greeksoup/ stock research

Guardant Health, Inc.: Q2 FY2026 earnings call

What management said about Q2 FY2026, from the documents filed with the SEC on 30 July 2026: press release. Guidance figures: 7 raised, 2 kept. The quarter’s numbers.

Key takeaways

  • Revenue rose 44% year over year: Total revenue was $335.0 million, up 44% from $232.1 million, with the company citing Oncology and Screening as drivers. Source
  • Screening revenue grew over 250%: Screening revenue was $52.9 million, against $14.8 million, driven primarily by Shield screening test volume. Source
  • Oncology tests rose 63%: Oncology test volume was about 104,000 tests, an increase of 63% over the prior year period. Source
  • Shield tests reached about 66,000: Shield screening tests were about 66,000 in the quarter, against about 16,000 in the prior year period. Source
  • Non-GAAP operating expenses reached $288.3M: Non-GAAP operating expenses were $288.3 million against $215.3 million, driven by commercial infrastructure and marketing for Shield and Oncology. Source
  • Free cash flow used $69.5 million: Free cash flow was negative $69.5 million, against negative $65.9 million a year earlier; first-half free cash flow was negative $140.7 million. Source
  • Revenue guidance raised by $40 million: The company raised full-year revenue guidance by $40 million at both ends of the range, to growth of 36% to 38%. Source

“Our second-quarter performance reflected broad-based momentum across the Guardant portfolio, with revenue increasing 44% year over year,”

Helmy Eltoukhy, co-founder and co-CEO

Guidance

AreaPeriodFigureAgainst last quarter
Total revenue Sourcefull year 2026$1.34 to $1.36 billion, growth of 36% to 38%Raised from $1.30 to $1.32 billion, growth of 32% to 34%
Oncology revenue growth Sourcefull year 2026approximately 30%Raised from 28% to 29%
Oncology volume growth Sourcefull year 2026approximately 50%Raised from approximately 35%
Biopharma & Data revenue growth Sourcefull year 2026low double-digit rangeKept
Screening revenue Sourcefull year 2026$218 to $230 millionRaised from $186 to $198 million
Shield test volume Sourcefull year 2026270,000 to 285,000 testsRaised from 230,000 to 245,000 tests
Non-GAAP gross margin Sourcefull year 202664% to 65%Kept
Non-GAAP operating expenses Sourcefull year 2026$1.08 to $1.10 billionRaised from $1.05 to $1.07 billion
Free cash flow burn Sourcefull year 2026$195 million to $205 millionRaised from $185 million to $195 million

What changed from last quarter

  • Guidance raised: Full-year 2026 revenue guidance raised to $1.34 to $1.36 billion from $1.30 to $1.32 billion. Source
  • Guidance raised: Oncology revenue growth guidance raised to about 30% from 28% to 29%; oncology volume growth raised to about 50% from about 35%. Source
  • Guidance raised: Screening revenue guidance raised to $218 to $230 million from $186 to $198 million. Source
  • Guidance raised: Non-GAAP operating expense guidance raised to $1.08 to $1.10 billion from $1.05 to $1.07 billion. Source
  • Guidance raised: Free cash flow burn guidance raised to $195 to $205 million from $185 to $195 million. Source
  • Guidance kept: Non-GAAP gross margin guidance of 64% to 65% was continued from the prior release. Source
  • Guidance kept: Biopharma & Data revenue growth was continued in the low double-digit range.
  • New: Shield coverage was obtained from UnitedHealth Group, described as the first major commercial insurer to provide coverage. Source
  • New: Shield was included in the American Cancer Society's updated colorectal cancer screening guidelines. Source
  • New: FDA approval was received for Guardant360 Liquid CDx, described as the most advanced FDA-approved liquid biopsy panel. Source

Results and loss measures

  • Revenue rose 44% year over year: Total revenue was $335.0 million, up 44% from $232.1 million, with the company citing Oncology and Screening as drivers. Source
  • GAAP net loss rose to $120.1 million: Net loss was $120.1 million, or $0.90 per share, against $99.9 million, or $0.80 per share, a year earlier. Source
  • Non-GAAP loss per share was $0.42: Non-GAAP net loss was $56.2 million, or $0.42 per share, compared with $55.0 million, or $0.44 per share, a year earlier. Source
  • Adjusted EBITDA loss was $55.9 million: Adjusted EBITDA loss was $55.9 million, against $51.9 million a year earlier; stock-based compensation and related payroll tax were $62.4 million in the GAAP reconciliation. Source

Segment revenue

  • Oncology revenue rose 38%: Oncology revenue was $219.1 million, up from $158.7 million, driven primarily by test volume. Source
  • Screening revenue grew over 250%: Screening revenue was $52.9 million, against $14.8 million, driven primarily by Shield screening test volume. Source
  • Biopharma & Data grew 9%: Biopharma & Data revenue was $60.9 million, up from $56.0 million, an increase of 9%. Source
  • Licensing and other revenue declined: Licensing and other revenue was $2.1 million, compared with $2.6 million in the prior year period. Source

“Growth was fueled by strong oncology volume, with acceleration across every product.”

Helmy Eltoukhy, co-founder and co-CEO

Products, approvals and coverage

  • Liquid CDx panel gained FDA approval: The company reported FDA approval for Guardant360 Liquid CDx, which it described as the most advanced FDA-approved liquid biopsy panel. Source
  • Companion diagnostic approved for lung cancer: FDA approved Guardant360 CDx as a companion diagnostic for Boehringer Ingelheim's HERNEXEOS in HER2-mutant advanced non-small cell lung cancer. Source
  • Shield added to cancer society guidelines: The American Cancer Society's updated colorectal cancer screening guidelines now include Shield, according to the company. Source
  • UnitedHealth Group covers Shield: UnitedHealth Group is described as the first major commercial insurer to provide Shield coverage. Source
  • Higher-throughput Shield workflow approved: FDA approved a higher-throughput, lower-COGS Shield workflow, according to the company. Source
  • 38 abstracts presented at ASCO: The company presented 38 abstracts at the 2026 ASCO Annual Meeting, which it said highlight the expanding clinical utility of its portfolio. Source

Test volumes

  • Oncology tests rose 63%: Oncology test volume was about 104,000 tests, an increase of 63% over the prior year period. Source
  • Shield tests reached about 66,000: Shield screening tests were about 66,000 in the quarter, against about 16,000 in the prior year period. Source
  • Shield tests were 44,000 in Q1: The prior-quarter release reported about 44,000 Shield screening tests in the first quarter of 2026.
  • Oncology tests were 86,000 in Q1: The prior-quarter release reported about 86,000 oncology tests in the first quarter of 2026, up 47% year over year.

“The inclusion of the Shield blood test in the American Cancer Society’s screening guidelines, together with UnitedHealth Group’s broad coverage decision, represents powerful validation of Shield’s clinical utility and its potential to improve access to screening.”

AmirAli Talasaz, co-founder and co-CEO

Costs and margins

  • Non-GAAP gross margin was 67%: Non-GAAP gross margin was 67%, against 66% in the prior year period. Source
  • GAAP gross margin held at 65%: GAAP gross margin was 65% for the second quarter of 2026, the same as the prior year period. Source
  • GAAP operating expenses rose: Operating expenses were $348.1 million against $257.3 million; the company cited stock-based compensation as a further driver. Source
  • Non-GAAP operating expenses reached $288.3M: Non-GAAP operating expenses were $288.3 million against $215.3 million, driven by commercial infrastructure and marketing for Shield and Oncology. Source

Cash flow and capital

  • Free cash flow used $69.5 million: Free cash flow was negative $69.5 million, against negative $65.9 million a year earlier; first-half free cash flow was negative $140.7 million. Source
  • Capital expenditures rose to $11.8M: Purchases of property and equipment were $11.8 million in the quarter, compared with $5.6 million a year earlier. Source
  • Cash position of $1.2 billion: Cash, cash equivalents and restricted cash totaled $1.2 billion at June 30, 2026; the prior release also included marketable securities. Source
  • Shares outstanding increased: Shares outstanding were 133,612,678 at June 30, 2026, up from 130,635,301 at December 31, 2025. Source

Full-year 2026 guidance

  • Revenue guidance raised by $40 million: The company raised full-year revenue guidance by $40 million at both ends of the range, to growth of 36% to 38%. Source
  • Oncology volume growth guidance lifted: Oncology volume growth for 2026 is now expected at about 50%, up from about 35%, with revenue growth at about 30%. Source
  • Screening revenue guidance raised: Screening revenue is now expected at $218 to $230 million, from $186 to $198 million, on Shield volume of 270,000 to 285,000 tests. Source
  • Gross margin guidance held: Full-year non-GAAP gross margin guidance of 64% to 65% was continued, unchanged from the prior release. Source
  • Operating expense guidance raised: Non-GAAP operating expenses are now expected at $1.08 to $1.10 billion, up from $1.05 to $1.07 billion. Source
  • Free cash flow burn guidance raised: Full-year free cash flow burn is now expected at $195 to $205 million, against the previous $185 to $195 million. Source

Coming up, as management said on 30 July 2026

  • Laboratory capacity investment accelerating: The company said the revised free cash flow range reflects accelerated investment in laboratory capacity for Shield volume growth. Source

Figures management reported

FigureReported
Oncology test volume Sourceapproximately 104,000 tests, up 63%
Shield screening tests Sourceapproximately 66,000 tests, against 16,000 in the prior year period

Earlier plans management reported on

  • Not stated: The company continues to expect non-GAAP gross margin of 64% to 65% for full-year 2026, as stated in the prior guidance. Source
  • Not stated: The prior release said the company continued to expect Biopharma & Data growth in the low double-digit range; the current release says it is expected in that range.

Other quarters

Summarised with AI from the documents the company filed with the SEC. Every point is checked against the filing before it is shown: management’s own words word for word, figures against the line or table row they come from. A point that fails the check is left out. Source opens the filing at that line.