
($ in millions, except percentages) | Q326 | Yr/Yr | Qtr/Qtr | Management Commentary |
HIV (Includes HIV Treatment and Prevention) | $6,249 | 18% | 10% |
~9-10% after Q226; was ~6% at start 2026). |
Biktarvy | $4,059 | 10% | 8% |
|
HIV Prevention (PrEP) *Estimated based on 80% of Descovy sales plus Yeztugo sales | $1,142* | ~2X | 11%* |
|
($ in millions, except percentages) | Q326 | Yr/Yr | Qtr/Qtr | Management Commentary |
Descovy (~80% of Descovy's business is PrEP) | $1,046 | 49% | 8% |
|
Yeztugo (Launched June 2025) | $305 | NM | 31% |
|
Liver Disease | $927 | 13% | 6% |
|
Livdelzi (Launched August 2024) | $203 | 93% | 21% |
|
Oncology | $860 | 9% | (2)% | |
Cell Therapy (Includes Yescarta and Tecartus) | $355 | (18)% | (15)% |
|
($ in millions, except percentages) | Q326 | Yr/Yr | Qtr/Qtr | Management Commentary |
Trodelvy | $506 | 42% | 11% |
|
Other (Includes AmBisome, Cayston, Jyseleca, Letairis, Zydelig) | $167 | (9)% | 4% | |
Product sales excluding Veklury | $8,203 | 16% | 8% |
|
Veklury | $86 | (69)% | NM | - YoY and QoQ reflects fewer COVID-19 related hospitalizations. |
Product sales | $8,289 | 13% | 9% | |
Royalty, contract and other | $11 | (97)% | (94)% | - YoY and QoQ reflecting revenues recognized in prior periods related to a previous sale of intellectual property, which did not repeat. |
Total revenues | $8,300 | 7% | 6% |
NM - Not Meaningful
Q326 Key Portfolio HighlightsManagement Commentary | |
Virology | |
HIV Treatment Pipeline |
+ GS-3242, an INSTI-based long-acting injectable treatment regimen; expect to initiate Q6M dosing cohorts following additional Phase 1 data in higher dose. |
PrEP Pipeline |
|
Management Commentary | |
Oncology | |
Trodelvy & Solid Tumor Pipeline |
|
Cell Therapy |
|
Inflammation | |
Emvistegrast |
|
Gamgertamig | - Continue expect to share Phase 1 data for gamgertamig (BCMAxCD3) in immune thrombocytopenia at a medical congress later this year. |
Edecesertib | - Expect to share detailed update from Phase 2a COSMIC study of edecesertib (IRAK4) in cutaneous lupus erythematosus at the ACR meeting on Nov. 8, 2026. |
Livdelzi | - Expect to share detailed results from Phase 3 IDEAL study of Livdelzi in PBC patients with ALP levels 1.0 - 1.67x ULN or intolerant to UDCA at AASLD 2026. |
Program | Trial | Indication | Update | Status |
Virology | ||||
ISL/LEN | ISLEND-1 & 2 | QW Oral HIV Tx | Phase 3 Update | Completed & data shared |
Hepcludex | MYR301 | HDV | FDA Decision | Completed & launched |
Bixlenvo | ARTISTRY-1 & 2 | QD Oral HIV Tx | FDA Decision | Completed & launched |
Oncology | ||||
Trodelvy | ASCENT-03 & -04 | 1L mTNBC (PD-L1-) 1L mTNBC (PD-L1+) | FDA Decision | Completed & launched |
ASCENT-GYN | A/R Endometrial Cancer | Phase 3 Update | Expected 2H26 | |
EVOKE-03 | 1L mNSCLC (PD-L1 High) | Phase 3 Update | Completed; did not meet endpoint | |
Anito-cel | iMMagine-1 | 4L+ R/R MM | FDA Decision | Expected December 23, 2026 |
Inflammation | ||||
Livdelzi | IDEAL | 2L PBC | Phase 3 Update | Completed |
(in millions, except percentages) | Q326 | Yr/Yr | Qtr/Qtr |
Net cash provided by operating activities | $5,035 | 23% | 41% |
Less: Purchases of property, plant and equipment | $(237) | 61% | 69% |
Free cash flow | $4,798 | 21% | 40% |
Cash, cash equivalents and marketable debt securities | $6,437 | (31)% | NM |
Debt repaid | $19 | NM | 17% |
Cash dividends paid | $1,039 | 3% | 1% |
Share repurchases | $370 | (15)% | 4% |
(in millions, except percentages) | Q326 | Yr/Yr | Qtr/Qtr |
Total product sales - U.S. | $6,361 | 21% | 14% |
Total product sales - Europe | $1,058 | (7)% | (8)% |
Total product sales - Rest of World | $869 | (6)% | -% |
Total product sales | $8,289 | 13% | 9% |
(in millions, except percentages and per share amounts) | Q326 | Yr/Yr | Qtr/Qtr | Management Commentary |
Cost of goods sold | $983 | (1)% | (2)% | |
Product gross margin | 88% | 165 bps | 124 bps | - YoY driven by expiration of a TAF-related royalty obligation in November 2025. |
Research and development expenses | $1,591 | 19% | 11% | - YoY and QoQ reflects higher compensation-accruals related to our financial outperformance YTD and higher clinical costs. |
Acquired IPR&D expenses | $18 | (89)% | (100)% | |
Selling, general and administrative expenses | $1,539 | 14% | 1% | - YoY primarily reflects HIV promotional activities, legal expenses and higher compensation-accruals related to financial outperformance YTD. |
Total operating expenses | $3,148 | 10% | (78)% | |
Operating income | $4,168 | 6% | NM | |
Operating margin | 50.2% | -25 bps | NM |
|
Effective tax rate | 19.0% | 149 bps | NM | - In-line with FY26 expectation of ~20%, excluding acquired IPR&D expenses related to our 2026 acquisitions. |
Net income | $3,186 | 3% | NM | |
Diluted earnings per share | $2.55 | 3% | NM |
|
Shares used in diluted earnings per share calculation | 1,251 | -% | 1% |
NM - Not Meaningful
(in millions, except percentages and per share amounts) | FY26 | Management Commentary |
Total product sales | $31.0 billion - $31.3 billion | - Was $30.1 billion - $30.4 billion. |
Veklury | ~ $300 million | - Unchanged |
Total product sales excluding Veklury | $30.7 billion - $31.0 billion |
|
HIV | ~12% |
|
Non-GAAP | ||
Product gross margin | ~ 87.0% | - Unchanged |
R&D | Mid to high single-digit % growth on a dollar basis |
|
Acquired IPR&D | ~ $12.9 billion |
|
SG&A | High-single digit % growth on a dollar basis |
|
Operating income | $2.0 billion - $2.4 billion | - Was $2.9 billion- $3.3 billion. |
Certain amounts and percentages in this document may not sum or recalculate due to rounding.
(in millions, except percentages and per share amounts) | FY26 | Management Commentary |
Effective tax rate | ~ 220% - 165% | - Was ~ 140% - 115%.
~20% (no change from February guidance). |
Diluted EPS | $(1.20) - $(0.85) | - Was $(0.65) - $(0.30). - Excluding ~$9.95 per share relating to the acquired IPR&D expense and full-year financing costs associated with the acquisitions this year and non-recurring other revenue, FY26 non-GAAP diluted EPS would be $8.75 - $9.10 (raised $0.25 on both ends from illustrative August guidance due to higher base sales, partially offset by higher OpEx). |
GAAP Diluted EPS | $(4.40) - $(4.05) | - Was $(3.75) - $(3.40). |
Certain amounts and percentages in this document may not sum or recalculate due to rounding.
Maximum Fair Price Management Commentary |
|
Three Months Ended Nine Months Ended September 30, September 30,
(in millions, except per share amounts) 2026 2025 2026 2025
Revenues:Product sales | $ 8,289 $ 7,345 $ 22,862 $ 21,013 | |||
Royalty, contract and other revenues | 11 424 201 505 | |||
Total revenues | 8,300 7,769 23,063 21,518 | |||
Costs and expenses: | ||||
Cost of goods sold | 1,571 1,569 4,595 4,610 | |||
Research and development expenses | 1,608 1,346 4,744 4,215 | |||
Acquired in-process research and development expenses | 18 170 11,307 485 | |||
In-process research and development impairments | - - 1,750 190 | |||
Selling, general and administrative expenses | 1,641 1,357 5,013 3,980 | |||
Total costs and expenses | 4,838 4,442 27,409 13,480 | |||
Operating income (loss) | 3,462 3,327 (4,346) 8,038 | |||
Interest expense | 269 256 756 769 | |||
Other (income) expense, net | 130 (569) (492) (449) | |||
Income (loss) before income taxes | 3,063 3,641 (4,610) 7,718 | |||
Income tax expense | 634 589 1,435 1,391 | |||
Net income (loss) | $ 2,429 $ 3,052 $ (6,045) $ 6,327 | |||
Basic earnings (loss) per share | $ 1.96 $ 2.46 $ (4.87) $ 5.08 | |||
Diluted earnings (loss) per share | $ 1.94 $ 2.43 $ (4.87) $ 5.04 | |||
Shares used in basic earnings (loss) per share calculation | 1,242 1,243 1,242 1,245 | |||
Shares used in diluted earnings (loss) per share calculation | 1,251 1,254 1,242 1,256 | |||
Supplemental Information: | ||||
Cash dividends declared per share | $ 0.82 | $ 0.79 | $ 2.46 | $ 2.37 |
Product gross margin | 81.0 % | 78.6 % | 79.9 % | 78.1 % |
Research and development expenses as a % of revenues | 19.4 % | 17.3 % | 20.6 % | 19.6 % |
Selling, general and administrative expenses as a % of revenues | 19.8 % | 17.5 % | 21.7 % | 18.5 % |
Operating margin | 41.7 % | 42.8 % | (18.8)% | 37.4 % |
Effective tax rate | 20.7 % | 16.2 % | (31.1)% | 18.0 % |
Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||
(in millions, except percentages) | 2026 | 2025 | Change | 2026 | 2025 | Change | ||||
Product sales: | ||||||||||
HIV | $ 6,249 | $ 5,277 | 18% | $ 16,972 | $ 14,952 | 14% | ||||
Liver Disease | 927 | 819 | 13% | 2,571 | 2,372 | 8% | ||||
Oncology | 860 | 788 | 9% | 2,543 | 2,395 | 6% | ||||
Other | 167 | 184 | (9)% | 524 | 594 | (12)% | ||||
Total product sales excluding Veklury | 8,203 | 7,068 | 16% | 22,610 | 20,313 | 11% | ||||
Veklury | 86 | 277 | (69)% | 253 | 700 | (64)% | ||||
Total product sales | 8,289 | 7,345 | 13% | 22,862 | 21,013 | 9% | ||||
Royalty, contract and other revenues | 11 | 424 | (97)% | 201 | 505 | (60)% | ||||
Total revenues | $ 8,300 $ 7,769 | 7% | $ 23,063 $ 21,518 | 7% | ||||||
Three Months Ended Nine Months Ended September 30, September 30,
(in millions, except percentages) | 2026 | 2025 | Change | 2026 | 2025 | Change | |
Non-GAAP: | |||||||
Cost of goods sold | $ 983 | $ 992 | (1)% | $ 2,851 | $ 2,875 | (1)% | |
Research and development expenses | $ 1,591 | $ 1,334 | 19% | $ 4,375 | $ 4,123 | 6% | |
Acquired in-process research and development expenses | $ 18 | $ 170 | (89)% | $ 11,307 | $ 485 | NM | |
Selling, general and administrative expenses | $ 1,539 | $ 1,351 | 14% | $ 4,423 | $ 3,931 | 13% | |
Other (income) expense, net | $ (34) | $ (87) | (61)% | $ (171) | $ (251) | (32)% | |
Diluted earnings (loss) per share | $ 2.55 | $ 2.47 | 3% | $ (2.14) | $ 6.29 | NM | |
Shares used in non-GAAP diluted earnings | |||||||
(loss) per share calculation | 1,251 | 1,254 | -% | 1,242 | 1,256 | (1)% | |
Product gross margin | 88.1 % | 86.5 % | 165 bps | 87.5 % | 86.3 % | 121 bps | |
Research and development expenses as a % of revenues | 19.2 % | 17.2 % | 200 bps | 19.0 % | 19.2 % | (19) bps | |
Selling, general and administrative expenses as a % of revenues | 18.5 % | 17.4 % | 115 bps | 19.2 % | 18.3 % | 91 bps | |
Operating margin | 50.2 % | 50.5 % | (25) bps | 0.5 % | 47.0 % | NM | |
Effective tax rate | 19.0 % | 17.5 % | 149 bps | (455.0)% | 17.6 % | NM |
NM - Not Meaningful
(1) Refer to Non-GAAP Financial Information section above for further disclosures on non-GAAP financial measures. A reconciliation between GAAP and non-GAAP financial information is provided in the tables below.
Three Months Ended Nine Months Ended
September 30, September 30, | ||||
(in millions, except percentages and per share amounts) | 2026 | 2025 | 2026 | 2025 |
Cost of goods sold reconciliation: | ||||
GAAP cost of goods sold | $ 1,571 | $ 1,569 | $ 4,595 | $ 4,610 |
Acquisition-related - amortization(1) | (587) | (577) | (1,742) | (1,735) |
Restructuring | (1) | - | (1) | - |
Non-GAAP cost of goods sold $ 983 $ 992 $ 2,851 $ 2,875 | ||||
Product gross margin reconciliation: | ||||
GAAP product gross margin | 81.0 % | 78.6 % | 79.9 % | 78.1 % |
Acquisition-related - amortization(1) | 7.1 % | 7.9 % | 7.6 % | 8.3 % |
Restructuring | - % | - % | - % | - % |
Non-GAAP product gross margin | 88.1 % | 86.5 % | 87.5 % | 86.3 % |
Research and development expenses reconciliation: | ||||
GAAP research and development expenses | $ 1,608 | $ 1,346 | $ 4,744 | $ 4,215 |
Acquisition-related - other costs(2) | (8) | (4) | (344) | (41) |
Restructuring | (8) | (8) | (25) | (52) |
Non-GAAP research and development expenses $ 1,591 $ 1,334 $ 4,375 $ 4,123
IPR&D impairment reconciliation:
GAAP IPR&D impairment | $ - $ - $ 1,750 | $ 190 | ||
IPR&D impairment | - - (1,750) | (190) | ||
Non-GAAP IPR&D impairment | $ - | $ - | $ - | $ - |
Selling, general and administrative expenses reconciliation: | ||||
GAAP selling, general and administrative expenses | $ 1,641 | $ 1,357 | $ 5,013 | $ 3,980 |
Acquisition-related - other costs(2) | (69) | - | (454) | - |
Restructuring | (33) | (5) | (73) | (49) |
Other(3) | - | - | (63) | - |
Non-GAAP selling, general and administrative expenses | $ 1,539 | $ 1,351 | $ 4,423 | $ 3,931 |
Operating income (loss) reconciliation: | ||||
GAAP operating income (loss) | $ 3,462 | $ 3,327 | $ (4,346) | $ 8,038 |
Acquisition-related - amortization(1) | 587 | 577 | 1,742 | 1,735 |
Acquisition-related - other costs(2) | 77 | 4 | 798 | 41 |
Restructuring | 42 | 14 | 99 | 101 |
IPR&D impairment | - | - | 1,750 | 190 |
Other(3) | - | - | 63 | - |
Non-GAAP operating income | $ 4,168 | $ 3,921 | $ 107 | $ 10,104 |
Operating margin reconciliation: | ||||
GAAP operating margin | 41.7 % | 42.8 % | (18.8)% | 37.4 % |
Acquisition-related - amortization(1) | 7.1 % | 7.4 % | 7.6 % | 8.1 % |
Acquisition-related - other costs(2) | 0.9 % | - % | 3.5 % | 0.2 % |
Restructuring | 0.5 % | 0.2 % | 0.4 % | 0.5 % |
IPR&D impairment | - % | - % | 7.6 % | 0.9 % |
Other(3) | - % | - % | 0.3 % | - % |
Non-GAAP operating margin | 50.2 % | 50.5 % | 0.5 % 47.0 % | |
Other (income) expense, net reconciliation: | ||||
GAAP other (income) expense, net | $ 130 | $ (569) | $ (492) $ (449) | |
(Loss) gain from equity securities, net | (164) | 483 | 321 | 198 |
Non-GAAP other (income) expense, net | $ (34) | $ (87) | $ (171) | $ (251) |
Three Months Ended Nine Months Ended
September 30, September 30, | ||||
(in millions, except percentages and per share amounts) | 2026 | 2025 | 2026 | 2025 |
Income (loss) before income taxes reconciliation: | ||||
GAAP income (loss) before income taxes | $ 3,063 | $ 3,641 | $ (4,610) | $ 7,718 |
Acquisition-related - amortization(1) | 587 | 577 | 1,742 | 1,735 |
Acquisition-related - other costs(2) | 77 | 4 | 798 | 41 |
Restructuring | 42 | 14 | 99 | 101 |
IPR&D impairment | - | - | 1,750 | 190 |
Loss (gain) from equity securities, net | 164 | (483) | (321) | (198) |
Other(3) | - | - | 63 | - |
Non-GAAP income (loss) before income taxes $ 3,933 $ 3,752 $ (479) $ 9,586 | ||||
Income tax expense reconciliation: | ||||
GAAP income tax expense | $ 634 | $ 589 | $ 1,435 | $ 1,391 |
Income tax effect of non-GAAP adjustments: | ||||
Acquisition-related - amortization(1) | 121 | 120 | 357 | 360 |
Acquisition-related - other costs(2) | 16 | - | 95 | - |
Restructuring | 9 | 3 | 18 | 18 |
IPR&D impairment | - | - | 415 | 51 |
Loss (gain) from equity securities, net | 30 | (43) | (78) | (33) |
Discrete and related tax charges(4) | (62) | (11) | (64) | (101) |
Non-GAAP income tax expense | $ 747 | $ 657 | $ 2,177 | $ 1,686 |
Effective tax rate reconciliation: | ||||
GAAP effective tax rate 20.7 % | 16.2 % | (31.1)% | 18.0 % | |
Income tax effect of above non-GAAP adjustments and discrete and related tax adjustments(4) (1.7)% | 1.3 % | (423.8)% | (0.4)% | |
Non-GAAP effective tax rate 19.0 % | 17.5 % | (455.0)% | 17.6 % | |
Net income (loss) reconciliation: | ||||
GAAP net income (loss) | $ 2,429 | $ 3,052 | $ (6,045) | $ 6,327 |
Acquisition-related - amortization(1) | 467 | 457 | 1,385 | 1,374 |
Acquisition-related - other costs(2) | 61 | 4 | 703 | 41 |
Restructuring | 33 | 11 | 81 | 83 |
IPR&D impairment | - | - | 1,335 | 139 |
Loss (gain) from equity securities, net | 134 | (440) | (243) | (165) |
Discrete and related tax charges(4) | 62 | 11 | 64 | 101 |
Other(3) | - | - | 63 | - |
Non-GAAP net income (loss) | $ 3,186 | $ 3,095 | $ (2,656) | $ 7,901 |
Diluted earnings (loss) per share reconciliation: | ||||
GAAP diluted earnings (loss) per share | $ 1.94 | $ 2.43 | $ (4.87) | $ 5.04 |
Acquisition-related - amortization(1) | 0.37 | 0.36 | 1.11 | 1.09 |
Acquisition-related - other costs(2) | 0.05 | - | 0.57 | 0.03 |
Restructuring | 0.03 | 0.01 | 0.07 | 0.07 |
IPR&D impairment | - | - | 1.07 | 0.11 |
Loss (gain) from equity securities, net | 0.11 | (0.35) | (0.20) | (0.13) |
Discrete and related tax charges(4) | 0.05 | 0.01 | 0.05 | 0.08 |
Other(3) | - | - | 0.05 | - |
Non-GAAP diluted earnings (loss) per share | $ 2.55 | $ 2.47 | $ (2.14) | $ 6.29 |
Three Months Ended Nine Months Ended
September 30, September 30,
(in millions, except percentages and per share amounts) | 2026 | 2025 | 2026 | 2025 |
Non-GAAP adjustment summary: | ||||
Cost of goods sold adjustments | $ 588 | $ 577 | $ 1,744 | $ 1,735 |
Research and development expenses adjustments | 16 | 12 | 369 | 93 |
IPR&D impairment adjustments | - | - | 1,750 | 190 |
Selling, general and administrative expenses adjustments | 102 | 5 | 590 | 49 |
Total non-GAAP adjustments to costs and expenses | 706 | 594 | 4,453 | 2,067 |
Other (income) expense, net, adjustments | 164 | (483) | (321) | (198) |
Total non-GAAP adjustments before income taxes | 870 | 112 | 4,132 | 1,868 |
Income tax effect of non-GAAP adjustments above | (175) | (79) | (807) | (396) |
Discrete and related tax charges(4) | 62 | 11 | 64 | 101 |
Total non-GAAP adjustments to net income $ 757 $ 43 $ 3,389 $ 1,573
(1) Relates to amortization of acquired intangibles.
(2) Adjustments include integration expenses and contingent consideration fair value adjustments associated with Gilead's recent acquisitions.
(3) Adjustments include donations of equity securities to the Gilead Foundation, a California nonprofit organization, during the first quarter of 2026.
(4) Represents discrete and related deferred tax charges or benefits primarily associated with acquisition-related adjustments and transfers of intangible assets from a foreign subsidiary to Ireland and the United States.
RECONCILIATION OF GAAP TO NON-GAAP 2026 FULL-YEAR GUIDANCE(1) (unaudited)(in millions, except percentages and per share | Provided | Updated | Updated | Updated |
amounts) | February 10, 2026 | May 7, 2026 | August 4, 2026 | October 29, 2026 |
Projected product gross margin GAAP to non-GAAP reconciliation: | ||||
GAAP projected product gross margin | ~ 79.0% | ~ 79.0% | ~ 79.0% | ~ 79.0% |
Acquisition-related expenses | ~ 8.0% | ~ 8.0% | ~ 8.0% | ~ 8.0% |
Non-GAAP projected product gross | ||||
margin | ~ 87.0% | ~ 87.0% | ~ 87.0% | ~ 87.0% |
Projected operating income (loss) GAAP to non-GAAP reconciliation: | ||||
GAAP projected operating income (loss) | $11,400 - $11,900 | $(1,000) - $(500) | $(2,250) - $(1,850) | $(3,150) - $(2,750) |
Acquisition-related, IPR&D impairment, | ||||
restructuring and other expenses | ~ 2,400 | ~ 3,400 | ~ 5,150 | ~ 5,150 |
Non-GAAP projected operating income | $13,800 - $14,300 | $2,400 - $2,900 | $2,900 - $3,300 | $2,000 - $2,400 |
Projected effective tax rate GAAP to non-GAAP reconciliation:(2) | ||||
GAAP projected effective tax rate | ~ 21% | ~ (150%) - (220%) | ~ (80%) - (90%) | ~ (50%) - (55%) |
Income tax effect of above non-GAAP | ||||
adjustments and fair value | ||||
adjustments of equity securities, and | ||||
discrete and related tax adjustments | (~ 1%) | NM | NM | NM |
Non-GAAP projected effective tax rate | ~ 20% | ~ 190% - 140% | ~ 140% - 115% | ~ 220% - 165% |
Projected diluted earnings (loss) per share GAAP to non-GAAP reconciliation: | ||||
GAAP projected diluted earnings (loss) | ||||
per share | $6.75 - $7.15 | $(3.25) - $(2.85) | $(3.75) - $(3.40) | $(4.40) - $(4.05) |
Acquisition-related, IPR&D impairment, | ||||
restructuring and other expenses, fair | ||||
value adjustments of equity securities | ||||
and discrete and related tax | ||||
adjustments ~ 1.70 | ~ 2.20 | ~ 3.10 | ~ 3.20 | |
Non-GAAP projected diluted earnings (loss) per share $8.45 - $8.85 | $(1.05) - $(0.65) | $(0.65) - $(0.30) | $(1.20) - $(0.85) | |
NM - Not Meaningful
(1) Our full-year guidance excludes the potential impact of any (i) acquisitions or business development transactions that have not been executed, (ii) future fair value adjustments of equity securities and (iii) discrete tax charges or benefits associated with changes in tax related laws and guidelines that have not been enacted, as Gilead is unable to project such amounts. The non-GAAP full-year guidance includes non-GAAP adjustments to actual current period results as well as adjustments for the known future impact associated with events that have already occurred, such as future amortization of our intangible assets and the future impact of discrete and related deferred tax charges or benefits primarily associated with transfers of intangible assets from a foreign subsidiary to Ireland and the United States.
(2) The GAAP and non-GAAP projected effective tax rates for the October 29, 2026 update include the impact of Acquired IPR&D expenses related to the acquisitions of Arcellx, Tubulis and Ouro Medicines, which are not deductible for tax purposes. Without these Acquired IPR&D expenses, the GAAP and non-GAAP projected effective tax rate for FY26 would be ~21% and ~20%, respectively.
CONDENSED CONSOLIDATED BALANCE SHEETS (unaudited)September 30, December 31,
(in millions) 2026 2025
AssetsCash, cash equivalents and marketable debt securities | $ 6,437 | $ 10,605 |
Accounts receivable, net | 5,007 | 4,913 |
Inventories(1) | 4,424 | 4,368 |
Property, plant and equipment, net | 5,945 | 5,606 |
Intangible assets, net | 13,424 | 16,978 |
Goodwill | 8,314 | 8,314 |
Other assets | 7,858 | 8,239 |
Total assets Liabilities and Stockholders' Equity | $ 51,408 | $ 59,023 |
Current liabilities | $ 12,002 | $ 11,813 |
Long-term liabilities | 26,451 | 24,592 |
Stockholders' equity(2) | 12,955 | 22,618 |
Total liabilities and stockholders' equity | $ 51,408 | $ 59,023 |
(1) Includes current and long-term inventories, which are disclosed separately in the notes to our financial statements in Form 10-K and Form 10-Q.
(2) As of September 30, 2026 and December 31, 2025, there were 1,241 of shares of common stock issued and outstanding.
SELECTED CASH FLOW INFORMATION (unaudited)Three Months Ended Nine Months Ended September 30, September 30,
(in millions) | 2026 | 2025 | 2026 | 2025 |
Net cash provided by operating activities | $ 5,035 $ 4,109 $ 11,152 $ 6,692 | |||
Net cash used in investing activities | (244) (427) (8,821) (2,958) | |||
Net cash used in financing activities | (1,528) (1,490) (3,423) (6,482) | |||
Effect of exchange rate changes on cash and cash equivalents | (4) (5) (34) 87 | |||
Net change in cash and cash equivalents | 3,259 2,187 (1,126) (2,661) | |||
Cash and cash equivalents at beginning of period | 3,179 5,144 7,564 9,991 | |||
Cash and cash equivalents at end of period | $ 6,437 $ 7,330 $ 6,437 $ 7,330 | |||
Three Months Ended Nine Months Ended September 30, September 30, | ||||
(in millions) | 2026 2025 2026 2025 | |||
Net cash provided by operating activities | $ 5,035 $ 4,109 $ 11,152 $ 6,692 | |||
Purchases of property, plant and equipment | (237) (147) (494) (358) | |||
Free cash flow(1) | $ 4,798 $ 3,962 $ 10,657 $ 6,335 | |||
(1) Free cash flow is a non-GAAP liquidity measure. Please refer to our disclosures in the Non-GAAP Financial Information section above.
Biktarvy | U.S. | $ 3,284 | $ 2,940 | $ 8,837 | $ 8,212 | ||||
Europe | 442 | 427 | 1,347 | 1,231 | |||||
Rest of World | 333 | 320 | 1,009 | 922 | |||||
4,059 | 3,686 | 11,193 | 10,366 | ||||||
Descovy | U.S. | 998 | 652 | 2,680 | 1,791 | ||||
Europe | 22 | 23 | 69 | 67 | |||||
Rest of World | 26 | 25 | 71 | 81 | |||||
1,046 | 701 | 2,820 | 1,939 | ||||||
Genvoya | U.S. | 301 | 323 | 752 | 950 | ||||
Europe | 27 | 34 | 97 | 114 | |||||
Rest of World | 12 | 19 | 44 | 54 | |||||
339 | 377 | 892 | 1,118 | ||||||
Odefsey | U.S. | 226 | 206 | 550 | 642 | ||||
Europe | 52 | 61 | 170 | 184 | |||||
Rest of World | 8 | 10 | 27 | 30 | |||||
286 | 277 | 747 | 857 | ||||||
Symtuza - Revenue share(1) | U.S. | 103 | 95 | 315 | 265 | ||||
Europe | 26 | 26 | 85 | 88 | |||||
Rest of World | 3 | 3 | 8 | 9 | |||||
132 | 124 | 407 | 362 | ||||||
Yeztugo | U.S. | 294 | 39 | 676 | 54 | ||||
Europe | - | - | - | - | |||||
Rest of World | 10 | - | 26 | - | |||||
305 | 39 | 702 | 54 | ||||||
Other HIV(2) | U.S. | 55 | 43 | 114 | 144 | ||||
Europe | 22 | 22 | 72 | 85 | |||||
Rest of World | 5 | 8 | 24 | 28 | |||||
82 | 73 | 211 | 256 | ||||||
Total HIV | U.S. | 5,261 | 4,299 | 13,924 | 12,059 | ||||
Europe | 591 | 592 | 1,839 | 1,769 | |||||
Rest of World | 397 | 386 | 1,209 | 1,124 | |||||
6,249 | 5,277 | 16,972 | 14,952 | ||||||
Livdelzi | U.S. | 176 | 93 | 437 | 207 |
Europe | 26 | 11 | 65 | 16 | |
Rest of World | 1 | - | 1 | - | |
203 | 105 | 503 | 223 | ||
Sofosbuvir / Velpatasvir(3) | U.S. | 139 | 146 | 422 | 497 |
Europe | 59 | 65 | 200 | 227 | |
Rest of World | 76 | 97 | 237 | 273 | |
274 | 309 | 860 | 996 | ||
Vemlidy | U.S. | 170 | 136 | 385 | 358 |
Europe | 13 | 12 | 40 | 36 | |
Rest of World | 151 | 132 | 435 | 389 | |
333 | 280 | 860 | 783 | ||
Other Liver Disease(4) | U.S. | 39 | 39 | 74 | 100 |
Europe | 62 | 70 | 219 | 218 | |
Rest of World | 16 | 17 | 56 | 52 | |
117 | 126 | 349 | 370 | ||
Total Liver Disease | U.S. | 524 | 414 | 1,319 | 1,162 |
Europe | 161 | 158 | 523 | 496 | |
Rest of World | 243 | 247 | 729 | 714 | |
927 | 819 | 2,571 | 2,372 | ||
Veklury | |||||
Veklury | U.S. | 63 | 140 | 188 | 390 |
Europe | 12 | 43 | 28 | 84 | |
Rest of World | 11 | 93 | 36 | 225 | |
86 | 277 | 253 | 700 | ||
Oncology Cell Therapy | |||||
Tecartus | U.S. | 24 | 40 | 83 | 122 |
Europe | 31 | 35 | 102 | 107 | |
Rest of World | 5 | 8 | 21 | 25 | |
60 | 83 | 206 | 254 | ||
Yescarta | U.S. | 114 | 123 | 366 | 444 |
Europe | 107 | 151 | 392 | 455 | |
Rest of World | 73 | 75 | 215 | 228 | |
294 | 349 | 973 | 1,127 | ||
Total Cell Therapy | U.S. | 139 | 163 | 450 | 566 |
Europe | 138 | 186 | 494 | 562 | |
Rest of World | 78 | 83 | 235 | 253 | |
355 | 432 | 1,179 | 1,381 | ||
Trodelvy | |||||
Trodelvy | U.S. | 336 | 221 | 896 | 626 |
Europe | 98 | 89 | 285 | 259 | |
Rest of World | 71 | 47 | 183 | 128 | |
506 | 357 | 1,364 | 1,013 | ||
Total Oncology | U.S. | 475 | 384 | 1,346 | 1,192 |
Europe | 236 | 275 | 779 | 821 | |
Rest of World | 149 | 129 | 418 | 381 | |
860 | 788 | 2,543 | 2,395 |
AmBisome U.S. | 3 | 2 | 14 | 15 |
Europe | 52 | 69 | 158 | 201 |
Rest of World | 44 | 52 | 175 | 175 |
99 | 123 | 347 | 391 | |
Other(5) U.S. | 36 | 34 | 97 | 125 |
Europe | 8 | 7 | 24 | 23 |
Rest of World | 25 | 20 | 57 | 55 |
68 | 61 | 177 | 204 | |
Total Other U.S. | 39 | 36 | 111 | 140 |
Europe | 59 | 76 | 181 | 225 |
Rest of World | 69 | 72 | 232 | 230 |
167 | 184 | 524 | 594 | |
Total product sales U.S. | 6,361 | 5,274 | 16,888 | 14,943 |
Europe | 1,058 | 1,144 | 3,350 | 3,395 |
Rest of World | 869 | 928 | 2,624 | 2,674 |
$ 8,289 $ 7,345 $ 22,862 $ 21,013
(1) Represents Gilead's revenue from cobicistat ("C"), FTC and TAF in Symtuza (darunavir/C/FTC/TAF), a fixed dose combination product commercialized by Janssen Sciences Ireland Unlimited Company.
(2) Includes Atripla, Bixlenvo, Complera/Eviplera, Emtriva, Stribild, Sunlenca, Truvada and Tybost.
(3) Includes Epclusa and the authorized generic version of Epclusa sold by Gilead's separate subsidiary, Asegua Therapeutics LLC ("Asegua").
(4) Includes ledipasvir/sofosbuvir (Harvoni and the authorized generic version of Harvoni sold by Asegua), Hepcludex, Sovaldi, Viread and Vosevi.
(5) Includes Cayston, Jyseleca, Letairis and Zydelig.
Forward-Looking StatementsStatements included in this press release that are not historical in nature are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Gilead cautions readers that forward-looking statements are subject to certain risks and uncertainties that could cause actual results to differ materially. These risks and uncertainties include those relating to: Gilead's ability to achieve its full year 2026 financial guidance and future projected financial results; impacts resulting from regulatory or legislative policies or processes, including the impact from pricing reform in the Inflation Reduction Act (such as Medicare Part D pricing reform and the Biktarvy Maximum Fair Price determination), the expiration of subsidies related to the Affordable Care Act, our most-favored-nation pricing agreement with the U.S. government and tariffs; Gilead's ability to make progress on any of its long-term ambitions or priorities laid out in its corporate strategy; Gilead's ability to accelerate or sustain revenues for its virology, oncology, inflammation and other programs; Gilead's ability to manage, execute and realize the potential benefits of acquisitions, collaborations or licensing arrangements, including the announced PepStar acquisition; the risk that Gilead's U.S. manufacturing and R&D investment may not achieve their intended benefits; patent protection and estimated loss of exclusivity for our products and product candidates; Gilead's ability to initiate, progress or complete clinical trials within currently anticipated timeframes or at all, the possibility of unfavorable results from ongoing and additional clinical trials, including those involving anito-cel, emvistegrast, lenacapavir and
HCXT-2001 (such as PURPOSE-365 and SWIFT), and the risk that safety and efficacy data from clinical trials may not warrant further development of Gilead's product candidates or the product candidates of Gilead's strategic partners; Gilead's ability to resolve the issues cited by the FDA in pending clinical holds to the satisfaction of the FDA and the risk that FDA may not remove such clinical holds, in whole or in part, in a timely manner or at all; Gilead's ability to submit new drug applications for new product candidates or expanded indications in the currently anticipated timelines; Gilead's ability to receive or maintain regulatory approvals in a timely manner or at all, and the risk that any such approvals, if granted, may be subject to significant limitations on use and may be subject to withdrawal or other adverse actions by the applicable regulatory authority; Gilead's ability to successfully commercialize its products; the risk of potential disruptions to the manufacturing and supply chain of Gilead's products; pricing and reimbursement pressures from government agencies and other third parties, including required rebates and other discounts; a larger than anticipated shift in payer mix to more highly discounted payer segments; market share and price erosion caused by the introduction of generic versions of Gilead products; the risk that physicians and patients may not see advantages of Gilead's products over other therapies, including Bixlenvo and Trodelvy; Gilead's ability to effectively manage, execute and realize the anticipated benefits of the access strategy relating to lenacapavir for HIV PrEP, including voluntary licensing arrangements and external partnerships relating to lenacapavir; and other risks identified from time to time in Gilead's reports filed with the SEC, including annual reports on Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K. In addition, Gilead makes estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses and related disclosures. Gilead bases its estimates on historical experience and on various other market specific and other relevant assumptions that it believes to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. There may be other factors of which Gilead is not currently aware that may affect matters discussed in the forward-looking statements and may also cause actual results to differ significantly from these estimates. Further, results for the quarter ended September 30, 2026 are not necessarily indicative of operating results for any future periods. Gilead directs readers to its press releases, annual reports on Form 10-K, quarterly reports on Form 10-Q and other subsequent disclosure documents filed with the SEC. Gilead claims the protection of the Safe Harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements.
The reader is cautioned that forward-looking statements are not guarantees of future performance and is cautioned not to place undue reliance on these forward-looking statements. All forward-looking statements are based on information currently available to Gilead and Gilead assumes no obligation to update or supplement any such forward-looking statements other than as required by law. Any forward-looking statements speak only as of the date hereof or as of the dates indicated in the statements.
Additional information is available on our Investor Relations website, https://investors.gilead.com. Among other things, an estimate of Acquired IPR&D expenses is expected to be made available on the Quarterly Results page within the first ten (10) days after the end of each quarter.
# # #
Gilead owns or has rights to various trademarks, copyrights and trade names used in its business, including the following: GILEAD®, GILEAD SCIENCES®, KITE®, AMBISOME®, ATRIPLA®, BIXLENVO™, BIKTARVY®, CAYSTON®, COMPLERA®, DESCOVY®, DESCOVY FOR PREP®, EMTRIVA®, EPCLUSA®, EVIPLERA®, GENVOYA®, HARVONI®, HEPCLUDEX®, JYSELECA®, LIVDELZI®/LYVDELZI®, LETAIRIS®, ODEFSEY®, SOVALDI®, STRIBILD®, SUNLENCA®, TECARTUS®, TRODELVY®, TRUVADA®, TRUVADA FOR PREP®, TYBOST®, VEKLURY®,
VEMLIDY®, VIREAD®, VOSEVI®, YESCARTA®, YEZTUGO®/YEYTUO® and ZYDELIG®. Other trademarks and trade names are the property of their respective owners.
For more information on Gilead Sciences, Inc., please visit https://www.gilead.com or call the Gilead Public Affairs Department at 1-800-GILEAD-5 (1-800-445-3235).

