STOCK TITAN

AbbVie completes $10.9B Apogee Therapeutics deal

AbbVie closes its $10.9 billion Apogee deal, adds key immunology assets and long-acting antibodies while reaffirming 2026 EPS guidance despite near-term dilution.

(High)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

AbbVie Inc. (ABBV) announced completion of its acquisition of Apogee Therapeutics, Inc. for $135.11 per share in cash, implying a total equity value of approximately $10.9 billion, adding late-stage and early-stage immunology assets focused on atopic dermatitis, asthma and COPD. Apogee is now part of AbbVie.

Apogee’s lead drug candidate zumilokibart (APG777), a half‑life extended IL‑13 monoclonal antibody for atopic dermatitis, showed in a Phase 2 trial that about two‑thirds of patients achieved significant skin clearance at 16 weeks, with sustained control enabling quarterly or twice‑yearly dosing, and a favorable safety profile. Combination candidate APG273, which includes an antibody blocking TSLP, is being developed for asthma with data supporting long‑acting dosing.

AbbVie expects the acquisition to reduce adjusted diluted EPS by $0.14 in 2026 and about $0.46 in 2027, with accretion beginning in 2032, but is reaffirming its 2026 full‑year adjusted diluted EPS guidance range of $13.87–$14.07 and third‑quarter 2026 adjusted diluted EPS guidance of $3.84–$3.88. The 2026 EPS outlook includes an unfavorable $0.58 per share impact from acquired IPR&D and milestones recorded through the second quarter.

Positive

  • Completed $10.9 billion Apogee acquisition adds late-stage immunology assets, including zumilokibart for atopic dermatitis and APG273 for asthma, expanding AbbVie’s pipeline in large inflammatory markets.
  • Reaffirmation of 2026 full-year adjusted diluted EPS guidance of $13.87–$14.07 and third-quarter 2026 guidance of $3.84–$3.88 indicates the company is maintaining its earnings outlook despite acquisition-related dilution.
  • Phase 2 data for zumilokibart showed approximately two-thirds of patients achieved significant skin clearance at 16 weeks with notable itch reduction, supporting potential best-in-category positioning and infrequent maintenance dosing.

Negative

  • AbbVie expects the Apogee acquisition to negatively impact adjusted diluted EPS by $0.14 in 2026 and approximately $0.46 in 2027, creating a meaningful near-term earnings headwind until accretion begins in 2032.
  • The 2026 adjusted diluted EPS outlook already includes an unfavorable $0.58 per share impact from acquired IPR&D and milestones expense through the second quarter, highlighting the earnings drag from R&D investments.

Filing Explained

AbbVie’s reaffirmed third-quarter 2026 adjusted diluted EPS guidance of $3.84–$3.88 excludes any acquired IPR&D and milestone expense incurred during that quarter, so the range does not incorporate costs the company says cannot be reliably forecast.

Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Apogee purchase price per share $135.11 per share Cash consideration paid to Apogee shareholders at closing
Total Apogee equity value $10.9 billion Aggregate equity value of AbbVie’s acquisition of Apogee
2026 adjusted diluted EPS guidance range $13.87–$14.07 Reaffirmed full-year 2026 adjusted diluted EPS guidance
Q3 2026 adjusted diluted EPS guidance range $3.84–$3.88 Reaffirmed third-quarter 2026 adjusted diluted EPS guidance
EPS dilution from Apogee in 2026 $0.14 per share Expected negative impact on 2026 adjusted diluted EPS (partial year)
EPS dilution from Apogee in 2027 $0.46 per share Expected negative impact on 2027 adjusted diluted EPS
Acquired IPR&D and milestones EPS impact 2026 $0.58 per share Unfavorable impact included in 2026 adjusted diluted EPS guidance through Q2
Immunology patient reach Over 1,000,000 patients Patients worldwide treated with AbbVie’s immunology medicines
adjusted diluted EPS financial
"AbbVie reaffirms previously issued 2026 full-year adjusted diluted EPS guidance range"
Adjusted diluted EPS is a company’s profit per share after adding back or removing one-time items (like restructuring costs or gains) and dividing by the number of shares including potential shares from options and convertible securities. Investors use it as a cleaner view of ongoing earnings—like looking at a car’s regular fuel efficiency rather than a trip boosted by downhill coasting—to judge underlying performance and compare companies without temporary distortions.
acquired IPR&D financial
"includes an unfavorable impact of $0.58 per share related to acquired IPR&D"
Acquired IPR&D means the research and development projects a company buys from another party before they are completed, including experimental drugs, prototypes, or unfinalized technologies. It matters to investors because these unfinished assets are treated differently on financial statements—often recorded as an immediate expense or separate intangible—so they can affect reported earnings, future revenue potential, and the buyer’s valuation similar to buying a recipe that still needs testing.
in-process research and development financial
"acquired in-process research and development assets, including zumilokibart (APG777)"
Unfinished research and development work—such as drug candidates, prototypes, or process designs—that a company is actively developing but has not yet completed or commercialized. Investors care because it represents potential future products or technologies (like a half-built prototype) whose value is uncertain; it affects how acquisitions are priced, how future profits and costs are forecast, and can be written down if the project fails.
thymic stromal lymphopoietin (TSLP) medical
"APG273, a potential best-in-category long-acting combination targeting IL-13 and thymic stromal lymphopoietin (TSLP)"
Thymic stromal lymphopoietin (TSLP) is a small signaling protein produced by certain cells that tells the immune system to start or heighten inflammatory responses, especially in the airways and skin. Investors care because TSLP is a clear drug target and potential biomarker—blocking or measuring it can change how chronic allergic, asthma, and other inflammatory conditions are treated, affecting drug development paths, regulatory reviews, and commercial prospects much like flipping a thermostat can change a whole room’s climate.
type 2 inflammation medical
"Zumilokibart targets IL-13, a critical cytokine in type 2 inflammation"
An immune response driven by a specific set of cells and signaling molecules that causes allergic-type inflammation in tissues such as the lungs, skin and sinuses; think of it as the body’s alarm system stuck in the “allergy” mode. It matters to investors because drugs that reduce or block this pathway can treat common, chronic conditions (asthma, eczema, chronic sinusitis) and represent large, targeted markets with potential for premium-priced, specialty medicines.
monoclonal antibody medical
"zumilokibart, is a late-stage, half-life extended monoclonal antibody targeting IL-13"
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
2026 adjusted diluted EPS guidance range $13.87–$14.07 Guidance reaffirmed; includes $0.14 per share dilutive impact from Apogee acquisition
Q3 2026 adjusted diluted EPS guidance range $3.84–$3.88 Guidance reaffirmed; excludes any future acquired IPR&D and milestones in the quarter
Apogee acquisition EPS impact 2026 $0.14 per share dilution Expected negative impact on 2026 adjusted diluted EPS from the acquisition
Apogee acquisition EPS impact 2027 $0.46 per share dilution Expected negative impact on 2027 adjusted diluted EPS from the acquisition
Acquired IPR&D and milestones EPS impact 2026 $0.58 per share unfavorable impact Impact from acquired IPR&D and milestones expense incurred through Q2 2026 included in guidance
Guidance

AbbVie reaffirms its 2026 full-year adjusted diluted EPS guidance of $13.87–$14.07 and third-quarter 2026 adjusted diluted EPS guidance of $3.84–$3.88, while incorporating a $0.14 per share dilutive impact from the Apogee acquisition and a $0.58 per share unfavorable impact from acquired IPR&D and milestones through Q2.

FAQ

What acquisition did AbbVie (ABBV) complete according to this Form 8-K?

AbbVie completed the acquisition of Apogee Therapeutics, Inc.. Apogee shareholders received $135.11 per share in cash, for a total equity value of approximately $10.9 billion, and Apogee is now part of AbbVie.

How will the Apogee acquisition affect AbbVie (ABBV) earnings per share?

AbbVie expects the acquisition to reduce adjusted diluted EPS by $0.14 in 2026 (partial year) and by approximately $0.46 in 2027, with the transaction becoming accretive to adjusted diluted EPS beginning in 2032.

What EPS guidance does AbbVie (ABBV) reaffirm for full-year 2026?

AbbVie reaffirms 2026 full-year adjusted diluted EPS guidance in the range of $13.87 to $14.07. This range includes a $0.14 per share dilutive impact from the completed Apogee acquisition and a $0.58 per share unfavorable impact from acquired IPR&D and milestones through Q2.

What is AbbVie’s (ABBV) adjusted EPS guidance for third-quarter 2026?

AbbVie reaffirms its third-quarter 2026 adjusted diluted EPS guidance range of $3.84 to $3.88. This guidance excludes any impact from acquired IPR&D and milestones that may be incurred in the quarter.

What are the key pipeline assets AbbVie gains from Apogee Therapeutics?

AbbVie gains zumilokibart (APG777), a late-stage IL‑13 monoclonal antibody for atopic dermatitis, and APG273, a potential best-in-category long-acting combination targeting IL‑13 and TSLP for asthma, plus a broader pipeline for atopic dermatitis, asthma and COPD.

What clinical results has zumilokibart demonstrated so far?

In a Phase 2 trial for atopic dermatitis, approximately two-thirds of patients on zumilokibart achieved significant skin clearance at 16 weeks, with notable itch reduction and overall disease control, supporting quarterly or twice-yearly maintenance dosing and a favorable safety profile.

How significant is AbbVie’s current immunology franchise mentioned in the filing?

AbbVie states that more than 1 million patients worldwide are treated with its immunology medicines, which are approved in more than 175 countries across 19 immune-mediated diseases, underscoring the scale of its existing immunology business.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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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): September 3, 2026

 

ABBVIE INC.

(Exact name of registrant as specified in its charter)

 

Delaware   001-35565   32-0375147
(State or other jurisdiction
of incorporation or organization)
  (Commission File Number)   (I.R.S Employer
Identification Number)

 

 

1 North Waukegan Road

North Chicago, Illinois 60064-6400

(Address of principal executive offices) (Zip Code)

 

Registrant’s telephone number, including area code: (847) 932-7900

 

Former name or former address, if changed since last report: Not Applicable

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation to 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))

 

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 Stock, $0.01 Par Value   ABBV   New York Stock Exchange
        NYSE Texas
0.750% Senior Notes due 2027   ABBV27   New York Stock Exchange
2.125% Senior Notes due 2028   ABBV28   New York Stock Exchange
2.625% Senior Notes due 2028   ABBV28B   New York Stock Exchange
2.125% Senior Notes due 2029   ABBV29   New York Stock Exchange
1.250% Senior Notes due 2031   ABBV31   New York Stock Exchange

 

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. ¨

 

 

 

 

 

Item 7.01Regulation FD Disclosure

 

On September 3, 2026, AbbVie Inc. (the “Company”) issued a press release announcing the completion of its acquisition of Apogee Therapeutics, Inc. The press release is attached hereto as Exhibit 99.1 and incorporated by reference herein.

 

The information in this Item 7.01, including the exhibit referenced herein and attached hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”), nor shall it be deemed incorporated by reference in any Company filing under the Securities Act of 1933 or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.

 

Forward-Looking Statements

 

Some statements in this Current Report on Form 8-K are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words “believe,” “expect,” “anticipate,” “project” and similar expressions and uses of future or conditional verbs generally identify forward-looking statements. Statements in this Current Report on Form 8-K that are forward-looking may include, but are not limited to, statements regarding AbbVie’s 2026 full-year and third-quarter adjusted diluted EPS guidance, the anticipated benefits of AbbVie’s completed acquisition of Apogee and AbbVie’s ability to successfully integrate Apogee’s operations, employees and pipeline; the expected impact of the acquisition on AbbVie’s adjusted diluted earnings per share; and the anticipated development, regulatory progress and commercial potential of Apogee’s pipeline assets. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements. Such risks and uncertainties include, but are not limited to: the amount and timing of acquired IPR&D and milestones expense; the risk that the anticipated benefits and synergies of the Apogee acquisition may not be realized, or may take longer to realize than expected; risks and costs related to integrating Apogee’s business, employees and pipeline into AbbVie, including the possibility that such integration may be more difficult, time-consuming or costly than anticipated; the risk that acquired in-process research and development assets, including zumilokibart (APG777) and APG273, may not demonstrate the anticipated success, safety or efficacy in ongoing or future clinical trials, and that positive interim or earlier-stage results may not be predictive of results in later-stage or larger clinical trials; the risk of unknown or contingent liabilities assumed in connection with the acquisition; challenges to intellectual property; competition from other products; difficulties inherent in the research and development process; adverse litigation or government action; changes to laws and regulations applicable to our industry; the impact of global macroeconomic factors, such as economic downturns or uncertainty, international conflict, trade disputes and tariffs, and other uncertainties and risks associated with global business operations. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie’s operations is set forth in Item 1A, “Risk Factors,” of AbbVie’s 2026 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its Quarterly Reports on Form 10-Q and in other documents that AbbVie subsequently files with the Securities and Exchange Commission that update, supplement or supersede such information. AbbVie undertakes no obligation, and specifically declines, to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.

 

 

 

 

Item 9.01Financial Statements and Exhibits

 

(d) Exhibits. The following exhibits are provided as part of this Form 8-K:

 

Exhibit No.   Description
99.1   Press Release, dated September 3, 2026, issued by AbbVie Inc.
104   Cover Page Interactive Data File (formatted as Inline XBRL).

 

 

 

 

SIGNATURES

 

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

 

  ABBVIE INC.
   
Date: September 3, 2026
   
  By: /s/ Scott T. Reents
    Scott T. Reents
    Executive Vice President,
    Chief Financial Officer

 

 

 

 

Exhibit 99.1

 

 

AbbVie Completes Acquisition of Apogee Therapeutics

 

Acquisition deepens AbbVie's robust immunology pipeline with diverse assets targeting dermatologic, respiratory and other inflammatory and immunological diseases
Apogee's lead asset, zumilokibart, is a late-stage, half-life extended monoclonal antibody targeting IL-13, in development for patients with atopic dermatitis
Apogee's pipeline also includes APG273, a potential best-in-category long-acting combination targeting IL-13 and thymic stromal lymphopoietin (TSLP), in development for asthma
AbbVie reaffirms previously issued 2026 full-year adjusted diluted EPS guidance range of $13.87 - $14.07; reaffirms previously issued third-quarter adjusted diluted EPS guidance range of $3.84 - $3.88

 

NORTH CHICAGO, Ill., Sept. 3, 2026 – AbbVie (NYSE: ABBV) today announced that it has completed its acquisition of Apogee Therapeutics, Inc. (NASDAQ: APGE). With completion of the acquisition, Apogee is now part of AbbVie. Under the terms of the agreement, Apogee shareholders received $135.11 per share in cash, for a total equity value of approximately $10.9 billion.

 

"The completion of the Apogee acquisition is an important step in further strengthening AbbVie's leadership in immunology and advancing our long-term growth strategy," said Robert A. Michael, chairman and chief executive officer, AbbVie. "By combining Apogee's innovative science with AbbVie's proven development, regulatory and commercial capabilities, we aim to accelerate these programs and bring promising new treatment options to patients living with serious inflammatory and immunological diseases. We are excited to welcome the talented Apogee team to AbbVie and build on their important work."

 

Apogee's pipeline includes novel antibodies targeting multiple validated inflammatory pathways in large immunology and inflammation markets, including atopic dermatitis (AD), asthma, and chronic obstructive pulmonary disease (COPD).

 

AbbVie Inc. +1 (847) 938-9190
1 North Waukegan Road abbvie.com
North Chicago, IL 60064  

 

 

 

 

 

 

Zumilokibart targets IL-13, a critical cytokine in type 2 inflammation, and a central driver of inflammatory diseases like AD and asthma. Specifically in AD, a majority of patients do not achieve simultaneous itch and skin improvement which represents an opportunity for the development of novel treatments that not only provide better skin clearance and itch resolution but also improve convenience with less frequent dosing. In its Phase 2 clinical trial, zumilokibart attained clinically significant results, with approximately two-thirds of patients on treatment achieving significant skin clearance at 16 weeks, along with notable improvements in itch reduction and overall disease control. These findings support its potential best-in-category profile, including strong efficacy and convenient dosing, in patients with AD. Longer-term data from the same trial also support maintenance regimens of either quarterly or twice a year dosing. The safety profile of zumilokibart is favorable and consistent with other medicines in its class, and the molecule has the potential to be evaluated in several additional inflammatory indications.

 

Beyond zumilokibart, Apogee has built a broader pipeline of novel antibodies targeting multiple validated inflammatory pathways. APG273 combines zumilokibart with APG333, an antibody that blocks thymic stromal lymphopoietin (TSLP), a signaling protein that acts as an early trigger of inflammation in the lungs. Phase 1 data showed that APG333 has a long half-life and was able to suppress relevant type 2 inflammatory markers for up to six months after dosing. The Phase 1 data with APG333 and positive interim results from a Phase 1b study of zumilokibart in asthma, support the potential of the APG273 combination with quarterly or twice-yearly injections in asthma.

 

For additional background on the acquisition, please read the announcement press release here and view AbbVie's investor presentation here.

 

Financial Terms

 

AbbVie has acquired all outstanding Apogee common stock for $135.11 per share in cash, for a total equity value of approximately $10.9 billion. Apogee's common stock ceased trading on the NASDAQ stock exchange prior to market open on Sept. 3, 2026. AbbVie expects its acquisition of Apogee to negatively impact adjusted diluted earnings per share (EPS) by $0.14 in 2026 (partial year) and approximately $0.46 in 2027, with accretion beginning in 2032.

 

Full-year 2026 Outlook

 

AbbVie is reaffirming its previously issued 2026 full-year adjusted diluted EPS guidance range of $13.87 - $14.07. This guidance includes a $0.14 per share dilutive impact related to the completed Apogee acquisition. AbbVie's 2026 adjusted diluted EPS guidance includes an unfavorable impact of $0.58 per share related to acquired IPR&D and milestones expense incurred year-to-date through the second quarter. The company's 2026 adjusted diluted EPS guidance excludes any impact from acquired IPR&D and milestones that may be incurred beyond the second quarter of 2026, as both cannot be reliably forecasted.

 

AbbVie is reaffirming its previously issued 2026 third-quarter adjusted diluted EPS guidance range of $3.84 - $3.88. AbbVie's 2026 third-quarter adjusted diluted EPS guidance excludes any impact from acquired IPR&D and milestones that may be incurred in the quarter, as both cannot be reliably forecasted.

 

AbbVie Inc. +1 (847) 938-9190
1 North Waukegan Road abbvie.com
North Chicago, IL 60064  

 

 

 

 

 

 

About AbbVie in Immunology

 

AbbVie is relentless in our pursuit to redefine the standard of care for patients living with immune-mediated conditions, with the goal of helping them live a life free from the limitations of their disease. For more than 20 years, AbbVie has led and helped shape the field of immunology through groundbreaking science and trusted medicines. Building on deep expertise across gastroenterology, rheumatology and dermatology, and other areas of high unmet need, we continue to invest in a broad and differentiated pipeline – spanning innovative modalities, novel mechanisms of action and next-generation approaches designed to conquer the complex biology underlying immune-mediated disease.

 

Today, more than 1 million patients worldwide are treated with AbbVie's immunology medicines, approved in more than 175 countries across 19 immune-mediated diseases that impact adult and pediatric populations. As we work to strengthen our legacy and drive the next wave of innovation, we remain focused on delivering meaningful progress for patients and expanding access to our medicines. For more information, please visit www.abbvie.com/immunology.

 

About AbbVie

 

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, neuroscience and oncology – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

 

Forward-Looking Statements

 

Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions and uses of future or conditional verbs generally identify forward-looking statements. Statements in this news release that are forward-looking may include, but are not limited to, statements regarding AbbVie’s 2026 full-year and third-quarter adjusted diluted EPS guidance, the anticipated benefits of AbbVie's completed acquisition of Apogee and AbbVie's ability to successfully integrate Apogee's operations, employees and pipeline; the expected impact of the acquisition on AbbVie's adjusted diluted earnings per share; and the anticipated development, regulatory progress and commercial potential of Apogee's pipeline assets. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements. Such risks and uncertainties include, but are not limited to: the amount and timing of acquired IPR&D and milestones expense; the risk that the anticipated benefits and synergies of the Apogee acquisition may not be realized, or may take longer to realize than expected; risks and costs related to integrating Apogee's business, employees and pipeline into AbbVie, including the possibility that such integration may be more difficult, time-consuming or costly than anticipated; the risk that acquired in-process research and development assets, including zumilokibart (APG777) and APG273, may not demonstrate the anticipated success, safety or efficacy in ongoing or future clinical trials, and that positive interim or earlier-stage results may not be predictive of results in later-stage or larger clinical trials; the risk of unknown or contingent liabilities assumed in connection with the acquisition; challenges to intellectual property; competition from other products; difficulties inherent in the research and development process; adverse litigation or government action; changes to laws and regulations applicable to our industry; the impact of global macroeconomic factors, such as economic downturns or uncertainty, international conflict, trade disputes and tariffs, and other uncertainties and risks associated with global business operations. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2026 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its Quarterly Reports on Form 10-Q and in other documents that AbbVie subsequently files with the Securities and Exchange Commission that update, supplement or supersede such information. AbbVie undertakes no obligation, and specifically declines, to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.

 

###

 

Media:   Investors:
Catherine Langel Liz Shea
catherine.langel@abbvie.com liz.shea@abbvie.com

 

AbbVie Inc. +1 (847) 938-9190
1 North Waukegan Road abbvie.com
North Chicago, IL 60064  

 

 

 

Filing Exhibits & Attachments

5 documents