Companies/US/GILD

GILEAD SCIENCES, INC.

Last · —$153.54+5.62 (+3.80%)live · yahoo · 1s ago
Vol 5.57M ≈ 855.26M
Market cap$197.13B—
P/E · TTM20.4fwd — · eps —
Beta—vs S&P 500
Div yield—annual · TTM
52w range
——
Volume—session

Issuer

Legal nameGILEAD SCIENCES, INC.
HQUnited States (US)
ListingUS GILD
ISINUS3755581036
SectorHealthcare
IndustryDrugs (Biotechnology)
SIC2836
CurrencyUSD
Entity registrysec:0000882095
CIK0000882095
LinkedIn
Employees17,000
AddressGilead Sciences, Inc. 333 Lakeside Drive 94404, Foster City +650 574 3000
Headline financial metrics
Revenue$29.7B
Operating income$10.4B
Net income$9.2B
Free cash flow$10.2B
Operating margin34.9%
Net margin31.0%
Return on equity39.2%
PeriodTTM 2026-03-31
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OpenFilings analyst

Our analyst

Agentic read of the latest earnings call — recommendation updates when we process a new transcript. Research synthesis, not investment advice.

Strong operating momentum is not yet enough to offset acquisition charges and competitive Cell Therapy pressure.

Latest call · Q2 2026

Hold: Gilead’s underlying business is accelerating, with Q2 base sales up 10% to $7.6 billion, HIV sales up 12% to $5.7 billion, and full-year base-sales guidance raised to $29.8-$30.1 billion.

However, the investment case is offset by mid-teens expected Cell Therapy declines, $11.5 billion of acquired IPR&D, and full-year non-GAAP EPS guidance of negative $0.65 to negative $0.30; the core business is strong, but acquisition integration and pipeline execution still need to prove shareholder value.

Themes
  • Hiv Growth
  • Prep
  • Yeztugo
  • Biktarvy
  • Trodelvy
  • Cell Therapy Competition
+2

Near term

FDA decision on BIC/LEN is expected by August 27, providing a near-term HIV treatment catalyst.

Anito-cel’s December 23 PDUFA date could materially affect the Cell Therapy outlook, but launch execution and competitive uptake remain unproven.

Yeztugo is targeting approximately $1 billion of 2026 sales after Q2 sales of $232 million, while quarterly PrEP sales exceeded $1 billion for the first time.

Trodelvy’s first-line metastatic TNBC launch and the upcoming ASCENT-GYN Phase 3 update are important tests of oncology growth.

Longer term

HIV remains the clearest structural growth engine: PrEP is running at a $4 billion annualized rate, while weekly, twice-yearly, and yearly options could extend Gilead’s leadership.

Livdelzi’s PBC expansion and Hepcludex’s HDV launch add growth, but Hepcludex is expected to be only a modest contributor and HCV remains a drag.

Arcellx, Tubulis, and Ouro acquisitions broaden the cell therapy, ADC, and bispecific pipeline, but value creation depends on successful integration and clinical validation.

Cell Therapy competition is a material moat risk: Q2 sales fell 14% year over year and management now expects a mid-teens full-year decline.

Trodelvy and the Tubulis ADC platform could diversify oncology growth, but GS-8824 remains early-stage despite encouraging Phase 1 data.

Red flags

Management’s headline non-GAAP EPS is negative because of $11.5 billion of acquired IPR&D and related tax effects; the $8.50-$8.85 illustrative EPS figure excludes approximately $9.15 per share of acquisition-related costs and financing expenses.

Cell Therapy is still contracting despite anito-cel launch preparation, indicating that near-term competitive pressure is not resolved.

The acquisitions materially increase execution and integration risk, while management does not expect another sizeable M&A transaction this year.

Biktarvy demand faced lower-than-expected effects from Affordable Care Act changes, and HIV treatment market growth temporarily slowed in Q2.

No analyst Q&A was provided, so there is limited evidence on valuation, acquisition returns, pricing sustainability, or competitive responses.

Forward outlook

revenue

29800–30100 $million

FY 2026

official guidance

revenue growth

6–7 pct

FY 2026

official guidance

revenue growth

9–10 pct

FY 2026

official guidance

revenue

1000 $million

FY 2026

official guidance

revenue

30100–30400 $million

FY 2026

official guidance

revenue

300 $million

FY 2026

official guidance

eps diluted

-0.65–-0.3 $per share

FY 2026

official guidance

adjusted eps

8.5–8.85 $per share

FY 2026

management framework

OpenFilings analyst view from primary-source filings and earnings calls — not investment advice.

From latest 10-K · 2026-02-24

  • Hiv Growth
  • Yeztugo Launch
  • Biktarvy Exclusivity
  • Oncology Pipeline
  • Clinical Hold
  • Car T Manufacturing
  • Customer Concentration

Red flags

  • Approximately 60% of accounts receivable relates to three wholesalers and their specialty distributor affiliates, creating meaningful counterparty and channel concentration.
  • The HIV treatment trials for GS-1720 and/or GS-4182 were placed on clinical hold; these candidates are not approved anywhere globally.
  • Trodelvy’s Phase 3 ASCENT-07 study failed its primary progression-free-survival endpoint in first-line HR+/HER2- metastatic breast cancer, limiting a major oncology expansion opportunity.
  • Gilead plans a $32 billion U.S. investment through 2030, increasing execution and capital-allocation exposure even as 2025 revenue growth was only 2%.

Upcoming earnings

1 event
9:00 PM UTC+1
Period
Sep 2026
Est. EPS
$2.19
Est. revenue
7.8B

Earnings transcripts

12 of 23 recent

Documents

FormReporting forFiledFlags
2026-10-012026-10-020
2026-09-222026-09-230
2026-09-152026-09-160
2026-09-152026-09-160
2026-09-102026-09-110