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Gilead (GILD) Q2 FY26 earnings call: guidance and Q&A

Earnings call· Jun 2026 (Q2 FY26)· Health Care· Aug 4, 2026

Source: earnings call transcript

Executive summary

Gilead Q2 FY26 — Strong Commercial Execution and Pipeline Advancement

Gilead delivered a strong second quarter, marked by robust commercial execution across its core therapeutic areas, particularly in HIV and oncology. The company raised its full-year HIV growth expectations and advanced its extensive pipeline through strategic acquisitions and positive clinical readouts. Management remains focused on integrating new programs and preparing for several key product launches in the near term, while continuing to diversify its portfolio.

Highlights

5
  • Base business sales increased 10% year-over-year to $7.6 billion, driven by HIV, Trodelvy, and Livdelzi.

  • HIV sales grew 12% year-over-year to $5.7 billion, with Biktarvy sales up 7% to $3.8 billion.

  • PrEP business sales doubled year-over-year, exceeding $1 billion quarterly for the first time, with an annual run rate of $4 billion.

  • Trodelvy sales were up 26% year-over-year to $457 million, driven by strong demand and new first-line approvals.

  • Livdelzi sales more than doubled year-over-year to $167 million, establishing it as the leading second-line PBC regimen.

Concerns

3
  • Cell therapy sales were down 14% year-over-year to $417 million due to ongoing in and out-of-class competition.

  • Veklury sales are now expected to be approximately $300 million for FY26, down from $600 million previously, reflecting lower COVID-19 hospitalizations.

  • HIV treatment market growth slowed in Q2 due to changes in the Affordable Care Act, impacting patient insurance coverage.

Guidance & targets

CategoryTargetConfidence
Full-year HIV sales growth
9% to 10% year-over-year
high materiality
High
Full-year Yeztugo sales
approximately $1 billion
medium materiality
High
Full-year base business sales
$29.8 billion to $30.1 billion
high materiality
High
Full-year total product sales
$30.1 billion to $30.4 billion
high materiality
High
Full-year Veklury sales
approximately $300 million
medium materiality
High
Full-year acquired IPR&D expenses
$11.5 billion
high materiality
High
Full-year R&D expenses
increase mid-single-digit percentage on a dollar basis
medium materiality
High
Full-year SG&A expenses
increase mid-single-digit percentage on a dollar basis
medium materiality
High
Full-year non-GAAP effective tax rate
140% and 115%
medium materiality
High
Full-year non-GAAP effective tax rate (excluding acquisitions)
20%
medium materiality
High
Full-year non-GAAP EPS
negative $0.65 to negative $0.30
high materiality
High
Full-year non-GAAP diluted EPS (illustrative, excluding acquisitions and nonrecurring revenue)
$8.50 to $8.85
high materiality
High
Cell therapy sales decline
mid-teens percentage year-over-year
medium materiality
High

Segment performance

SegmentRevenueYoYQoQMargin
HIV
Strong performance driven by Biktarvy in treatment and Descovy/Yeztugo in PrEP, with higher average realized price and demand. Sequential growth also driven by inventory build and typical seasonality.
Biktarvy sales: $3.8BBiktarvy growth YoY: 7%Biktarvy growth QoQ: 12%PrEP sales: >$1BPrEP growth YoY: >100%Yeztugo sales: $232MYeztugo growth QoQ: 40%Descovy PrEP sales: ~$801MDescovy PrEP growth YoY: 60%
$5.7B12%13%—
Oncology
Exceptional growth for Trodelvy driven by strong demand across triple-negative and pretreated HR-positive/HER2-negative metastatic breast cancer, and new first-line approvals.
Trodelvy sales: $457MTrodelvy growth YoY: 26%Trodelvy growth QoQ: 13%
————
Cell Therapy
Sales decline year-over-year due to expected ongoing in and out-of-class competition. Sequential growth driven by increased Yescarta demand, partially offset by competitive pressures for Tecartus.
$417M-14%2%—
Liver Disease
Overall growth reflects increased demand across PBC, HBV, and HDV, partially offset by lower HCV starts. Livdelzi continues to gain momentum as the leading second-line PBC regimen.
Livdelzi sales: $167MLivdelzi growth YoY: >100%Livdelzi growth QoQ: 26%
$877M10%14%—

Product announcements

ProductTypeDetails
Hepcludexlaunch
Trodelvyexpansion

Deals & partnerships

Tubulis Acquisition of an industry-leading ADC platform and promising clinical stage ADCs.

Provides novel linker and payload technologies, complementing Gilead's ADC leadership. Closed this quarter.

Arcellx Acquisition to gain full ownership of anito-cel and the D-Domain binder platform.

Enables faster, more focused execution in multiple myeloma and future opportunities in CAR T. Closed in April.

Ouro Medicines Acquisition adding bispecific T-cell engager assets.

Expands the breadth of Gilead's innovation engine. Closed this quarter.

Merck Collaboration on once-weekly oral HIV treatment regimen (islatravir + lenacapavir).

Shared positive Phase III data for ISL/LEN at IAS. Working towards global regulatory filings and potential launch in 2027.

Pregene Collaboration to accelerate in vivo CAR T platform development.

Enables speed to clinic for updated in vivo platform, with two investigator-sponsored studies starting later this year.

Risks & headwinds

Competition in cell therapy Q2 FY26 and ongoing

Cell therapy sales down 14% YoY

Mitigation:Launch readiness activities for anito-cel, focus on differentiated profile, expanding D-Domain binder platform for future CAR T opportunities.

Decline in Veklury sales FY26

Full-year Veklury sales guidance reduced from $600M to $300M

Mitigation:Focus on growth in base business and new product launches to offset decline.

Impact of Affordable Care Act (ACA) changes on HIV treatment market Q2 FY26, expected to normalize

Slowing in HIV treatment market growth in Q2

Mitigation:Monitoring patient navigation of insurance changes; expect trend back to typical 2-3% annual growth rate.

What to watch in Q3 FY26

BIC/LEN FDA decision

Q3 FY26
Current Expected later this month (August)
Target Approval decision

Why it matters

This is a key regulatory catalyst for a new daily oral HIV treatment option, crucial for expanding Gilead's leadership in the switch market.

Later this month, we expect an FDA decision on our once-daily oral treatment combining bictegravir and lenacapavir.

Find out whether GILD delivers this. Inve re-checks your case every morning.

Q&A highlights

Can you explain the growing delta between Yeztugo prescription trends (IQVIA) and reported sales, and what are the biggest growth drivers for Yeztugo through year-end?

Gilead will not comment on IQVIA data but is confident in its own reported data. Key growth drivers for Yeztugo include strong uptake in naive and switch markets, growing HCP confidence, the expanding PrEP market (14% YoY growth), and a high persistency rate of over 70% at 6 months. The company remains confident in its $1 billion full-year sales guidance for Yeztugo.

“For Yeztugo, as you think about the back half of this year, really building on a really strong first half. And I would say that we expect strong continued launch momentum because we're still in launch mode. And that's really driven by the strong uptake we've been seeing in both naive and switch market, the growing confidence that we're seeing with our health care professionals with access pathways, logistics, experience with Yeztugo.”

asked by Tyler Van Buren · answered by Johanna Mercier

2 min read 6 chapters

Detailed narrative

HIV Portfolio Strength and Pipeline Expansion

Gilead's HIV business demonstrated significant strength, with overall sales up 12% year-over-year. Biktarvy continued its leadership in treatment, while the PrEP business, driven by Descovy and Yeztugo, doubled year-over-year to exceed $1 billion in quarterly sales. The company is expanding its HIV pipeline with potential new daily, weekly, monthly, twice-yearly, and yearly options, including an anticipated FDA decision for BIC/LEN and planned launch of ISL/LEN in 2027.

Oncology Growth and ADC Platform Advancement

Trodelvy sales grew 26% year-over-year, benefiting from strong demand in metastatic breast cancer and recent FDA approvals for first-line metastatic triple-negative breast cancer. The acquisition of Tubulis closed, providing an industry-leading ADC platform and promising clinical-stage ADCs like GS-8824 (formerly TUB-040) which showed encouraging Phase I data in platinum-resistant ovarian cancer. Gilead aims to be a leader in ADC innovation long-term.

Cell Therapy Progress and Anito-cel Launch Readiness

Despite a 14% year-over-year decline in cell therapy sales due to competition, Gilead is actively preparing for the potential launch of anito-cel for multiple myeloma, with a PDUFA date in December. The acquisition of Arcellx gives full ownership of anito-cel and the D-Domain binder platform, enabling faster execution and future opportunities in CAR T.

Enrollment for iMMagine-3 in second-line multiple myeloma was completed, with potential filing as early as 2027.

Liver Disease Momentum and New Approvals

The liver disease business saw strong performance, with Livdelzi sales more than doubling year-over-year and gaining momentum as the leading second-line treatment for primary biliary cholangitis (PBC). Positive Phase III IDEAL data further strengthens Livdelzi's opportunity. Hepcludex was also launched in the U.S. as the first and only FDA-approved treatment for chronic hepatitis delta virus (HDV), addressing a small but underserved patient population.

Strategic Acquisitions and Pipeline Diversification

Gilead completed acquisitions of Arcellx, Tubulis, and Ouro Medicines, significantly expanding its pipeline in cell therapy, antibody-drug conjugates, and bispecific T-cell engagers. These acquisitions complement the company's existing pipeline and support its long-term strategy to diversify beyond virology into oncology and inflammation. The company does not anticipate additional sizable M&A this year but remains opportunistic.

Financial Performance and Capital Allocation

The company reported strong base business growth and raised its full-year sales and illustrative EPS guidance. Non-GAAP diluted EPS, excluding acquired IPR&D and nonrecurring revenue, grew approximately 13% year-over-year. Gilead returned nearly $1.4 billion to shareholders in Q2, including $355 million in share repurchases, representing approximately 49% of free cash flow returned in the first half of 2026.

Summary of the company's earnings call; see how call summaries are prepared. Not investment advice.