026

Financial and operational performance

  • Achieved record Q2 results with strong volume growth across all business segments, especially in organ health and women's health, despite seasonal headwinds.

  • Women's health saw high single-digit year-over-year growth, driven by uptake of Fetal Focus and a new, more sensitive Panorama version for NIPT.

  • Oncology segment posted a record 283,000 clinical units for Signatera, with sequential growth of 34,000 units, partly due to weather-related Q1 delays.

  • Gross margins remained strong, losses narrowed, and aggressive investment continued, positioning the business for sustained growth.

  • Revenue guidance was raised, reflecting momentum and a significant re-rating of expectations for the year.

Product innovation and clinical data

  • Launched a more sensitive Panorama version for NIPT, with strong performance in low fetal fraction cases and upcoming publications.

  • Ongoing improvements to Signatera, including phased variant detection, are expected to further differentiate the offering.

  • Extensive outcomes data and prospective studies underpin product leadership, with many studies set to read out between 2026 and 2029.

  • Recent FDA approval for Signatera in muscle-invasive bladder cancer (MIBC) and inclusion in NCCN guidelines are expected to drive further adoption.

  • Additional FDA approvals are anticipated as more trials are conducted in other cancer types.

Market access, reimbursement, and global expansion

  • Medicare coverage now includes most common tumor types; ongoing submissions target less common cancers, with positive engagement from MolDX.

  • ASP for Signatera is $1,275, with potential $150–$200 upside from new indications; Japan approval for CRC achieved, with bladder cancer submission underway and launch targeted for early 2027.

  • European expansion is underway following IVDR approval, with demand driven by national health systems seeking cost-effective, targeted therapies.

  • Market sizing is approached country by country, focusing on reimbursable use cases and local needs.

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