revenue
29800–30100 $million
FY 2026
official guidance
| Revenue | $29.7B |
|---|---|
| Operating income | $10.4B |
| Net income | $9.2B |
| Free cash flow | $10.2B |
| Operating margin | 34.9% |
| Net margin | 31.0% |
| Return on equity | 39.2% |
| Period | TTM 2026-03-31 |
OpenFilings 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 2026Hold: 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.
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.
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.
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.
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.