Financial Release
- Reports Third-Quarter Diluted EPS of
$1.00 on a GAAP Basis, a Decrease of 54.8 Percent; Adjusted Diluted EPS of$2.95 , a Decrease of 19.4 Percent; These Results Include an Unfavorable Impact of$0.04 Per Share Related to Acquired IPR&D and Milestones Expense
- Delivers Third-Quarter Net Revenues of
$13.927 Billion , a Decrease of 6.0 Percent on a Reported Basis and 5.8 Percent on an Operational Basis
- Third-Quarter Global Net Revenues from the Immunology Portfolio Were
$6.783 Billion , a Decrease of 11.3 Percent; Global Humira Net Revenues Were$3.547 Billion ; Global Skyrizi Net Revenues Were$2.126 Billion ; Global Rinvoq Net Revenues Were$1.110 Billion
- Third-Quarter Global Net Revenues from the Oncology Portfolio Were
$1.512 Billion a Decrease of 8.4 Percent on a Reported Basis, or 8.6 Percent on an Operational Basis; Global Imbruvica Net Revenues Were$908 Million ; Global Venclexta Net Revenues Were$590 Million
- Third-Quarter Global Net Revenues from the Neuroscience Portfolio Were
$2.043 Billion , an Increase of 22.1 Percent on a Reported Basis, or 22.0 Percent on an Operational Basis; Global Botox Therapeutic Net Revenues Were$748 Million ; Global Vraylar Net Revenues Were$751 Million ; Combined Global Ubrelvy and Qulipta Net Revenues Were$365 Million
- Third-Quarter Global Net Revenues from the Aesthetics Portfolio Were
$1.239 Billion , a Decrease of 4.7 Percent on a Reported Basis, or 4.0 Percent on an Operational Basis; Global Botox Cosmetic Net Revenues Were$620 Million ; Global Juvederm Net Revenues Were$321 Million
- Raises 2023
Adjusted Diluted EPS Guidance Range from$10.86 -$11.06 to$11.19 -$11.23 , which Includes an Unfavorable Impact of$0.27 Per Share Related to Acquired IPR&D and Milestones Expense Incurred Year-To-Date Through the Third Quarter 2023
- Raises 2024 Adjusted Diluted EPS Guidance Floor from
$10.70 to$11.00 , which Excludes any Impact Related to Acquired IPR&D and Milestones Expense
- Announces 2024 Dividend Increase of 4.7 Percent, Beginning with Dividend Payable in
February 2024
NORTH CHICAGO, Ill.,
"We delivered another quarter of outstanding results driven by accelerating performance across our non-Humira growth platform, which is demonstrating double-digit growth," said
Third-Quarter Results
- Worldwide net revenues were
$13.927 billion , a decrease of 6.0 percent on a reported basis, or 5.8 percent on an operational basis.
- Global net revenues from the immunology portfolio were
$6.783 billion , a decrease of 11.3 percent.- Global Humira net revenues of
$3.547 billion decreased 36.2 percent.U.S. Humira net revenues were$3.020 billion , a decrease of 39.1 percent. Internationally, Humira net revenues were$527 million , a decrease of 12.6 percent on a reported basis, or 12.2 percent on an operational basis. - Global Skyrizi net revenues were
$2.126 billion , an increase of 52.1 percent on a reported basis, or 51.9 percent on an operational basis. - Global Rinvoq net revenues were
$1.110 billion , an increase of 59.8 percent on a reported basis, or 59.6 percent on an operational basis.
- Global Humira net revenues of
- Global net revenues from the oncology portfolio were
$1.512 billion , a decrease of 8.4 percent on a reported basis, or 8.6 percent on an operational basis.- Global Imbruvica net revenues were
$908 million , a decrease of 20.0 percent, withU.S. net revenues of$678 million and international profit sharing of$230 million . - Global Venclexta net revenues were
$590 million , an increase of 14.6 percent on a reported basis, or 14.0 percent on an operational basis.
- Global Imbruvica net revenues were
- Global net revenues from the neuroscience portfolio were
$2.043 billion , an increase of 22.1 percent on a reported basis, or 22.0 percent on an operational basis.- Global Botox Therapeutic net revenues were
$748 million , an increase of 7.1 percent on a reported basis, or 7.4 percent on an operational basis. - Global Vraylar net revenues were
$751 million , an increase of 35.4 percent. - Global Ubrelvy net revenues were
$233 million , an increase of 45.6 percent. - Global Qulipta net revenues were
$132 million .
- Global Botox Therapeutic net revenues were
- Global net revenues from the aesthetics portfolio were
$1.239 billion , a decrease of 4.7 percent on a reported basis, or 4.0 percent on an operational basis.- Global Botox Cosmetic net revenues were
$620 million , a decrease of 2.7 percent on a reported basis, or 1.7 percent on an operational basis. - Global Juvederm net revenues were
$321 million , a decrease of 8.6 percent on a reported basis, or 7.9 percent on an operational basis.
- Global Botox Cosmetic net revenues were
- On a GAAP basis, the gross margin ratio in the third quarter was 53.4 percent. The adjusted gross margin ratio was 83.5 percent.
- On a GAAP basis, selling, general and administrative (SG&A) expense was 24.2 percent of net revenues. The adjusted SG&A expense was 23.9 percent of net revenues.
- Research and development (R&D) expense on a GAAP and adjusted basis was 12.4 percent of net revenues, reflecting funding actions supporting all stages of our pipeline.
- Acquired IPR&D and milestones expense was 0.5 percent of net revenues.
- On a GAAP basis, the operating margin in the third quarter was 16.4 percent. The adjusted operating margin was 46.7 percent.
- Net interest expense was
$398 million .
- On a GAAP basis, the tax rate in the quarter was 8.8 percent. The adjusted tax rate was 15.7 percent.
- Diluted EPS in the third quarter was
$1.00 on a GAAP basis. Adjusted diluted EPS, excluding specified items, was$2.95 . These results include an unfavorable impact of$0.04 per share related to acquired IPR&D and milestones expense.
Note: "Operational" comparisons are presented at constant currency rates that reflect comparative local currency net revenues at the prior year's foreign exchange rates. |
Recent Events
- AbbVie announced that it submitted applications for a new indication to the
U.S. Food and Drug Administration (FDA) andEuropean Medicines Agency (EMA) for Skyrizi (risankizumab) for the treatment of adult patients with moderately to severely active ulcerative colitis (UC). The submissions are supported by two Phase 3 clinical trials demonstrating Skyrizi achieved the primary endpoint of clinical remission (per AdaptedMayo Score ) and key secondary endpoints as an induction and maintenance treatment. Skyrizi is part of a collaboration betweenBoehringer Ingelheim and AbbVie, with AbbVie leading development and commercialization globally.
- AbbVie announced positive topline results from SEQUENCE, a Phase 3 study evaluating Skyrizi versus Stelara (ustekinumab) in patients with moderately to severely active Crohn's disease (CD) who have failed one or more anti-TNF therapies. In the study, Skyrizi met both primary endpoints (non-inferiority for clinical remission per CDAI at week 24 and superiority of endoscopic remission at week 48) versus Stelara. All secondary endpoints in the trial achieved statistical significance for superiority versus Stelara. Safety results were consistent with the overall safety profile of Skyrizi, with no new safety risks identified.
- AbbVie announced that its Phase 2b study evaluating Rinvoq (upadacitinib) in adults with non-segmental vitiligo (NSV) met the primary endpoint of percent change from baseline in the Facial Vitiligo Area Scoring Index (F-VASI) at week 24 with the 11 mg and 22 mg doses versus placebo. The percent reduction from baseline in F-VASI at week 52 was numerically greater than results at week 24 for all Rinvoq doses. No new safety signals were identified beyond the known safety profile for Rinvoq. Based on these data, AbbVie is advancing its clinical program of Rinvoq in vitiligo to Phase 3.
- At the United European Gastroenterology (UEG) Week 2023, AbbVie shared 23 abstracts, including 11 oral presentations and 12 poster presentations, spanning research on Skyrizi and Rinvoq in both CD and UC. Highlights included late-breaking data from the head-to-head Phase 3 SEQUENCE study evaluating Skyrizi versus Stelara in CD, primary efficacy and safety results from the Phase 3 INSPIRE induction study for Skyrizi in UC, as well as analyses on clinical and endoscopic outcomes from AbbVie's maintenance trials for Skyrizi and Rinvoq in CD and for Rinvoq in UC.
- At the
European Academy of Dermatology and Venereology (EADV)Congress , AbbVie announced new data analyses from the Measure Up 1, Measure Up 2 and AD Up Phase 3 studies that further demonstrated the long-term efficacy and safety profile of Rinvoq among adults and adolescents 12 years and older with moderate to severe atopic dermatitis (AD). Across all 3 studies, response rates forEASI 75 and vIGA-AD 0/1 (co-primary endpoints) and forEASI 90 and WP-NRS 0/1 at week 16 were sustained through week 140 among patients treated with Rinvoq. Safety results were consistent with the known safety profile of Rinvoq, with no new safety signals observed.
- AbbVie announced that the
European Commission (EC) granted conditional marketing authorization for Tepkinly (epcoritamab) as a monotherapy for the treatment of adult patients with relapsed or refractory (r/r) diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy. Tepkinly is the first and only subcutaneous T-cell engaging bispecific antibody approved for the treatment of this patient population in theEuropean Union (EU). This conditional marketing authorization approval represents AbbVie's second approved hematological cancer treatment in the EU and is supported by data from the pivotal Phase 1/2 EPCORE NHL-1 clinical trial. Tepkinly is being co-developed by AbbVie and Genmab.
- In
August 2023 , as part of Inflation Reduction Act (IRA) of 2022, the company's oncology product Imbruvica, sold in theU.S. , was included on the list of products selected for price negotiation by theCenters for Medicare & Medicaid Services (CMS). The selection contributed to a significant decrease in the estimated future cash flows for the product and represented a triggering event which required the company to evaluate the underlying definite lived-intangible asset for impairment. The company utilized a discounted cash flow analysis to estimate the fair value of the intangible asset resulting in a partial impairment of both the gross and net carrying amount. Based on the revised cash flows, the company recorded a pre-tax impairment charge of$2.1 billion to cost of products sold in the condensed consolidated statement of earnings for the third quarter of 2023. The remaining intangible asset carrying value related to Imbruvica in theU.S. totaled$1.8 billion as ofSeptember 30, 2023 .
- AbbVie announced results from CANOVA, a Phase 3 study evaluating Venclexta (venetoclax) plus dexamethasone (VenDex) for patients with t(11;14)-positive r/r multiple myeloma (MM) who received two or more prior treatments. Data did not demonstrate that the treatment combination significantly improved progression-free survival (PFS), the primary endpoint of the trial. Patients receiving VenDex showed improvement in median PFS of 9.9 months compared to 5.8 months with the combination of study comparator pomalidomide and dexamethasone (PomDex); however, the results did not reach statistical significance. Results were presented at the
International Myeloma Society (IMS) Annual Meeting and AbbVie will discuss the data with health authorities to further understand the potential of venetoclax as a biomarker-driven therapy in MM. Venclexta is being developed by AbbVie and Roche. It is jointly commercialized by AbbVie andGenentech , a member of the Roche Group, in theU.S. and by AbbVie outside of theU.S.
- AbbVie announced that the (EC) approved Aquipta (atogepant) for the prophylaxis of migraine in adults who have four or more migraine days per month. The approval makes Aquipta the only once-daily oral calcitonin gene-related peptide (CGRP) receptor antagonist (gepant) treatment in the EU for the preventive treatment of both chronic and episodic migraine. The approval is based on two pivotal Phase 3 studies that demonstrated statistically significant reduction in mean monthly migraine days with Aquipta compared to placebo in adult patients with both chronic and episodic migraine.
- Allergan Aesthetics announced positive topline results from the second of three Phase 3 clinical studies evaluating Botox Cosmetic (onabotulinumtoxinA) for the treatment of moderate to severe platysma prominence associated with platysma muscle activity. All primary and secondary endpoints were met for this study and results were consistent with findings from the first Phase 3 study. Results support Botox Cosmetic as a potential treatment option for moderate to severe platysma prominence and data will be included as part of an upcoming FDA regulatory submission expected near the end of the year. If approved, Botox Cosmetic will be the first and only neurotoxin for this indication.
- Allergan Aesthetics announced positive topline results from two pivotal Phase 3 clinical studies evaluating trenibotulinumtoxinE (BoNT/E) for the treatment of moderate to severe glabellar lines. All primary and secondary endpoints were met for both studies and results support trenibotulinumtoxinE as a novel botulinum neurotoxin serotype E characterized by a rapid onset of action as early as 8 hours after administration and short duration of effect within 2-3 weeks.
- AbbVie announced that it exercised its exclusive right to acquire of Mitokinin, a discovery-stage biotechnology company developing a potentially first-in-class disease-modifying treatment for Parkinson's Disease (PD). Mitokinin's lead compound, a selective PINK1 activator, is designed to address mitochondrial dysfunction that is believed to be a major contributing factor to PD pathogenesis and progression.
Full-Year 2023 Outlook
AbbVie is raising its adjusted diluted EPS guidance for the full year 2023 from $10.86 -
AbbVie Raises 2024 EPS Guidance Floor
AbbVie is raising its adjusted diluted EPS guidance floor for the full year 2024 from
Company Declares Dividend Increase of 4.7 Percent
AbbVie is announcing today that its board of directors declared an increase in the company's quarterly cash dividend from
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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: immunology, oncology, neuroscience and eye care - and products and services across our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X (formerly Twitter), Facebook, Instagram, YouTube or LinkedIn.
Conference Call
AbbVie will host an investor conference call today at
Non-GAAP Financial Results
Financial results for 2023 and 2022 are presented on both a reported and a non-GAAP basis. Reported results were prepared in accordance with GAAP and include all revenue and expenses recognized during the period. Non-GAAP results adjust for certain non-cash items and for factors that are unusual or unpredictable, and exclude those costs, expenses, and other specified items presented in the reconciliation tables later in this release. AbbVie's management believes non-GAAP financial measures provide useful information to investors regarding AbbVie's results of operations and assist management, analysts, and investors in evaluating the performance of the business. Non-GAAP financial measures should be considered in addition to, and not as a substitute for, measures of financial performance prepared in accordance with GAAP.
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. 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 challenges to intellectual property, competition from other products, difficulties inherent in the research and development process, adverse litigation or government action, and changes to laws and regulations applicable to our industry. 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 2022 Annual Report on Form 10-K, which has been filed with the
Key Product Revenues Quarter Ended (Unaudited) |
|||||||||||||||
% Change vs. 3Q22 |
|||||||||||||||
Net Revenues (in millions) |
Reported |
Operationala |
|||||||||||||
|
Int'l. |
Total |
|
Int'l. |
Total |
Int'l. |
Total |
||||||||
NET REVENUES |
|
|
|
(7.7) % |
0.8 % |
(6.0) % |
1.4 % |
(5.8) % |
|||||||
Immunology |
5,696 |
1,087 |
6,783 |
(14.7) |
12.1 |
(11.3) |
11.9 |
(11.3) |
|||||||
Humira |
3,020 |
527 |
3,547 |
(39.1) |
(12.6) |
(36.2) |
(12.2) |
(36.2) |
|||||||
Skyrizi |
1,875 |
251 |
2,126 |
53.5 |
42.5 |
52.1 |
40.7 |
51.9 |
|||||||
Rinvoq |
801 |
309 |
1,110 |
59.0 |
61.8 |
59.8 |
61.2 |
59.6 |
|||||||
Oncology |
973 |
539 |
1,512 |
(12.3) |
(0.4) |
(8.4) |
(1.0) |
(8.6) |
|||||||
Imbruvicab |
678 |
230 |
908 |
(20.2) |
(19.6) |
(20.0) |
(19.6) |
(20.0) |
|||||||
Venclexta |
281 |
309 |
590 |
8.1 |
21.1 |
14.6 |
19.9 |
14.0 |
|||||||
Epkinlyc |
14 |
— |
14 |
n/m |
n/m |
n/m |
n/m |
n/m |
|||||||
Aesthetics |
759 |
480 |
1,239 |
— |
(11.4) |
(4.7) |
(9.7) |
(4.0) |
|||||||
Botox Cosmetic |
388 |
232 |
620 |
5.0 |
(13.3) |
(2.7) |
(10.9) |
(1.7) |
|||||||
Juvederm Collection |
116 |
205 |
321 |
(6.4) |
(9.8) |
(8.6) |
(8.7) |
(7.9) |
|||||||
Other Aesthetics |
255 |
43 |
298 |
(4.0) |
(8.1) |
(4.6) |
(7.0) |
(4.4) |
|||||||
Neuroscience |
1,817 |
226 |
2,043 |
24.0 |
8.9 |
22.1 |
8.4 |
22.0 |
|||||||
Botox Therapeutic |
626 |
122 |
748 |
7.2 |
6.5 |
7.1 |
8.6 |
7.4 |
|||||||
Vraylar |
750 |
1 |
751 |
35.2 |
>100.0 |
35.4 |
>100.0 |
35.4 |
|||||||
Duodopa |
25 |
93 |
118 |
10.6 |
6.6 |
7.4 |
2.3 |
4.0 |
|||||||
Ubrelvy |
230 |
3 |
233 |
43.7 |
>100.0 |
45.6 |
>100.0 |
45.6 |
|||||||
Qulipta |
131 |
1 |
132 |
>100.0 |
n/m |
>100.0 |
n/m |
>100.0 |
|||||||
Other Neuroscience |
55 |
6 |
61 |
(31.9) |
6.2 |
(29.9) |
9.6 |
(29.7) |
|||||||
|
310 |
295 |
605 |
(14.0) |
13.1 |
(2.7) |
13.9 |
(2.4) |
|||||||
Ozurdex |
34 |
86 |
120 |
(4.5) |
22.3 |
13.2 |
21.7 |
12.8 |
|||||||
Lumigan/Ganfort |
28 |
63 |
91 |
(53.0) |
2.7 |
(24.8) |
1.4 |
(25.5) |
|||||||
Alphagan/Combigan |
30 |
40 |
70 |
(16.0) |
10.1 |
(3.1) |
17.3 |
0.4 |
|||||||
Restasis |
104 |
13 |
117 |
(20.7) |
35.0 |
(17.0) |
42.1 |
(16.5) |
|||||||
Other |
114 |
93 |
207 |
16.3 |
11.9 |
14.2 |
12.0 |
14.2 |
|||||||
Other Key Products |
751 |
212 |
963 |
(4.6) |
4.4 |
(2.8) |
4.9 |
(2.7) |
|||||||
Mavyret |
167 |
203 |
370 |
(12.3) |
5.2 |
(3.5) |
5.8 |
(3.2) |
|||||||
Creon |
305 |
— |
305 |
(9.1) |
n/m |
(9.1) |
n/m |
(9.1) |
|||||||
Linzess/ |
279 |
9 |
288 |
6.8 |
(11.1) |
6.2 |
(13.0) |
6.1 |
a |
"Operational" comparisons are presented at constant currency rates that reflect comparative local currency net revenues at the prior year's foreign exchange rates. |
b |
Reflects profit sharing for Imbruvica international revenues. |
c |
Reflects profit sharing for Epkinly |
n/m = not meaningful |
Key Product Revenues Nine Months Ended (Unaudited) |
|||||||||||||||
% Change vs. 9M22 |
|||||||||||||||
Net Revenues (in millions) |
Reported |
Operationala |
|||||||||||||
|
Int'l. |
Total |
|
Int'l. |
Total |
Int'l. |
Total |
||||||||
NET REVENUES |
|
|
|
(8.2) % |
(1.8) % |
(6.8) % |
1.6 % |
(6.0) % |
|||||||
Immunology |
15,963 |
3,220 |
19,183 |
(10.9) |
4.6 |
(8.6) |
8.1 |
(8.1) |
|||||||
Humira |
9,420 |
1,680 |
11,100 |
(30.8) |
(17.9) |
(29.1) |
(14.8) |
(28.7) |
|||||||
Skyrizi |
4,648 |
721 |
5,369 |
50.9 |
41.8 |
49.6 |
45.5 |
50.1 |
|||||||
Rinvoq |
1,895 |
819 |
2,714 |
54.4 |
56.1 |
54.9 |
61.0 |
56.4 |
|||||||
Oncology |
2,807 |
1,599 |
4,406 |
(15.6) |
(1.3) |
(10.9) |
0.2 |
(10.4) |
|||||||
Imbruvicab |
1,982 |
711 |
2,693 |
(23.4) |
(18.0) |
(22.0) |
(18.0) |
(22.0) |
|||||||
Venclexta |
811 |
888 |
1,699 |
9.4 |
18.1 |
13.8 |
21.4 |
15.5 |
|||||||
Epkinlyc |
14 |
— |
14 |
n/m |
n/m |
n/m |
n/m |
n/m |
|||||||
Aesthetics |
2,365 |
1,558 |
3,923 |
(4.9) |
— |
(3.0) |
5.3 |
(1.0) |
|||||||
Botox Cosmetic |
1,217 |
747 |
1,964 |
(1.1) |
0.7 |
(0.4) |
6.0 |
1.6 |
|||||||
Juvederm Collection |
363 |
681 |
1,044 |
(13.3) |
(0.8) |
(5.6) |
4.5 |
(2.3) |
|||||||
Other Aesthetics |
785 |
130 |
915 |
(6.3) |
0.5 |
(5.4) |
5.4 |
(4.7) |
|||||||
Neuroscience |
4,929 |
694 |
5,623 |
18.0 |
7.9 |
16.7 |
11.7 |
17.2 |
|||||||
Botox Therapeutic |
1,827 |
388 |
2,215 |
11.3 |
10.9 |
11.3 |
16.6 |
12.3 |
|||||||
Vraylar |
1,967 |
3 |
1,970 |
33.6 |
>100.0 |
33.7 |
>100.0 |
33.7 |
|||||||
Duodopa |
74 |
279 |
353 |
2.8 |
— |
0.6 |
1.1 |
1.5 |
|||||||
Ubrelvy |
574 |
7 |
581 |
18.8 |
>100.0 |
20.3 |
>100.0 |
20.3 |
|||||||
Qulipta |
292 |
2 |
294 |
>100.0 |
n/m |
>100.0 |
n/m |
>100.0 |
|||||||
Other Neuroscience |
195 |
15 |
210 |
(51.3) |
6.4 |
(49.3) |
11.8 |
(49.1) |
|||||||
|
938 |
892 |
1,830 |
(25.8) |
5.5 |
(13.3) |
9.0 |
(11.9) |
|||||||
Ozurdex |
107 |
247 |
354 |
2.6 |
13.1 |
9.7 |
16.1 |
11.7 |
|||||||
Lumigan/Ganfort |
142 |
198 |
340 |
(23.6) |
(3.1) |
(12.9) |
(0.9) |
(11.8) |
|||||||
Alphagan/Combigan |
90 |
116 |
206 |
(43.5) |
4.2 |
(24.0) |
10.6 |
(21.4) |
|||||||
Restasis |
265 |
43 |
308 |
(48.8) |
14.2 |
(44.5) |
20.1 |
(44.1) |
|||||||
Other |
334 |
288 |
622 |
13.0 |
5.1 |
9.2 |
8.6 |
10.9 |
|||||||
Other Key Products |
2,222 |
616 |
2,838 |
(1.0) |
(1.2) |
(1.1) |
2.1 |
(0.4) |
|||||||
Mavyret |
531 |
590 |
1,121 |
(5.6) |
(1.5) |
(3.5) |
1.8 |
(1.8) |
|||||||
Creon |
892 |
— |
892 |
(5.2) |
n/m |
(5.2) |
n/m |
(5.2) |
|||||||
Linzess/ |
799 |
26 |
825 |
7.7 |
7.0 |
7.7 |
9.3 |
7.8 |
a |
"Operational" comparisons are presented at constant currency rates that reflect comparative local currency net revenues at the prior year's foreign exchange rates. |
b |
Reflects profit sharing for Imbruvica international revenues. |
c |
Reflects profit sharing for Epkinly |
n/m = not meaningful |
AbbVie Inc. Consolidated Statements of Earnings (Unaudited) |
|||||||
(in millions, except per share data) |
Third Quarter Ended |
Nine Months Ended |
|||||
2023 |
2022 |
2023 |
2022 |
||||
Net revenues |
$ 13,927 |
$ 14,812 |
$ 40,017 |
$ 42,933 |
|||
Cost of products sold |
6,485 |
5,022 |
14,711 |
13,244 |
|||
Selling, general and administrative |
3,372 |
3,304 |
9,679 |
11,843 |
|||
Research and development |
1,723 |
1,614 |
5,748 |
4,720 |
|||
Acquired IPR&D and milestones |
66 |
40 |
496 |
454 |
|||
Other operating expense (income), net |
— |
229 |
(179) |
57 |
|||
Total operating costs and expenses |
11,646 |
10,209 |
30,455 |
30,318 |
|||
Operating earnings |
2,281 |
4,603 |
9,562 |
12,615 |
|||
Interest expense, net |
398 |
497 |
1,306 |
1,568 |
|||
Net foreign exchange loss |
25 |
36 |
97 |
108 |
|||
Other expense (income), net |
(95) |
(330) |
3,121 |
427 |
|||
Earnings before income tax expense |
1,953 |
4,400 |
5,038 |
10,512 |
|||
Income tax expense |
172 |
448 |
989 |
1,139 |
|||
Net earnings |
1,781 |
3,952 |
4,049 |
9,373 |
|||
Net earnings attributable to noncontrolling interest |
3 |
3 |
8 |
10 |
|||
Net earnings attributable to |
$ 1,778 |
$ 3,949 |
$ 4,041 |
$ 9,363 |
|||
Diluted earnings per share attributable to |
$ 1.00 |
$ 2.21 |
$ 2.26 |
$ 5.24 |
|||
Adjusted diluted earnings per sharea |
$ 2.95 |
$ 3.66 |
$ 8.32 |
$ 10.18 |
|||
Weighted-average diluted shares outstanding |
1,771 |
1,776 |
1,772 |
1,777 |
a Refer to the Reconciliation of GAAP Reported to Non-GAAP Adjusted Information for further details. |
AbbVie Inc. Reconciliation of GAAP Reported to Non-GAAP Adjusted Information (Unaudited) |
|||||
1. Specified items impacted results as follows: |
|||||
Quarter Ended |
|||||
(in millions, except per share data) |
Earnings |
Diluted |
|||
Pre-tax |
After-taxa |
EPS |
|||
As reported (GAAP) |
$ 1,953 |
$ 1,778 |
$ 1.00 |
||
Adjusted for specified items: |
|||||
Intangible asset amortization |
2,039 |
1,728 |
0.98 |
||
Intangible asset impairment |
2,114 |
1,660 |
0.93 |
||
Acquisition and integration costs |
60 |
54 |
0.03 |
||
Change in fair value of contingent consideration |
8 |
8 |
— |
||
Other |
59 |
22 |
0.01 |
||
As adjusted (non-GAAP) |
$ 6,233 |
$ 5,250 |
$ 2.95 |
a Represents net earnings attributable to |
|||||||
Intangible asset impairment reflects a partial impairment charge related to the |
|||||||
Reported GAAP earnings and adjusted non-GAAP earnings for the three months ended |
|||||||
2. The impact of the specified items by line item was as follows: |
|||||||
Quarter Ended |
|||||||
(in millions) |
Cost of |
SG&A |
R&D |
Other |
|||
As reported (GAAP) |
$ 6,485 |
$ 3,372 |
$ 1,723 |
$ (95) |
|||
Adjusted for specified items: |
|||||||
Intangible asset amortization |
(2,039) |
— |
— |
— |
|||
Intangible asset impairment |
(2,114) |
— |
— |
— |
|||
Acquisition and integration costs |
(18) |
(40) |
(2) |
— |
|||
Change in fair value of contingent consideration |
— |
— |
— |
(8) |
|||
Other |
(13) |
(2) |
(1) |
(43) |
|||
As adjusted (non-GAAP) |
$ 2,301 |
$ 3,330 |
$ 1,720 |
$ (146) |
3. The adjusted tax rate for the third quarter of 2023 was 15.7 percent, as detailed below: |
|||||
Quarter Ended |
|||||
(dollars in millions) |
Pre-tax |
Income taxes |
Tax rate |
||
As reported (GAAP) |
$ 1,953 |
$ 172 |
8.8 % |
||
Specified items |
4,280 |
808 |
18.9 % |
||
As adjusted (non-GAAP) |
$ 6,233 |
$ 980 |
15.7 % |
Reconciliation of GAAP Reported to Non-GAAP Adjusted Information (Unaudited) |
|||||
1. Specified items impacted results as follows: |
|||||
Quarter Ended |
|||||
(in millions, except per share data) |
Earnings |
Diluted |
|||
Pre-tax |
After-taxa |
EPS |
|||
As reported (GAAP) |
$ 4,400 |
$ 3,949 |
$ 2.21 |
||
Adjusted for specified items: |
|||||
Intangible asset amortization |
2,024 |
1,673 |
0.94 |
||
Intangible asset impairment |
770 |
604 |
0.34 |
||
Acquisition and integration costs |
348 |
348 |
0.20 |
||
Change in fair value of contingent consideration |
(214) |
(218) |
(0.12) |
||
Litigation matters |
110 |
94 |
0.05 |
||
Other |
58 |
78 |
0.04 |
||
As adjusted (non-GAAP) |
$ 7,496 |
$ 6,528 |
$ 3.66 |
a Represents net earnings attributable to |
||||||||||
Acquisition and integration costs primarily reflect integration costs related to the Allergan acquisition. Other primarily |
||||||||||
Reported GAAP earnings and adjusted non-GAAP earnings for the three months ended |
||||||||||
2. The impact of the specified items by line item was as follows: |
||||||||||
Quarter Ended |
||||||||||
(in millions) |
Cost of |
SG&A |
R&D |
Other |
Other |
|||||
As reported (GAAP) |
$ 5,022 |
$ 3,304 |
$ 1,614 |
$ 229 |
$ (330) |
|||||
Adjusted for specified items: |
||||||||||
Intangible asset amortization |
(2,024) |
— |
— |
— |
— |
|||||
Intangible asset impairment |
(770) |
— |
— |
— |
— |
|||||
Acquisition and integration costs |
(22) |
(91) |
(6) |
(229) |
— |
|||||
Change in fair value of contingent consideration |
— |
— |
— |
— |
214 |
|||||
Litigation matters |
— |
(110) |
— |
— |
— |
|||||
Other |
(39) |
(14) |
(1) |
— |
(4) |
|||||
As adjusted (non-GAAP) |
$ 2,167 |
$ 3,089 |
$ 1,607 |
$ — |
$ (120) |
3. The adjusted tax rate for the third quarter of 2022 was 12.9 percent, as detailed below: |
|||||
Quarter Ended |
|||||
(dollars in millions) |
Pre-tax |
Income taxes |
Tax rate |
||
As reported (GAAP) |
$ 4,400 |
$ 448 |
10.2 % |
||
Specified items |
3,096 |
517 |
16.7 % |
||
As adjusted (non-GAAP) |
$ 7,496 |
$ 965 |
12.9 % |
Reconciliation of GAAP Reported to Non-GAAP Adjusted Information (Unaudited) |
|||||
1. Specified items impacted results as follows: |
|||||
Nine Months Ended |
|||||
(in millions, except per share data) |
Earnings |
Diluted |
|||
Pre-tax |
After-taxa |
EPS |
|||
As reported (GAAP) |
$ 5,038 |
$ 4,041 |
$ 2.26 |
||
Adjusted for specified items: |
|||||
Intangible asset amortization |
6,057 |
5,101 |
2.87 |
||
Intangible asset impairment |
2,824 |
2,289 |
1.29 |
||
Acquisition and integration costs |
38 |
15 |
0.01 |
||
Change in fair value of contingent consideration |
3,432 |
3,348 |
1.88 |
||
Other |
75 |
16 |
0.01 |
||
As adjusted (non-GAAP) |
$ 17,464 |
$ 14,810 |
$ 8.32 |
a Represents net earnings attributable to |
|||||||||
Acquisition and integration costs primarily reflect integration costs related to the Allergan acquisition, including a one-time |
|||||||||
Reported GAAP earnings and adjusted non-GAAP earnings for the nine months ended |
|||||||||
2. The impact of the specified items by line item was as follows: |
|||||||||
Nine Months Ended |
|||||||||
(in millions) |
Cost of |
SG&A |
R&D |
Other |
Other |
||||
As reported (GAAP) |
$ 14,711 |
$ 9,679 |
$ 5,748 |
$ (179) |
$ 3,121 |
||||
Adjusted for specified items: |
|||||||||
Intangible asset amortization |
(6,057) |
— |
— |
— |
— |
||||
Intangible asset impairment |
(2,194) |
— |
(630) |
— |
— |
||||
Acquisition and integration costs |
(66) |
(134) |
(7) |
169 |
— |
||||
Change in fair value of contingent consideration |
— |
— |
— |
— |
(3,432) |
||||
Other |
(45) |
(13) |
(4) |
10 |
(23) |
||||
As adjusted (non-GAAP) |
$ 6,349 |
$ 9,532 |
$ 5,107 |
$ — |
$ (334) |
3. The adjusted tax rate for the first nine months of 2023 was 15.2 percent, as detailed below: |
|||||
Nine Months Ended |
|||||
(dollars in millions) |
Pre-tax |
Income taxes |
Tax rate |
||
As reported (GAAP) |
$ 5,038 |
$ 989 |
19.6 % |
||
Specified items |
12,426 |
1,657 |
13.3 % |
||
As adjusted (non-GAAP) |
$ 17,464 |
$ 2,646 |
15.2 % |
Reconciliation of GAAP Reported to Non-GAAP Adjusted Information (Unaudited) |
|||||
1. Specified items impacted results as follows: |
|||||
Nine Months Ended |
|||||
(in millions, except per share data) |
Earnings |
Diluted |
|||
Pre-tax |
After-taxa |
EPS |
|||
As reported (GAAP) |
$ 10,512 |
$ 9,363 |
$ 5.24 |
||
Adjusted for specified items: |
|||||
Intangible asset amortization |
5,728 |
4,794 |
2.69 |
||
Intangible asset impairment |
770 |
604 |
0.34 |
||
Acquisition and integration costs |
595 |
567 |
0.32 |
||
Change in fair value of contingent consideration |
647 |
657 |
0.37 |
||
Pylera divestiture |
(172) |
(126) |
(0.07) |
||
Litigation matters |
2,497 |
2,021 |
1.13 |
||
Other |
281 |
295 |
0.16 |
||
As adjusted (non-GAAP) |
$ 20,858 |
$ 18,175 |
$ 10.18 |
a Represents net earnings attributable to |
|||||||||
Acquisition and integration costs primarily reflect integration costs related to the Allergan acquisition. Litigation matters |
|||||||||
Reported GAAP earnings and adjusted non-GAAP earnings for the nine months ended |
|||||||||
2. The impact of the specified items by line item was as follows: |
|||||||||
Nine Months Ended |
|||||||||
(in millions) |
Cost of |
SG&A |
R&D |
Other |
Other |
||||
As reported (GAAP) |
$ 13,244 |
$ 11,843 |
$ 4,720 |
$ 57 |
$ 427 |
||||
Adjusted for specified items: |
|||||||||
Intangible asset amortization |
(5,728) |
— |
— |
— |
— |
||||
Intangible asset impairment |
(770) |
— |
— |
— |
— |
||||
Acquisition and integration costs |
(84) |
(263) |
(19) |
(229) |
— |
||||
Change in fair value of contingent consideration |
— |
— |
— |
— |
(647) |
||||
Pylera divestiture |
— |
— |
— |
172 |
— |
||||
Litigation matters |
— |
(2,497) |
— |
— |
— |
||||
Other |
(160) |
(107) |
(7) |
— |
(7) |
||||
As adjusted (non-GAAP) |
$ 6,502 |
$ 8,976 |
$ 4,694 |
$ — |
$ (227) |
3. The adjusted tax rate for the first nine months of 2022 was 12.8 percent, as detailed below: |
|||||
Nine Months Ended |
|||||
(dollars in millions) |
Pre-tax |
Income taxes |
Tax rate |
||
As reported (GAAP) |
$ 10,512 |
$ 1,139 |
10.8 % |
||
Specified items |
10,346 |
1,534 |
14.8 % |
||
As adjusted (non-GAAP) |
$ 20,858 |
$ 2,673 |
12.8 % |
View original content:https://www.prnewswire.com/news-releases/abbvie-reports-third-quarter-2023-financial-results-301969530.html
SOURCE AbbVie
Media: Gabby Tarbert, (224) 244-0111; Investors: Liz Shea, (847) 935-2211; Todd Bosse, (847) 936-1182; Jeffrey Byrne, (847) 938-2923