8-K

Merck & Co., Inc. (MRK)

8-K 2025-02-04 For: 2025-02-04
View Original
Added on April 02, 2026

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C.  20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 OR 15(d) of

the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported) February 4, 2025 (February 4,2025 )

Merck & Co., Inc.

(Exact name of registrant as specified in its charter)

New Jersey<br> <br>(State or other jurisdiction<br> <br>of incorporation) 1-6571<br> <br>(Commission<br> <br>File Number) 22-1918501<br> <br>(I.R.S. Employer<br> <br>Identification No.)

126 East Lincoln Avenue, Rahway, NJ<br> <br>(Address of principal executive offices) 07065<br> <br>(Zip Code)

(Registrant’s telephone number, including area code)

(908) 740-4000

Not Applicable

(Former name, former address and former fiscal year, if changed since last report.)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

¨ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
¨ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
¨ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
¨ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company  ¨

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.  ¨

Securities registered pursuant to Section 12(b) of the Act:

Title of each class Trading Symbol(s) Name of each exchange on which registered
Common<br> Stock ($0.50 par value) MRK New York Stock Exchange
1.875% Notes due 2026 MRK/26 New York Stock Exchange
3.250% Notes due 2032 MRK/32 New York Stock Exchange
2.500% Notes due 2034 MRK/34 New York Stock Exchange
1.375% Notes due 2036 MRK 36A New York Stock Exchange
3.500% Notes due 2037 MRK/37 New York Stock Exchange
3.700% Notes due 2044 MRK/44 New York Stock Exchange
3.750% Notes due 2054 MRK/54 New York Stock Exchange

Item 2.02. Results of Operations and FinancialCondition.


The following information, including the exhibits hereto, is being furnished pursuant to this Item 2.02.

Incorporated by reference is a press release issued by Merck & Co., Inc. on February 4, 2025, regarding earnings for the fourth quarter and year end of 2024, attached as Exhibit 99.1. Also incorporated by reference is certain supplemental information not included in the press release, attached as Exhibit 99.2.

This information shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that Section, and is not incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.

Item 9.01. Financial Statements and Exhibits.


(d) Exhibits

Exhibit 99.1 Press release issued February 4, 2025, regarding earnings for the fourth quarter and year end of 2024
Exhibit 99.2 Certain supplemental information not included in the press release
Exhibit 104 Cover Page Interactive Data File (embedded within the Inline XBRL document)

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Merck & Co., Inc.
Date: February 4, 2025 By: /s/ Kelly E. W. Grez
Kelly E. W. Grez
Corporate Secretary

Exhibit 99.1

News Release

Merck Announces Fourth-Quarter and Full-Year2024 Financial Results

- Fourth-Quarter Worldwide Sales Were $15.6 Billion, an Increase of 7% From Fourth Quarter 2023; Excluding the Impact of Foreign Exchange,<br>Growth Was 9%
- Fourth-Quarter GAAP EPS Was $1.48; Non-GAAP EPS Was $1.72; GAAP and Non-GAAP EPS Include a Charge of $0.23 per Share Related<br>to Certain Business Development Transactions
--- ---
- Full-Year Worldwide Sales Were $64.2 Billion, an Increase of 7% From Full Year 2023; Excluding the Impact of Foreign Exchange, Growth<br>Was 10%
--- ---
o KEYTRUDA Sales Grew 18% to $29.5 Billion; Excluding the Impact of Foreign Exchange, Sales Grew 22%
--- ---
o WINREVAIR Sales Were $419 Million
--- ---
o Animal Health Sales Grew 4% to $5.9 Billion; Excluding the Impact of Foreign Exchange, Sales Grew 8%
--- ---
o GARDASIL/GARDASIL 9 Sales Declined 3% to $8.6 Billion; Excluding the Impact of Foreign Exchange, Sales Declined 2%
--- ---
- Full-Year 2024 GAAP EPS Was $6.74; Non-GAAP EPS Was $7.65; GAAP and Non-GAAP EPS Include a Net Charge of $1.28 per Share Related<br>to Certain Business Development Transactions
--- ---
- In the Fourth Quarter:
--- ---
o Announced Positive Topline Results From Pivotal Phase 3 Trial of Subcutaneous Pembrolizumab With Berahyaluronidase Alfa
--- ---
o Received FDA Acceptance of Biologics License Application for Clesrovimab, an Investigational Long-Acting Monoclonal Antibody Designed<br>to Protect Infants From RSV Disease During Their First RSV Season
--- ---
o Augmented Diverse Pipeline Through Exclusive Global Licenses With LaNova for MK-2010, an Investigational Anti-PD-1/VEGF Bispecific<br>Antibody, and With Hansoh for MK-4082, an Investigational Oral GLP-1 Receptor Agonist
--- ---
- Received Approval of GARDASIL for Males in China, in January 2025
--- ---
- Full-Year 2025 Financial Outlook
--- ---
o Anticipates Worldwide Sales To Be Between $64.1 Billion and $65.6 Billion
--- ---
o Expects Non-GAAP EPS To Be Between $8.88 and $9.03; Outlook Reflects a One-Time Charge of Approximately $0.09 per Share Related to<br>an Anticipated Milestone Payment to LaNova
--- ---

RAHWAY, N.J., Feb. 4, 2025 – Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced financial results for the fourth quarter of 2024.

- 2 -

“We delivered strong growth in 2024, reflecting demand for our innovative portfolio, including for KEYTRUDA, which continues to benefit more patients with cancer globally, the successful launch of WINREVAIR and strong performance of our Animal Health business,” said Robert M. Davis, chairman and chief executive officer, Merck. "We’re continuing to progress our pipeline, advance key clinical programs and augment our pipeline through promising business development. Our business remains well positioned thanks to the dedication of our talented global team, and I am more confident than ever in our long-term growth potential.”

Financial Summary

Fourth<br> Quarter Year<br> Ended
$<br> in millions, except<br> EPS amounts 2024 2023 Change Change<br> <br> Ex-Exchange Dec. 31,<br><br> 2024 Dec. 31,<br><br> 2023 Change Change<br> <br> Ex-Exchange
Sales $ 15,624 $ 14,630 7 % 9 % $ 64,168 $ 60,115 7 % 10 %
GAAP<br> net income (loss)^1^ 3,743 (1,226 ) N/M N/M 17,117 365 N/M N/M
Non-GAAP<br> net income that excludes certain items^1,2*^ 4,372 66 N/M N/M 19,444 3,837 N/M N/M
GAAP<br> EPS 1.48 (0.48 ) N/M N/M 6.74 0.14 N/M N/M
Non-GAAP<br> EPS that excludes certain items^2*^ 1.72 0.03 N/M N/M 7.65 1.51 N/M N/M

*Refer to table on page 9.

N/M - not meaningful

Generally Accepted Accounting Principles (GAAP) earnings per share (EPS) assuming dilution was $1.48 for the fourth quarter and $6.74 for the full year of 2024. Non-GAAP EPS was $1.72 for the fourth quarter and $7.65 for the full year of 2024. GAAP and non-GAAP EPS in the fourth quarter of 2024 include a charge of $0.23 per share related to the execution of licensing agreements with LaNova Medicines Ltd. (LaNova) and Hansoh Pharma (Hansoh). GAAP loss per share and non-GAAP EPS in the fourth quarter of 2023 include a charge of $1.69 per share related to a collaboration with Daiichi Sankyo. GAAP and non-GAAP EPS for the full years of 2024 and 2023 include charges of $1.28 and $6.21 per share, respectively, related to certain collaborations, licensing agreements and asset acquisitions.

^1^ Net income (loss) attributable to Merck & Co., Inc.

^2^ Merck is providing certain 2024 and 2023 non-GAAP information that excludes certain items because of the nature of these items and the impact they have on the analysis of underlying business performance and trends. Management believes that providing this information enhances investors’ understanding of the company’s results because management uses non-GAAP results to assess performance. Management uses non-GAAP measures internally for planning and forecasting purposes and to measure the performance of the company along with other metrics. In addition, annual employee compensation, including senior management’s compensation, is derived in part using a non-GAAP pretax income metric. This information should be considered in addition to, but not as a substitute for or superior to, information prepared in accordance with GAAP. For a description of the non-GAAP adjustments, see Table 2a attached to this release.

- 3 -

Non-GAAP EPS excludes acquisition- and divestiture-related costs, costs related to restructuring programs, and income and losses from investments in equity securities. Non-GAAP EPS in the fourth quarter and full year of 2024 also exclude a benefit due to a reduction in reserves for unrecognized income tax benefits resulting from the expiration of the statute of limitations for assessments related to certain federal tax return years. Non-GAAP EPS for the full year of 2023 also excludes a charge related to settlements with certain plaintiffs in the Zetia antitrust litigation.

Fourth-Quarter Sales Performance

The following table reflects sales of the company’s top products and significant performance drivers.

Fourth Quarter
in millions 2024 2023 Change Change Ex-Exchange Commentary
Total Sales 15,624 $ 14,630 7 % 9 % The negative impact of foreign exchange was primarily due to devaluation of Argentine peso, which was largely offset by inflation-related price increases, consistent with practice in that market.
Pharmaceutical 14,042 13,141 7 % 8 % Increase driven by growth in oncology and cardiovascular, partially offset by declines in diabetes, vaccines, immunology and virology.
KEYTRUDA 7,836 6,608 19 % 21 % Growth driven by continued strong global demand from metastatic indications, including increased uptake in bladder and endometrial cancers, as well as increased global uptake in earlier-stage indications, including triple-negative breast cancer and non-small cell lung cancer (NSCLC). The negative impact of foreign exchange was primarily due to devaluation of Argentine peso, which was largely offset by inflation-related price increases.
GARDASIL/GARDASIL 9 1,550 1,871 -17 % -18 % Decline primarily due to lower demand in China, partially offset by higher demand in most international regions, particularly in Japan.
PROQUAD, M-M-R II and VARIVAX 594 545 9 % 9 % Growth primarily due to higher pricing in the U.S. and higher tenders in certain international markets, partially offset by lower demand in the U.S.
JANUVIA/JANUMET 487 787 -38 % -36 % Decline primarily due to lower pricing in the U.S., as well as ongoing generic competition in many international markets and supply constraints in China.
BRIDION 449 429 5 % 5 % Growth primarily due to higher demand in the U.S., partially offset by generic competition in certain international markets, particularly in Japan and Europe.
Lynparza* 365 315 16 % 18 % Growth primarily due to higher global demand.
Lenvima* 255 226 13 % 14 % Growth primarily due to timing of shipments in certain international markets.
PREVYMIS 215 175 23 % 23 % Growth primarily due to higher demand in most markets, particularly in the U.S.
WEVAIR 200 - - - Represents continued uptake since second-quarter launch in the U.S.

All values are in US Dollars.

- 4 -
Fourth Quarter
$ in millions 2024 2023 Change Change Ex-Exchange Commentary
VAXNEUVANCE 161 176 -9 % -9 % Decline primarily driven by lower demand in the U.S. due to competition, partially offset by continued uptake from launches in Europe and the Asia Pacific region.
WELIREG 160 72 122 % 123 % Growth primarily driven by higher demand in the U.S., largely attributable to ongoing uptake of a new indication.
SIMPONI - 171 N/M N/M Marketing rights in former Merck territories reverted to Johnson & Johnson on Oct. 1, 2024.
Animal Health 1,397 1,278 9 % 13 % Growth primarily driven by higher pricing for both Livestock and Companion Animal product portfolios, as well as sales related to July 2024 acquisition of Elanco aqua business and higher demand for Livestock products. Approximately 3 percentage points of the negative impact of foreign exchange were due to devaluation of Argentine peso, which were largely offset by inflation-related price increases.
Livestock 889 808 10 % 14 % Growth primarily driven by higher demand for poultry products, sales related to acquisition of Elanco aqua business, as well as higher pricing across the portfolio.
Companion Animal 508 470 8 % 10 % Growth primarily driven by higher pricing across the product portfolio. Sales of BRAVECTO were $209 million and $197 million in current and prior year quarters, respectively, which represented growth of 6%, or 10% excluding impact of foreign exchange.
Other Revenues** 185 211 -13 % 3 % Decline primarily due to impact of revenue-hedging activities and lower revenues from third-party manufacturing arrangements, partially offset by payments received for out-licensing arrangements and higher royalty income.

*Alliance revenue for this product represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs.

**Other revenues are comprised primarily of revenues from third-party manufacturing arrangements and miscellaneous corporate revenues, including revenue-hedging activities.

N/M – not meaningful

- 5 -

Full-Year Sales Performance

The following table reflects sales of the company’s top products and significant performance drivers.

in millions Dec. 31, 2023 Change Change <br> Ex-Exchange
Total Sales 64,168 $ 60,115 7 % 10 %
Pharmaceutical 57,400 53,583 7 % 10 %
KEYTRUDA 29,482 25,011 18 % 22 %
GARDASIL/GARDASIL 9 8,583 8,886 -3 % -2 %
PROQUAD, M-M-R II and VARIVAX 2,485 2,368 5 % 5 %
JANUVIA/JANUMET 2,268 3,366 -33 % -29 %
BRIDION 1,764 1,842 -4 % -3 %
Lynparza* 1,311 1,199 9 % 11 %
Lenvima* 1,010 960 5 % 6 %
LAGEVRIO 964 1,428 -33 % -28 %
VAXNEUVANCE 808 665 22 % 23 %
PREVYMIS 785 605 30 % 33 %
ROTATEQ 711 769 -8 % -7 %
SIMPONI** 543 710 -24 % -23 %
WELIREG 509 218 133 % 133 %
WEVAIR 419 - - -
Animal Health 5,877 5,625 4 % 8 %
Livestock 3,462 3,337 4 % 9 %
Companion Animal 2,415 2,288 6 % 7 %
Other Revenues*** 891 907 -2 % 4 %

All values are in Indian Rupees.

*Alliance revenue for this product represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs.

**Marketing rights in former Merck territories reverted to Johnson & Johnson on Oct. 1, 2024.

***Other revenues are comprised primarily of revenues from third-party manufacturing arrangements and miscellaneous corporate revenues, including revenue-hedging activities.

Full-year 2024 pharmaceutical sales grew 7% to $57.4 billion. Excluding the unfavorable impact of foreign exchange, pharmaceutical sales grew 10%. Approximately 2 percentage points of the negative impact of foreign exchange were due to devaluation of the Argentine peso, which were largely offset by inflation-related price increases, consistent with practice in that market. Pharmaceutical sales growth was primarily driven by higher sales in oncology, particularly KEYTRUDA and WELIREG, as well as increased alliance revenue from Reblozyl and Lynparza. Higher sales in the cardiovascular franchise, reflecting the successful launch of WINREVAIR, as well as higher sales of certain hospital acute care products, particularly PREVYMIS, also drove revenue growth in 2024. Pharmaceutical sales growth in 2024 was partially offset by lower sales of JANUVIA and JANUMET, primarily reflecting lower pricing in the U.S. and generic competition in many international markets, lower sales of the COVID-19 medication LAGEVRIO, lower sales of GARDASIL/GARDASIL 9 and lower sales of SIMPONI and REMICADE, reflecting the transfer of marketing rights in former Merck territories back to Johnson & Johnson.

Full-year 2024 Animal Health sales grew 4% to $5.9 billion. Excluding the unfavorable impact of foreign exchange, Animal Health sales grew 8%. Approximately 2 percentage points of the negative impact of foreign exchange were due to devaluation of the Argentine peso, which were largely offset by inflation-related price increases, consistent with practice in that market. Full-year sales growth was primarily driven by higher pricing across both the Companion Animal and Livestock product portfolios, and higher demand for poultry and swine products, as well as sales related to the acquisition of the Elanco aqua business. Sales of BRAVECTO were $1.1 billion in 2024, which represented growth of 6%, or 8% excluding the impact of foreign exchange.

- 6 -

Fourth-Quarter and Full-Year Expense, EPS and Related Information

The table below presents selected expense information.

$ in millions GAAP Acquisition- and Divestiture- Related Costs^3^ Restructuring<br> Costs (Income)<br> Loss From<br> Investments<br> in Equity<br> Securities Non- GAAP^2^
Fourth Quarter 2024
Cost of sales $ 3,828 $ 701 $ 121 $ - $ 3,006
Selling, general and administrative 2,864 29 16 - 2,819
Research and development 4,585 12 (1 ) - 4,574
Restructuring costs 51 - 51 - -
Other (income) expense, net 126 (31 ) - 152 5
Fourth Quarter 2023
Cost of sales $ 3,911 $ 454 $ 117 $ - $ 3,340
Selling, general and administrative 2,804 24 29 - 2,751
Research and development 9,628 790 - - 8,838
Restructuring costs 255 - 255 - -
Other (income) expense, net 78 (35 ) - (61 ) 174
$ in millions GAAP Acquisition- and Divestiture- Related Costs^3^ Restructuring<br> Costs (Income)<br> Loss From<br> Investments<br> in Equity<br> Securities Certain<br> Other<br> Items Non- GAAP^2^
--- --- --- --- --- --- --- --- --- --- --- --- --- --- --- ---
Year Ended December 31, 2024
Cost of sales $ 15,193 $ 2,409 $ 495 $ - $ - $ 12,289
Selling, general and administrative 10,816 117 83 - - 10,616
Research and development 17,938 72 1 - - 17,865
Restructuring costs 309 - 309 - - -
Other (income) expense, net (24 ) (79 ) - 45 - 10
Year Ended December 31, 2023
Cost of sales $ 16,126 $ 2,018 $ 211 $ - $ - $ 13,897
Selling, general and administrative 10,504 86 122 - - 10,296
Research and development 30,531 819 1 - - 29,711
Restructuring costs 599 - 599 - - -
Other (income) expense, net 466 (47 ) - (279 ) 573 219

^3^ Reflects expenses related to business combinations, including the amortization of intangible assets, intangible asset impairment charges, and expense or income related to changes in the estimated fair value measurement of liabilities for contingent consideration. Also includes integration, transaction and certain other costs associated with acquisitions and divestitures, as well as amortization of intangible assets related to collaborations and licensing arrangements.

- 7 -

GAAP Expense, EPS and Related Information

Gross margin was 75.5% for the fourth quarter of 2024 compared with 73.3% for the fourth quarter of 2023. The increase was primarily due to the favorable effects of product mix (including lower royalty rates related to KEYTRUDA and GARDASIL/GARDASIL 9) and foreign exchange, partially offset by higher manufacturing-related costs (including inventory write-offs) and higher amortization of intangible assets. Gross margin was 76.3% for the full year of 2024 compared with 73.2% for the full year of 2023. The increase was primarily due to the favorable effects of product mix (including lower royalty rates related to KEYTRUDA and GARDASIL/GARDASIL 9) and foreign exchange, partially offset by higher amortization of intangible assets, as well as higher restructuring costs (primarily reflecting asset impairment charges) and higher manufacturing-related costs (including inventory write-offs).

Selling, general and administrative (SG&A) expenses were $2.9 billion in the fourth quarter of 2024, an increase of 2% compared with the fourth quarter of 2023. The increase was primarily due to higher promotional and selling costs, partially offset by the favorable impact of foreign exchange and lower restructuring costs. Full-year 2024 SG&A expenses were $10.8 billion, an increase of 3% compared with full-year 2023. The increase was primarily due to higher administrative, promotional, selling and acquisition-related costs, partially offset by the favorable impact of foreign exchange and lower restructuring costs.

Research and development (R&D) expenses were $4.6 billion in the fourth quarter of 2024, a decrease of 52% compared with the fourth quarter of 2023. R&D expenses were $17.9 billion for the full year of 2024, a decrease of 41% compared with the full year of 2023. The declines in both the fourth quarter and full year of 2024 were primarily due to lower charges for business development activity, lower intangible asset impairment charges, and the favorable impact of foreign exchange, partially offset by increased compensation and benefit costs and higher clinical development spending.

Other (income) expense, net, was $126 million of expense in the fourth quarter of 2024 compared with $78 million of expense in the fourth quarter of 2023. The unfavorability was primarily due to net losses from investments in equity securities compared with net income from investments in equity securities in the prior year quarter, partially offset by lower foreign exchange losses and lower net interest expense. Other (income) expense, net, was $24 million of income in the full year of 2024 compared with $466 million of expense in the full year of 2023, primarily due to a $572.5 million charge in 2023 related to settlements with certain plaintiffs in the Zetia antitrust litigation. The favorability was also due to $170 million of income related to the expansion of an existing development and commercialization agreement with Daiichi Sankyo, as well as lower foreign exchange losses in 2024. Other (income) expense, net, in the full year of 2024 was unfavorably affected by lower net income from investments in equity securities and higher net interest expense compared with 2023.

The effective tax rates of 10.2% and 14.1% for the fourth quarter and full year of 2024, respectively, include a 6.2 percentage point favorable impact and a 2.6 percentage point favorable impact, respectively, due to a reduction in reserves for unrecognized income tax benefits, resulting from the expiration of the statute of limitations for assessments related to certain federal tax return years.

- 8 -

GAAP EPS was $1.48 for the fourth quarter of 2024 compared with a loss per share of $0.48 for the fourth quarter of 2023, primarily driven by lower charges for business development transactions, operational strength in the business, lower intangible asset impairment charges, and a benefit from the expiration of the statute of limitations for assessments related to the 2020 federal tax return year. GAAP EPS was $6.74 for the full year of 2024 compared with EPS of $0.14 for the full year of 2023. The increase was primarily driven by lower charges for business development transactions, operational strength in the business, lower intangible asset impairment charges, a benefit from the expiration of the statute of limitations for the 2020 and 2019 federal tax return years, and a charge in the prior year for settlements with certain plaintiffs in the Zetia antitrust litigation, partially offset by the unfavorable effect of foreign exchange.

Non-GAAP Expense, EPS and Related Information

Non-GAAP gross margin was 80.8% for the fourth quarter of 2024 compared with 77.2% for the fourth quarter of 2023. Non-GAAP gross margin was 80.8% for the full year of 2024 compared with 76.9% for the full year of 2023. The non-GAAP gross margin improvements in both the fourth quarter and full year of 2024 were primarily due to the favorable effects of product mix (including lower royalty rates related to KEYTRUDA and GARDASIL/GARDASIL 9) and foreign exchange, partially offset by higher manufacturing-related costs (including inventory write-offs).

Non-GAAP SG&A expenses were $2.8 billion in the fourth quarter of 2024, an increase of 2% compared with the fourth quarter of 2023. Non-GAAP SG&A expenses were $10.6 billion for the full year of 2024, an increase of 3% compared with the full year of 2023. The increases were primarily due to higher promotional and selling costs and, for the full year, higher administrative costs, partially offset by the favorable impact of foreign exchange.

Non-GAAP R&D expenses were $4.6 billion in the fourth quarter of 2024, a decrease of 48% compared with the fourth quarter of 2023. Non-GAAP R&D expenses were $17.9 billion for the full year of 2024, a decrease of 40% compared with the full year of 2023. The declines in both the fourth quarter and full year of 2024 were primarily due to lower charges for business development activity and the favorable impact of foreign exchange, partially offset by increased compensation and benefit costs and higher clinical development spending.

Non-GAAP other (income) expense, net, was $5 million of expense in the fourth quarter of 2024 compared with $174 million of expense in the fourth quarter of 2023. The favorability was primarily due to lower foreign exchange losses and lower net interest expense. Non-GAAP other (income) expense, net, was $10 million of expense in the full year of 2024 compared with $219 million of expense in the full year of 2023. The favorability was primarily due to $170 million of income related to the expansion of an existing development and commercialization agreement with Daiichi Sankyo, as well as lower foreign exchange losses in 2024, partially offset by higher net interest expense.

- 9 -

The non-GAAP effective tax rate was 16.2% for the fourth quarter and 16.8% for the full year of 2024.

Non-GAAP EPS was $1.72 for the fourth quarter of 2024 compared with $0.03 for the fourth quarter of 2023. Non-GAAP EPS was $7.65 for the full year of 2024 compared with EPS of $1.51 for the full year of 2023. The increase in both periods was primarily driven by lower charges for business development transactions and operational strength in the business. The unfavorable effect of foreign exchange partially offset the increase in the full year.

A reconciliation of GAAP to non-GAAP net income (loss) and earnings (loss) per share is provided in the table that follows.

Fourth Quarter Year Ended
$ in millions, except EPS amounts 2024 2023 Dec. 31,<br> 2024 Dec. 31,<br> 2023
EPS
GAAP EPS $ 1.48 $ (0.48 ) $ 6.74 $ 0.14
Difference 0.24 0.51 0.91 1.37
Non-GAAP EPS that excludes items listed below^2^ $ 1.72 $ 0.03 $ 7.65 $ 1.51
Net Income (Loss)
GAAP net income (loss)^1^ $ 3,743 $ (1,226 ) $ 17,117 $ 365
Difference 629 1,292 2,327 3,472
Non-GAAP net income that excludes items listed below^1,2^ $ 4,372 $ 66 $ 19,444 $ 3,837
Excluded Items:
Acquisition- and divestiture-related costs^3^ $ 711 $ 1,233 $ 2,519 $ 2,876
Restructuring costs 187 401 888 933
Loss (income) from investments in equity securities 152 (61 ) 45 (279 )
Charge for Zetia antitrust litigation settlements - - - 573
Decrease to net income/increase to net loss before taxes 1,050 1,573 3,452 4,103
Estimated income tax (benefit) expense^4^ (421 ) (281 ) (1,125 ) (631 )
Decrease to net income/increase to net loss $ 629 $ 1,292 $ 2,327 $ 3,472

Pipeline and Portfolio Highlights

Merck made important advancements in its broad, diverse pipeline, meeting significant regulatory and clinical milestones throughout the fourth quarter.

In oncology, Merck announced positive topline results from the pivotal Phase 3 MK-3475A-D77 trial evaluating the noninferiority of subcutaneous pembrolizumab and berahyaluronidase alfa, in combination with chemotherapy, versus intravenous (IV) KEYTRUDA administered with chemotherapy, for the first-line treatment of adult patients with metastatic NSCLC. Subcutaneous pembrolizumab and berahyaluronidase alfa has the potential to improve the patient experience and increase access for patients and health care providers compared to IV administration.

^4^ Includes the estimated tax impacts on the reconciling items based on applying the statutory rate of the originating territory of the non-GAAP adjustments, as well as a $260 million benefit and a $519 million benefit in the fourth quarter and full year of 2024, respectively, due to reductions in reserves for unrecognized income tax benefits resulting from the expiration of the statute of limitations for assessments related to certain federal tax return years. The benefit recognized in the fourth quarter of 2024 relates to the 2020 federal tax return year and the benefit for the full year of 2024 relates to both the 2020 and 2019 federal tax return years.

- 10 -

Merck presented new data across multiple hematologic malignancies at the American Society of Hematology Annual Meeting and Exposition in December 2024, including promising Phase 2 data for its investigational antibody-drug conjugate zilovertamab vedotin for the treatment of patients with previously untreated diffuse large B-cell lymphoma. With more than 20 abstracts presented, the data showcased Merck’s continued progress in advancing clinical research for its expanding and diverse hematology pipeline.

Merck also achieved several key regulatory milestones in the U.S., Europe, Japan and China. Highlights include the U.S. Food and Drug Administration (FDA) granting Breakthrough Therapy designation to sacituzumab tirumotecan (sac-TMT) for the treatment of certain patients with previously treated advanced or metastatic nonsquamous NSCLC with epidermal growth factor receptor (EGFR) mutations. Additionally, Merck received new approvals for KEYTRUDA-based regimens in Japan and China, as well as for WELIREG and Lynparza in China.

In vaccines and infectious diseases, the FDA accepted the Biologics License Application (BLA) for clesrovimab, an investigational prophylactic long-acting monoclonal antibody designed to protect infants from respiratory syncytial virus (RSV) disease during their first RSV season and set a Prescription Drug User Fee Act (PDUFA) date of June 10, 2025. This regulatory milestone marks important progress toward having clesrovimab available in time for the 2025-26 RSV season. The filing was based on results from the pivotal Phase 2b/3 study of clesrovimab in infants for the prevention of RSV that was presented at ID Week 2024. In addition, Merck announced topline results from two pivotal Phase 3 trials of the investigational, once-daily, oral, two-drug, single-tablet regimen of doravirine/islatravir (DOR/ISL) in adults with virologically suppressed HIV-1 infection, in line with Merck’s commitment to help address the needs of people living with HIV.

In January 2025, Merck also received expanded approval in China for GARDASIL. It is now the first HPV vaccine approved in China for the prevention of certain HPV-related cancers and diseases in males 9-26 years of age. In addition, the European Union’s (EU) Committee for Medicinal Products for Human Use (CHMP) recommended the approval of CAPVAXIVE for pneumococcal vaccination in adults, with a final decision for EU approval expected in the second quarter of 2025.

In cardiovascular disease, Merck announced positive topline results from the Phase 3 ZENITH study, evaluating WINREVAIR in adults with pulmonary arterial hypertension (PAH) with World Health Organization (WHO) Group 1 functional class (FC) III or IV at high risk of mortality. Based on the positive results of an interim analysis, an independent data monitoring committee recommended that the study be stopped early due to overwhelming efficacy. In addition, in January 2025, Merck announced the Phase 3 HYPERION study evaluating WINREVAIR in newly diagnosed adults with PAH with FC II or III at intermediate or high risk of disease progression was also stopped early based on the positive results from the interim analysis of the ZENITH trial and a review of the totality of data from the WINREVAIR clinical program to date. All participants in both the ZENITH and HYPERION studies will be offered the opportunity to receive WINREVAIR as part of the open-label, long-term extension study, SOTERIA.

- 11 -

Merck continued to execute on its business development strategy. The company announced the closing of an exclusive global license for MK-2010, a novel investigational PD-1/VEGF bispecific antibody from LaNova. Merck also entered into an exclusive global license agreement with Hansoh to evaluate MK-4082, an investigational preclinical oral small molecule glucagon-like peptide (GLP-1) receptor agonist.

Notable recent news releases on Merck’s pipeline and portfolio are provided in the table that follows.

Oncology FDA Granted Breakthrough Therapy Designation to sac-TMT for the Treatment of Certain Patients With Previously Treated Advanced or Metastatic Nonsquamous NSCLC With EGFR Mutations (Read Announcement)
FDA Granted Priority Review to Merck’s Application for WELIREG for the Treatment of Patients With Advanced Pheochromocytoma and Paraganglioma (Read Announcement)
Merck Received Positive EU CHMP Opinion for WELIREG as Treatment for Adult Patients With Certain Types of Von Hippel-Lindau (VHL) Disease-Associated Tumors and for Certain Previously Treated Adult Patients With Advanced RCC, Based on Results From Phase 2 LITESPARK-004 and Phase 3 LITESPARK-005 Trials (Read Announcement)
Merck Received Positive EU CHMP Opinion for KEYTRUDA Plus Chemotherapy as First-Line Treatment for Adult Patients With Unresectable Non-Epithelioid Malignant Pleural Mesothelioma, Based on Results From Phase 2/3 IND.227/KEYNOTE-483 Trial (Read Announcement)
KEYTRUDA Approved in China in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy After Surgery as Adjuvant Treatment for Patients With Resectable Stage II, IIIA or IIIB NSCLC, Based on Results From Phase 3 KEYNOTE-671 Trial (Read Announcement)
WELIREG Approved in China for Treatment of Adult Patients With Certain Types of VHL Disease-Associated Tumors, Based on Results From Phase 2 LITESPARK-004 Trial (Read Announcement)
Merck Announced Phase 3 MK-3475A-D77 Trial of Subcutaneous Pembrolizumab With Berahyaluronidase Alfa Met Primary Endpoints (Read Announcement)
Merck Announced Phase 3 KEYLYNK-001 Trial Met Primary Endpoint of Progression-Free Survival in Patients With Advanced Epithelial Ovarian Cancer (Read Announcement)
Lynparza Demonstrated Clinically Meaningful Prolonged Survival Benefit in Early Breast Cancer, Based on Results From Phase 3 OlympiA Trial (Read Announcement)
Investigational Zilovertamab Vedotin in Combination With R-CHP Demonstrated Complete Response Rate of 100% at 1.75 MG/KG Dose in Previously Untreated Patients With Diffuse Large B-Cell Lymphoma, Based on Results From Phase 2 WaveLINE-007 Trial (Read Announcement)
- 12 -
Vaccines Merck Announced FDA Acceptance of BLA for Clesrovimab (MK-1654), an Investigational Long-Acting Monoclonal Antibody Designed to Protect Infants From RSV Disease During Their First RSV Season; FDA Set PDUFA Date of June 10, 2025 (Read Announcement)
Merck Received Expanded Approval of GARDASIL for Males in China (Read Announcement)
Merck Received Positive EU CHMP Opinion for CAPVAXIVE for Pneumococcal Vaccination in Adults (Read Announcement)
Merck Presented New Data From GARDASIL 9 Studies Reinforcing Importance of Gender-Neutral HPV Vaccination in Adults Up to Age 45 at International Papillomavirus Conference 2024 (Read Announcement)
Cardiovascular Merck Announced Pivotal Phase 3 ZENITH Trial Evaluating WINREVAIR Met Primary Endpoint at Interim Analysis (Read Announcement)
Merck Announced Decision to Stop Phase 3 HYPERION Trial Evaluating WINREVAIR Early and Move to Final Analysis (Read Announcement)
Infectious Diseases Merck Announced Topline Results From Pivotal Phase 3 Trials Evaluating Investigational, Once-Daily, Oral, Two-Drug, Single-Tablet Regimen of Doravirine/Islatravir (DOR/ISL) for the Treatment of Adults With Virologically Suppressed HIV-1 Infection (Read Announcement)

Full-Year 2025 Financial Outlook

The following table summarizes the company’s full-year financial outlook.

Full Year 2025
Sales^*^ $64.1 billion to $65.6 billion
Non-GAAP Gross margin^2^ Approximately 82.5%
Non-GAAP Operating expenses^2**^ $25.4 billion to $26.4 billion
Non-GAAP Other (income) expense, net^2^ $300 million to $400 million expense
Non-GAAP Effective tax rate^2^ 16.0% to 17.0%
Non-GAAP EPS^2***^ $8.88 to $9.03
Share count (assuming dilution) Approximately 2.53 billion

*The company does not have any non-GAAP adjustments to sales.

**Includes $300 million for an anticipated milestone payment to LaNova associated with the technology transfer for MK-2010 expected to be completed in 2025. Outlook does not assume any additional significant potential business development transactions.

***Includes expected one-time charge of approximately $0.09 per share related to the $300 million milestone payment to LaNova upon completion of the technology transfer for MK-2010.

Merck has not provided a reconciliation of forward-looking non-GAAP gross margin, non-GAAP operating expenses, non-GAAP other (income) expense, net, non-GAAP effective tax rate and non-GAAP EPS to the most directly comparable GAAP measures, given it cannot predict with reasonable certainty the amounts necessary for such a reconciliation, including intangible asset impairment charges, legal settlements, and income and losses from investments in equity securities either owned directly or through ownership interests in investment funds, without unreasonable effort. These items are inherently difficult to forecast and could have a significant impact on the company’s future GAAP results.

Merck anticipates full-year 2025 sales to be between $64.1 billion and $65.6 billion, including a negative impact of foreign exchange of approximately 2% at mid-January 2025 exchange rates. This sales range reflects a decision to temporarily pause shipments of GARDASIL/GARDASIL 9 into China beginning February 2025 through at least mid-year.

- 13 -

Merck’s full-year non-GAAP effective income tax rate is expected to be between 16.0% and 17.0%.

Merck expects full-year 2025 non-GAAP EPS to be between $8.88 and $9.03, including a negative impact of foreign exchange of approximately $0.35 per share. This range includes an expected one-time charge of $300 million, or approximately $0.09 per share, related to a milestone payment to LaNova, which will be recognized upon completion of the technology transfer for MK-2010. In 2024, non-GAAP EPS of $7.65 was negatively impacted by a net charge of $1.28 per share related to certain asset acquisitions, licensing agreements and collaborations.

Consistent with past practice, the financial outlook does not assume additional significant potential business development transactions.

Earnings Conference Call

Investors, journalists and the general public may access a live audio webcast of the earnings conference call on Tuesday, Feb. 4, at 9 a.m. ET via this weblink. A replay of the webcast, along with the sales and earnings news release, supplemental financial disclosures, and slides highlighting the results, will be available at www.merck.com.

All participants may join the call by dialing (800) 369-3351 (U.S. and Canada Toll-Free) or (517) 308-9448 and using the access code 9818590.

About Merck

At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com and connect with us on X (formerly Twitter), Facebook, Instagram, YouTube and LinkedIn.

Forward-Looking Statement of Merck & Co., Inc., Rahway,N.J., USA

This news release of Merck & Co., Inc., Rahway, N.J., USA (the “company”) includes “forward-looking statements” within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. These statements are based upon the current beliefs and expectations of the company’s management and are subject to significant risks and uncertainties. There can be no guarantees with respect to pipeline candidates that the candidates will receive the necessary regulatory approvals or that they will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements.

- 14 -

Risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and health care legislation in the United States and internationally; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the company’s ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the company’s patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions.

The company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in the company’s Annual Report on Form 10-K for the year ended December 31, 2023 and the company’s other filings with the Securities and Exchange Commission (SEC) available at the SEC’s Internet site (www.sec.gov).

Appendix

Generic product names are provided below.

Pharmaceutical

BRIDION (sugammadex)

CAPVAXIVE (Pneumococcal 21-valent Conjugate Vaccine)

GARDASIL (Human Papillomavirus Quadrivalent [Types 6, 11,16 and 18] Vaccine, Recombinant)

GARDASIL 9 (Human Papillomavirus 9-valent Vaccine, Recombinant)

JANUMET (sitagliptin and metformin HCl)

JANUVIA (sitagliptin)

KEYTRUDA (pembrolizumab)

LAGEVRIO (molnupiravir)

Lenvima (lenvatinib)

Lynparza (olaparib)

M-M-R II (Measles, Mumps and Rubella Virus Vaccine Live)

PREVYMIS (letermovir)

PROQUAD (Measles, Mumps, Rubella and Varicella Virus VaccineLive)

Reblozyl (luspatercept)

REMICADE (infliximab)

ROTATEQ (Rotavirus Vaccine, Live, Oral, Pentavalent)

SIMPONI (golimumab)

VARIVAX (Varicella Virus Vaccine Live)

- 15 -

VAXNEUVANCE (Pneumococcal 15-valent Conjugate Vaccine)

WELIREG (belzutifan)

WINREVAIR*(sotatercept-csrk)*

Animal Health

BRAVECTO (fluralaner)

Media Contacts: Investor Contacts:
Robert Josephson<br><br> <br>(203) 914-2372<br><br> <br>robert.josephson@merck.com<br><br> <br><br><br> <br>Michael Levey<br><br> <br>(215) 872-1462<br><br> <br>michael.levey@merck.com Peter Dannenbaum<br><br> <br>(732) 594-1579<br><br> <br>peter.dannenbaum@merck.com<br><br> <br><br><br> <br>Steven Graziano<br><br> <br>(732) 594-1583<br><br> <br>steven.graziano@merck.com

MERCK & CO., INC.

CONSOLIDATEDSTATEMENT OF OPERATIONS - GAAP

(AMOUNTSIN MILLIONS, EXCEPT PER SHARE FIGURES)

(UNAUDITED)

Table1

GAAP % Change GAAP % Change
4Q24 4Q23 Full Year 2024 Full Year 2023
Sales $ 15,624 $ 14,630 7 % $ 64,168 $ 60,115 7 %
Costs, Expenses and Other
Cost of sales 3,828 3,911 -2 % 15,193 16,126 -6 %
Selling, general and administrative 2,864 2,804 2 % 10,816 10,504 3 %
Research and development 4,585 9,628 -52 % 17,938 30,531 -41 %
Restructuring costs 51 255 -80 % 309 599 -48 %
Other (income) expense, net 126 78 62 % (24 ) 466 *
Income (Loss) Before Taxes 4,170 (2,046 ) * 19,936 1,889 *
Income Tax Provision (Benefit) 425 (821 ) 2,803 1,512
Net Income (Loss) 3,745 (1,225 ) * 17,133 377 *
Less: Net Income Attributable to Noncontrolling Interests 2 1 16 12
Net Income (Loss) Attributable to Merck & Co.,<br> Inc. $ 3,743 $ (1,226 ) * $ 17,117 $ 365 *
Earnings (Loss) per Common Share Assuming Dilution<br> ^(1)^ $ 1.48 $ (0.48 ) * $ 6.74 $ 0.14 *
Average Shares Outstanding Assuming Dilution ^(1)^ 2,537 2,533 2,541 2,547
Tax Rate 10.2 % 40.1 % 14.1 % 80.0 %
* 100% or greater

^(1)^ Because the company recorded a net loss in the fourth quarter of 2023, no potential dilutive common shares were used in the computation of loss per common share assuming dilution as the effect would have been anti-dilutive.

MERCK & CO., INC. FOURTH QUARTER AND FULL YEAR 2024 GAAP TO NON-GAAP RECONCILIATION(AMOUNTS IN MILLIONS, EXCEPT PER SHARE FIGURES) (UNAUDITED) Table 2a

**** GAAP **** Acquisition and Divestiture-Related Costs ^(1)^ **** Restructuring Costs ^(2)^ **** (Income) Loss from Investments in Equity Securities **** Certain Other Items **** Adjustment Subtotal **** Non-GAAP ****
Fourth Quarter
Cost of sales $ 3,828 701 121 822 $ 3,006
Selling, general and administrative 2,864 29 16 45 2,819
Research and development 4,585 12 (1 ) 11 4,574
Restructuring costs 51 51 51
Other (income) expense, net 126 (31 ) 152 121 5
Income Before Taxes 4,170 (711 ) (187 ) (152 ) (1,050 ) 5,220
Income Tax Provision (Benefit) 425 (111 )^(3)^ (17 )^(3)^ (33 )^(3)^ (260 )^(4)^ (421 ) 846
Net Income 3,745 (600 ) (170 ) (119 ) 260 (629 ) 4,374
Net Income Attributable to Merck & Co., Inc. 3,743 (600 ) (170 ) (119 ) 260 (629 ) 4,372
Earnings per Common Share Assuming Dilution $ 1.48 (0.23 ) (0.07 ) (0.04 ) 0.10 (0.24 ) $ 1.72
Tax Rate 10.2 % 16.2 %
Full Year
Cost of sales $ 15,193 2,409 495 2,904 $ 12,289
Selling, general and administrative 10,816 117 83 200 10,616
Research and development 17,938 72 1 73 17,865
Restructuring costs 309 309 309
Other (income) expense, net (24 ) (79 ) 45 (34 ) 10
Income Before Taxes 19,936 (2,519 ) (888 ) (45 ) (3,452 ) 23,388
Income Tax Provision (Benefit) 2,803 (461 )^(3)^ (135 )^(3)^ (10 )^(3)^ (519 )^(4)^ (1,125 ) 3,928
Net Income 17,133 (2,058 ) (753 ) (35 ) 519 (2,327 ) 19,460
Net Income Attributable to Merck & Co., Inc. 17,117 (2,058 ) (753 ) (35 ) 519 (2,327 ) 19,444
Earnings per Common Share Assuming Dilution $ 6.74 (0.81 ) (0.30 ) (0.01 ) 0.21 (0.91 ) $ 7.65
Tax Rate 14.1 % 16.8 %

Only the line items that are affected by non-GAAP adjustments are shown.

Merck is providing certain non-GAAP information that excludes certain items because of the nature of these items and the impact they have on the analysis of underlying business performance and trends. Management believes that providing non-GAAP information enhances investors’ understanding of the company’s results because management uses non-GAAP measures to assess performance. Management uses non-GAAP measures internally for planning and forecasting purposes and to measure the performance of the company along with other metrics. In addition, annual employee compensation, including senior management’s compensation, is derived in part using a non-GAAP pretax income metric. The non-GAAP information presented should be considered in addition to, but not as a substitute for or superior to, information prepared in accordance with GAAP.

^^

^(1)^Amounts included in cost of sales primarily reflect expenses for the amortization of intangible assets. Amounts included in selling, general and administrative expenses reflect integration, transaction and certain other costs related to acquisitions and divestitures. Amounts included in research and development expenses primarily reflect the amortization of intangible assets. Additionally, research and development expenses for the full year includes Animal Health intangible asset impairment charges. Amounts included in other (income) expense, net, primarily reflect royalty income and a decrease in the estimated fair value measurement of liabilities for contingent consideration related to the prior termination of the Sanofi-Pasteur MSD joint venture.

^(2)^Amounts primarily include employee separation costs, accelerated depreciation and asset impairments associated with facilities to be closed or divested related to activities under the company's formal restructuring programs.

^(3)^ Represents the estimated tax impacts on the reconciling items based on applying the statutory rate of the originating territory of the non-GAAP adjustments.

^^

^(4)^ Represents benefits recorded in the fourth quarter and full year due to reductions in reserves for unrecognized income tax benefits resulting from the expiration of the statute of limitations for assessments related to federal income tax return years. The benefit recognized in the fourth quarter relates to the 2020 federal tax return year and the benefit recognized for the full year relates to both the 2020 and 2019 federal tax return years.

MERCK & CO., INC.FRANCHISE / KEY PRODUCT SALES(AMOUNTS IN MILLIONS) (UNAUDITED) Table 3

2024 2023 4<br> Q Full Year
1Q 2Q 3Q 4Q Full Year 1Q 2Q 3Q 4Q Full Year Nom % Ex-Exch % Nom % Ex-Exch %
TOTAL SALES ^(1)^ $ 15,775 $ 16,112 $ 16,657 $ 15,624 $ 64,168 $ 14,487 $ 15,035 $ 15,962 $ 14,630 $ 60,115 7 9 7 10
PHARMACEUTICAL 14,006 14,408 14,943 14,042 57,400 12,721 13,457 14,263 13,141 53,583 7 8 7 10
Oncology
Keytruda 6,947 7,270 7,429 7,836 29,482 5,795 6,271 6,338 6,608 25,011 19 21 18 22
Alliance<br> Revenue – Lynparza ^(2)^ 292 317 337 365 1,311 275 310 299 315 1,199 16 18 9 11
Alliance<br> Revenue – Lenvima ^(2)^ 255 249 251 255 1,010 232 242 260 226 960 13 14 5 6
Welireg 85 126 139 160 509 42 50 54 72 218 122 123 133 133
Alliance<br> Revenue – Reblozyl ^(3)^ 71 90 100 110 371 43 47 52 70 212 58 58 75 75
Vaccines ^(4)^
Gardasil/Gardasil 9 2,249 2,478 2,306 1,550 8,583 1,972 2,458 2,585 1,871 8,886 -17 -18 -3 -2
ProQuad/M-M-R<br> II/Varivax 570 617 703 594 2,485 528 582 713 545 2,368 9 9 5 5
Vaxneuvance 219 189 239 161 808 106 168 214 176 665 -9 -9 22 23
RotaTeq 216 163 193 139 711 297 131 156 185 769 -25 -25 -8 -7
Pneumovax 23 61 59 68 74 263 96 92 140 85 412 -12 -12 -36 -34
Hospital<br> Acute Care
Bridion 440 455 420 449 1,764 487 502 424 429 1,842 5 5 -4 -3
Prevymis 174 188 208 215 785 129 143 157 175 605 23 23 30 33
Dificid 73 92 96 79 340 65 76 74 87 302 -9 -9 13 13
Zerbaxa 56 62 64 70 252 50 54 53 61 218 14 16 16 18
Noxafil 56 45 41 36 177 60 55 51 46 213 -23 -17 -17 -8
Cardiovascular
Winrevair 70 149 200 419 - - - -
Alliance<br> Revenue - Adempas/Verquvo ^(5)^ 98 106 102 109 415 99 68 92 108 367 1 1 13 13
Adempas<br> ^(6)^ 70 72 72 73 287 59 65 65 66 255 11 9 12 14
Virology
Lagevrio 350 110 383 121 964 392 203 640 193 1,428 -37 -37 -33 -28
Isentress/Isentress<br> HD 111 89 102 92 394 123 136 119 105 483 -13 -7 -18 -14
Delstrigo 56 60 65 69 249 44 50 54 54 201 28 29 24 26
Pifeltro 42 39 42 40 163 34 38 37 33 142 20 20 15 15
Neuroscience
Belsomra 46 53 78 45 222 56 63 58 54 231 -17 -17 -4 1
Immunology
Simponi 184 172 189 543 180 180 179 171 710 N/M N/M -24 -23
Remicade 39 35 41 114 51 48 45 43 187 N/M N/M -39 -36
Diabetes ^(7)^
Januvia 419 405 278 232 1,334 551 511 581 547 2,189 -58 -56 -39 -36
Janumet 251 224 204 255 935 329 354 255 240 1,177 7 11 -21 -16
Other Pharmaceutical ^(8)^ 576 573 644 713 2,510 626 560 568 576 2,333 25 25 8 10
ANIMAL<br> HEALTH 1,511 1,482 1,487 1,397 5,877 1,491 1,456 1,400 1,278 5,625 9 13 4 8
Livestock 850 837 886 889 3,462 849 807 874 808 3,337 10 14 4 9
Companion<br> Animal 661 645 601 508 2,415 642 649 526 470 2,288 8 10 6 7
Other Revenues ^(9)^ 258 222 227 185 891 275 122 299 211 907 -13 3 -2 4

N/M - Not Meaningful

Sum of quarterly amounts may not equal year-to-date amounts due to rounding.

^(1)^ Only select products are shown.

^(2)^ Alliance Revenue represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs.

^(3)^ Alliance Revenue represents royalties.

^(4)^ Total Vaccines sales were $3,424 million, $3,656 million, $3,675 million and $2,693 million in the first, second, third and fourth quarter of 2024, respectively, and $3,133 million, $3,557 million, $4,002 million and $2,962 million in the first, second, third and fourth quarter of 2023, respectively.

^(5)^ Alliance Revenue represents Merck's share of profits from sales in Bayer's marketing territories, which are product sales net of cost of sales and commercialization costs.

^(6)^ Net product sales in Merck's marketing territories.

^(7)^ Total Diabetes sales were $745 million, $715 million, $592 million and $546 million in the first, second, third and fourth quarter of 2024, respectively, and $950 million, $951 million, $924 million and $876 million in the first, second, third and fourth quarter of 2023, respectively.

^(8)^ Includes Pharmaceutical products not individually shown above.

^(9)^ Other Revenues are comprised primarily of revenues from third-party manufacturing arrangements and miscellaneous corporate revenues, including revenue-hedging activities. Other Revenues related to the receipt of upfront and milestone payments for out-licensed products were $61 million, $15 million, $15 million and $15 million in the first, second, third and fourth quarter of 2024, respectively, and $51 million, $3 million and $65 million in the first, second and third quarter of 2023, respectively.

Exhibit 99.2

MERCK & CO., INC.

CONSOLIDATEDSTATEMENT OF OPERATIONS - GAAP

(AMOUNTSIN MILLIONS, EXCEPT PER SHARE FIGURES)

(UNAUDITED)

Table1a

2024 2023 % Change
1Q 2Q 3Q 4Q Full Year 1Q 2Q 3Q 4Q Full Year 4Q Full Year
Sales $ 15,775 $ 16,112 $ 16,657 $ 15,624 $ 64,168 $ 14,487 $ 15,035 $ 15,962 $ 14,630 $ 60,115 7 % 7 %
Costs, Expenses<br> and Other
Cost of sales 3,540 3,745 4,080 3,828 15,193 3,926 4,024 4,264 3,911 16,126 -2 % -6 %
Selling, general and administrative 2,483 2,739 2,731 2,864 10,816 2,479 2,702 2,519 2,804 10,504 2 % 3 %
Research and development 3,992 3,500 5,862 4,585 17,938 4,276 13,321 3,307 9,628 30,531 -52 % -41 %
Restructuring costs 123 80 56 51 309 67 151 126 255 599 -80 % -48 %
Other (income) expense, net (33 ) 42 (162 ) 126 (24 ) 89 172 126 78 466 62 % *
Income (Loss) Before Taxes 5,670 6,006 4,090 4,170 19,936 3,650 (5,335 ) 5,620 (2,046 ) 1,889 * *
Income Tax Provision (Benefit) 903 545 929 425 2,803 825 637 870 (821 ) 1,512
Net Income (Loss) 4,767 5,461 3,161 3,745 17,133 2,825 (5,972 ) 4,750 (1,225 ) 377 * *
Less: Net Income Attributable<br> to Noncontrolling Interests 5 6 4 2 16 4 3 5 1 12
Net Income (Loss) Attributable<br> to Merck & Co., Inc. $ 4,762 $ 5,455 $ 3,157 $ 3,743 $ 17,117 $ 2,821 $ (5,975 ) $ 4,745 $ (1,226 ) $ 365 * *
Earnings<br> (Loss) per Common Share Assuming Dilution ^(1)^ $ 1.87 $ 2.14 $ 1.24 $ 1.48 $ 6.74 $ 1.11 $ (2.35 ) $ 1.86 $ (0.48 ) $ 0.14 * *
Average<br> Shares Outstanding Assuming Dilution ^(1)^ 2,544 2,544 2,541 2,537 2,541 2,551 2,539 2,546 2,533 2,547
Tax Rate 15.9 % 9.1 % 22.7 % 10.2 % 14.1 % 22.6 % -11.9 % 15.5 % 40.1 % 80.0 %

* 100% or greater

Sum of quarterly amounts may not equal year-to-date amounts due to rounding.

^(1)^Because the company recorded a net loss in the second quarter and the fourth quarter of 2023, no potential dilutive common shares were used in the computation of loss per common share assuming dilution as the effect would have been anti-dilutive.

MERCK & CO., INC.FOURTH QUARTER AND FULL YEAR 2023 GAAP TO NON-GAAP RECONCILIATION (AMOUNTS IN MILLIONS, EXCEPT PER SHARE FIGURES) (UNAUDITED) Table 2b

GAAP Acquisition and Divestiture- Related Costs ^(1)^ Restructuring Costs ^(2)^ (Income)<br> Loss from<br><br> Investments in Equity<br><br> Securities Certain<br> Other Items Adjustment<br> Subtotal Non-GAAP
Fourth Quarter
Cost of sales $ 3,911 454 117 571 $ 3,340
Selling, general and administrative 2,804 24 29 53 2,751
Research and development 9,628 790 790 8,838
Restructuring costs 255 255 255
Other (income) expense, net 78 (35 ) (61 ) (96 ) 174
Loss Before Taxes (2,046 ) (1,233 ) (401 ) 61 (1,573 ) (473 )
Income Tax Provision (Benefit) (821 ) (227 )^(4)^ (67 )^(4)^ 13 ^(4)^ (281 ) (540 )
Net (Loss) Income (1,225 ) (1,006 ) (334 ) 48 (1,292 ) 67
Net (Loss) Income Attributable to Merck & Co., Inc. (1,226 ) (1,006 ) (334 ) 48 (1,292 ) 66
(Loss)<br> Earnings per Common Share Assuming Dilution ^(5)^ $ (0.48 ) (0.40 ) (0.13 ) 0.02 (0.51 ) $ 0.03
Tax Rate 40.1 % 114.2 %
Full Year
Cost of sales $ 16,126 2,018 211 2,229 $ 13,897
Selling, general and administrative 10,504 86 122 208 10,296
Research and development 30,531 819 1 820 29,711
Restructuring costs 599 599 599
Other (income) expense, net 466 (47 ) (279 ) 573 ^(3)^ 247 219
Income Before Taxes 1,889 (2,876 ) (933 ) 279 (573 ) (4,103 ) 5,992
Income Tax Provision (Benefit) 1,512 (476 )^(4)^ (155 )^(4)^ 60 ^(4)^ (60 )^(4)^ (631 ) 2,143
Net Income 377 (2,400 ) (778 ) 219 (513 ) (3,472 ) 3,849
Net Income Attributable to Merck & Co., Inc. 365 (2,400 ) (778 ) 219 (513 ) (3,472 ) 3,837
Earnings per Common Share Assuming Dilution $ 0.14 (0.94 ) (0.31 ) 0.08 (0.20 ) (1.37 ) $ 1.51
Tax Rate 80.0 % 35.8 %
Only<br> the line items that are affected by non-GAAP adjustments are shown.
---
Merck is providing<br> certain non-GAAP information that excludes certain items because of the nature of these items and the impact they have on the analysis<br> of underlying business performance and trends. Management believes that providing non-GAAP information enhances investors’<br> understanding of the company’s results because management uses non-GAAP measures to assess performance. Management uses non-GAAP<br> measures internally for planning and forecasting purposes and to measure the performance of the company along with other metrics.<br> In addition, annual employee compensation, including senior management’s compensation, is derived in part using a non-GAAP<br> pretax income metric. The non-GAAP information presented should be considered in addition to, but not as a substitute for or superior<br> to, information prepared in accordance with GAAP.
^(1)^Amounts<br> included in cost of sales primarily reflect expenses for the amortization of intangible assets. Amounts included in selling, general<br> and administrative expenses reflect integration, transaction and certain other costs related to acquisitions and divestitures. Amounts<br> included in research and development expenses primarily reflect a $779 million in-process research and development (IPR&D) impairment<br> charge related to gefapixant and expenses for the amortization of intangible assets. Amounts included in other (income) expense,<br> net, primarily reflect royalty income related to the prior termination of the Sanofi-Pasteur MSD joint venture. Additionally, other<br> (income) expense, net, for the full year includes a $37 million loss on the sale of a business.
^(2)^Amounts<br> primarily include employee separation costs and accelerated depreciation associated with facilities to be closed or divested related<br> to activities under the company's formal restructuring programs.
^(3)^<br> Reflects a charge related to settlements with certain plaintiffs in the Zetia antitrust litigation.
^(4)^<br> Represents the estimated tax impacts on the reconciling items based on applying the statutory rate of the originating territory of<br> the non-GAAP adjustments.
^(5)^<br> Because the company recorded a net loss in the fourth quarter of 2023, no potential dilutive common shares were used in the computation<br> of loss per common share assuming dilution as the effect would have been anti-dilutive.

MERCK & CO., INC. FRANCHISE / KEY PRODUCT SALES FOURTH QUARTER 2024 (AMOUNTS IN MILLIONS) (UNAUDITED) Table 3a

Global U.S. International
4Q<br> 2024 4Q<br> 2023 %<br> Change 4Q<br> 2024 4Q<br> 2023 %<br> Change 4Q<br> 2024 4Q<br> 2023 %<br> Change
TOTAL SALES ^(1)^ $ 15,624 $ 14,630 7 $ 8,188 $ 7,088 16 $ 7,436 $ 7,542 -1
PHARMACEUTICAL 14,042 13,141 7 7,728 6,698 15 6,314 6,443 -2
Oncology
Keytruda 7,836 6,608 19 4,841 3,972 22 2,996 2,636 14
Alliance<br> Revenue – Lynparza ^(2)^ 365 315 16 177 168 5 187 147 28
Alliance<br> Revenue – Lenvima ^(2)^ 255 226 13 182 181 1 73 45 63
Welireg 160 72 122 146 68 114 14 4 *
Alliance<br> Revenue – Reblozyl ^(3)^ 110 70 58 88 60 47 22 10 124
Vaccines ^(4)^
Gardasil/Gardasil 9 1,550 1,871 -17 380 365 4 1,170 1,506 -22
ProQuad/M-M-R<br> II/Varivax 594 545 9 419 402 4 175 143 23
Vaxneuvance 161 176 -9 64 138 -53 96 38 153
RotaTeq 139 185 -25 84 112 -25 55 73 -25
Pneumovax 23 74 85 -12 19 22 -13 55 62 -12
Hospital<br> Acute Care
Bridion 449 429 5 382 315 21 67 113 -41
Prevymis 215 175 23 106 78 36 109 98 12
Dificid 79 87 -9 72 75 -4 7 12 -42
Zerbaxa 70 61 14 40 33 23 30 28 4
Noxafil 36 46 -23 -2 4 -149 37 43 -12
Cardiovascular
Winrevair 200 - 192 - 9 -
Alliance<br> Revenue - Adempas/Verquvo ^(5)^ 109 108 1 105 102 3 5 6 -27
Adempas<br> ^(6)^ 73 66 11 73 66 11
Virology
Lagevrio 121 193 -37 32 10 * 88 183 -52
Isentress/Isentress<br> HD 92 105 -13 38 50 -23 53 56 -4
Delstrigo 69 54 28 14 12 19 55 42 30
Pifeltro 40 33 20 26 23 16 13 10 29
Neuroscience
Belsomra 45 54 -17 19 21 -12 26 33 -20
Immunology
Simponi 171 N/M 171 N/M
Remicade 43 N/M 43 N/M
Diabetes ^(7)^
Januvia 232 547 -58 41 309 -87 191 239 -20
Janumet 255 240 7 91 41 122 164 198 -17
Other Pharmaceutical ^(8)^ 713 576 25 172 137 26 544 438 24
ANIMAL<br> HEALTH 1,397 1,278 9 444 387 15 953 891 7
Livestock 889 808 10 203 158 28 686 649 6
Companion<br> Animal 508 470 8 241 229 5 267 242 11
Other Revenues ^(9)^ 185 211 -13 16 3 * 169 208 -19

*200% or greater

N/M - Not Meaningful
Sum of U.S. plus international may not equal global due to rounding.
^(1)^ Only select products are shown.
^(2)^ Alliance Revenue represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs.
^(3)^ Alliance Revenue represents royalties.
^(4)^ Total Vaccines sales were $2,693 million and $2,962 million on a global basis in the fourth quarter of 2024 and 2023, respectively.
^(5)^ Alliance Revenue represents Merck's share of profits from sales in Bayer's marketing territories, which are product sales net of cost of sales and commercialization costs.
^(6)^ Net product sales in Merck's marketing territories.
^(7)^ Total Diabetes sales were $546 million and $876 million on a global basis in the fourth quarter of 2024 and 2023, respectively.
^(8)^ Includes Pharmaceutical products not individually shown above.
^(9)^ Other Revenues are comprised primarily of revenues from third-party manufacturing arrangements and miscellaneous corporate revenues, including revenue-hedging activities. Other Revenues related to the receipt of upfront and milestone payments for out-licensed products were $15 million on a global basis in the fourth quarter of 2024.

MERCK & CO., INC. FRANCHISE / KEY PRODUCT SALES FULL YEAR 2024(AMOUNTS IN MILLIONS) (UNAUDITED) Table 3b

Global U.S. International
FullYear<br><br> 2024 Full<br> Year<br><br> 2023 %<br> Change Full<br> Year<br><br> 2024 Full<br> Year<br><br> 2023 %<br> Change Full<br> Year<br><br> 2024 Full<br> Year<br><br> 2023 %<br> Change
TOTAL SALES ^(1)^ $ 64,168 $ 60,115 7 $ 32,277 $ 28,480 13 $ 31,891 $ 31,635 1
PHARMACEUTICAL 57,400 53,583 7 30,290 26,539 14 27,110 27,044 -
Oncology
Keytruda 29,482 25,011 18 17,872 15,114 18 11,610 9,897 17
Alliance<br> Revenue – Lynparza ^(2)^ 1,311 1,199 9 626 607 3 685 592 16
Alliance<br> Revenue – Lenvima ^(2)^ 1,010 960 5 705 657 7 305 303 1
Welireg 509 218 133 466 209 123 43 10 *
Alliance<br> Revenue – Reblozyl ^(3)^ 371 212 75 303 168 80 68 43 56
Vaccines ^(4)^
Gardasil/Gardasil 9 8,583 8,886 -3 2,425 2,083 16 6,158 6,803 -9
ProQuad/M-M-R II/Varivax 2,485 2,368 5 1,919 1,837 4 566 531 7
Vaxneuvance 808 665 22 461 561 -18 347 103 *
RotaTeq 711 769 -8 472 493 -4 239 276 -13
Pneumovax 23 263 412 -36 56 127 -56 207 285 -27
Hospital Acute Care
Bridion 1,764 1,842 -4 1,401 1,156 21 363 686 -47
Prevymis 785 605 30 371 264 41 414 341 21
Dificid 340 302 13 303 274 10 37 28 34
Zerbaxa 252 218 16 146 119 23 106 100 7
Noxafil 177 213 -17 7 32 -78 170 181 -6
Cardiovascular
Winrevair 419 - 408 - 11 -
Alliance<br> Revenue - Adempas/Verquvo ^(5)^ 415 367 13 388 350 11 27 16 65
Adempas<br> ^(6)^ 287 255 12 287 255 12
Virology
Lagevrio 964 1,428 -33 176 10 * 787 1,418 -44
Isentress/Isentress HD 394 483 -18 185 215 -14 209 268 -22
Delstrigo 249 201 24 56 49 14 193 152 27
Pifeltro 163 142 15 113 101 12 50 41 22
Neuroscience
Belsomra 222 231 -4 72 81 -11 150 150 -
Immunology
Simponi 543 710 -24 543 710 -24
Remicade 114 187 -39 114 187 -39
Diabetes ^(7)^
Januvia 1,334 2,189 -39 469 1,151 -59 865 1,039 -17
Janumet 935 1,177 -21 161 223 -28 774 954 -19
Other Pharmaceutical ^(8)^ 2,510 2,333 8 729 658 11 1,782 1,675 6
ANIMAL HEALTH 5,877 5,625 4 1,861 1,804 3 4,016 3,821 5
Livestock 3,462 3,337 4 732 700 5 2,729 2,637 3
Companion Animal 2,415 2,288 6 1,129 1,104 2 1,287 1,184 9
Other Revenues ^(9)^ 891 907 -2 126 137 -8 765 770 -1
*200% or greater
---
Sum of U.S. plus international may not equal global due to<br> rounding.
^(1)^Only select products are shown.
^(2)^Alliance Revenue represents Merck’s share of profits, which are product sales net of cost of sales and commercialization<br> costs.
^(3)^Alliance Revenue represents royalties.
^(4)^Total Vaccines sales were $13,448 million and $13,654 million on a global basis for December YTD 2024 and 2023, respectively.
^(5)^Alliance Revenue represents Merck's share of profits from sales in Bayer's marketing territories, which are product sales net<br> of cost of sales and commercialization costs.
^(6)^Net product sales in Merck's marketing territories.
^(7)^Total Diabetes sales were $2,599 million and $3,701 million on a global basis for December YTD 2024 and 2023, respectively.
^(8)^Includes Pharmaceutical products not individually shown above.
^(9)^Other Revenues are comprised primarily of revenues from third-party manufacturing arrangements and miscellaneous corporate<br> revenues, including revenue-hedging activities. Other Revenues related to the receipt of upfront and milestone payments for out-licensed<br> products were $106 million and $118 million on a global basis for December YTD 2024 and 2023, respectively.

MERCK & CO., INC.PHARMACEUTICAL GEOGRAPHIC SALES (AMOUNTS IN MILLIONS) (UNAUDITED) Table 3c

2024 2023 %<br> Change
1Q 2Q 3Q 4Q Full<br> Year 1Q 2Q 3Q 4Q Full<br> Year 4Q Full<br> Year
TOTAL<br> PHARMACEUTICAL $ 14,006 $ 14,408 $ 14,943 $ 14,042 $ 57,400 $ 12,721 $ 13,457 $ 14,263 $ 13,141 $ 53,583 7 7
United<br> States 6,936 7,399 8,227 7,728 30,290 6,117 6,570 7,153 6,698 26,539 15 14
%<br> Pharmaceutical Sales 49.5 % 51.4 % 55.1 % 55.0 % 52.8 % 48.1 % 48.8 % 50.1 % 51.0 % 49.5 %
Europe ^(1)^ 2,555 2,572 2,620 2,498 10,246 2,326 2,401 2,497 2,491 9,715 - 5
%<br> Pharmaceutical Sales 18.2 % 17.9 % 17.5 % 17.8 % 17.9 % 18.3 % 17.8 % 17.5 % 19.0 % 18.1 %
China 1,744 1,790 996 864 5,394 1,694 1,887 1,674 1,456 6,710 -41 -20
%<br> Pharmaceutical Sales 12.5 % 12.4 % 6.7 % 6.2 % 9.4 % 13.3 % 14.0 % 11.7 % 11.1 % 12.5 %
Japan 802 664 919 813 3,199 737 652 1,062 629 3,081 29 4
%<br> Pharmaceutical Sales 5.7 % 4.6 % 6.2 % 5.8 % 5.6 % 5.8 % 4.8 % 7.4 % 4.8 % 5.7 %
Latin<br> America 601 661 730 680 2,672 470 566 696 596 2,328 14 15
%<br> Pharmaceutical Sales 4.3 % 4.6 % 4.9 % 4.8 % 4.7 % 3.7 % 4.2 % 4.9 % 4.5 % 4.3 %
Asia<br> Pacific (other than China and Japan) 580 595 669 612 2,457 703 705 636 616 2,661 -1 -8
%<br> Pharmaceutical Sales 4.1 % 4.1 % 4.5 % 4.4 % 4.3 % 5.5 % 5.2 % 4.5 % 4.7 % 5.0 %
Eastern<br> Europe/Middle East/Africa 395 353 400 348 1,495 381 370 301 299 1,351 16 11
%<br> Pharmaceutical Sales 2.8 % 2.4 % 2.7 % 2.5 % 2.6 % 3.0 % 2.7 % 2.1 % 2.3 % 2.5 %
Canada 138 143 133 144 558 141 127 133 138 540 4 3
%<br> Pharmaceutical Sales 1.0 % 1.0 % 0.9 % 1.0 % 1.0 % 1.1 % 0.9 % 0.9 % 1.1 % 1.0 %
Other 255 231 249 355 1,089 152 179 111 218 658 63 66
%<br> Pharmaceutical Sales 1.9 % 1.6 % 1.5 % 2.5 % 1.7 % 1.2 % 1.6 % 0.9 % 1.5 % 1.4 %

Sum of quarterly amounts may not equal year-to-date amounts due to rounding.

^(1)^Europe represents all European Union countries, the European Union accession markets and the United Kingdom.

MERCK & CO., INC. OTHER (INCOME) EXPENSE, NET - GAAP (AMOUNTS IN MILLIONS) (UNAUDITED) Table 4

OTHER (INCOME) EXPENSE, NET
4Q24 4Q23 Full Year<br><br> 2024 Full Year<br><br> 2023
Interest income $ (146 ) $ (70 ) $ (415 ) $ (365 )
Interest expense 328 310 1,271 1,146
Exchange losses 49 162 227 370
Loss<br> (income) from investments in equity securities, net ^(1)^ 156 (99 ) (14 ) (340 )
Net periodic defined benefit plan (credit) cost other than<br> service cost (157 ) (134 ) (633 ) (498 )
Other, net (104 ) (91 ) (460 ) 153
Total $ 126 $ 78 $ (24 ) $ 466

^(1)^Includes net realized and unrealized gains and losses from investments in equity securities either owned directly or through ownership interests in investment funds. Unrealized gains and losses from investments that are directly owned are determined at the end of the reporting period, while gains and losses from ownership interests in investment funds are accounted for on a one quarter lag.