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Consumer Discretionary : Textiles, Apparel & Luxury Goods | Small Cap Value
Company profile

Wolverine World Wide, Inc. is a designer, marketer and licensor of a range of quality casual footwear and apparel, performance outdoor and athletic footwear and apparel, kids' footwear, industrial work boots and apparel, and uniform shoes and boots. The Company operates through two segments: Wolverine Michigan Group and Wolverine Boston Group. Its Wolverine Michigan Group consists of footwear and apparel under brand names Merrell, Cat, Wolverine, Chaco, Hush Puppies, Bates uniform footwear, Harley-Davidson and Hytest safety footwear. Its Wolverine Boston Group consists of Sperry footwear, Saucony footwear and apparel, Keds footwear and the kids' footwear business, which includes the Stride Rite licensed business, as well as kids' footwear offerings from Saucony, Sperry, Keds, Merrell, Hush Puppies and Cat. Its products are marketed in approximately 170 countries, including the United States, Canada, the United Kingdom and certain countries in continental Europe and Asia Pacific.

Closing Price
$15.27
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0.37 (2.48%)
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--
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B/A Size
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Day's High
15.39
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14.83
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(Light)
Volume:
1,096,329

10-day average volume:
1,379,401
1,096,329

AbbVie Presents Data from Extensive Portfolio at the American College of Rheumatology Convergence 2022

3:06 pm ET November 8, 2022 (PR Newswire) Print

-- Thirty-six abstracts underscore AbbVie's commitment to advancing research to help more people living with rheumatic diseases

-- Additional analysis of long-term safety data for RINVOQ(R) (upadacitinib) and SKYRIZI(R) (risankizumab)

AbbVie (NYSE: ABBV) today announced it would present new data across its rheumatology portfolio, including RINVOQ(R) (upadacitinib) for rheumatoid arthritis, psoriatic arthritis and axial spondyloarthritis, and SKYRIZI(R) (risankizumab) for psoriasis and psoriatic arthritis at the American College of Rheumatology's annual meeting (ACR Convergence 2022) taking place November 10-14 in Philadelphia, PA, as well as virtually.

"AbbVie has a rich legacy spanning more than two decades where we have consistently worked to deliver new insights and innovation in rheumatology," said Celine Goldberger, M.D., Ph.D., vice president, head of U.S. medical affairs, AbbVie. "Data being presented at this year's ACR meeting further reflect AbbVie's commitment to advancing our portfolio of medicine to help more people living with chronic and debilitating conditions achieve meaningful disease control."

Data to be presented includes:

-- Data on rates of major adverse cardiovascular events (MACE) and venous thromboembolic events (VTE) in the RA, PsA and AS clinical trial programs of upadacitinib.1

-- Real-world data evaluating the impact of a second-line therapeutic product on disease control in patients living with psoriatic arthritis.2

-- Several poster presentations on data from the KEEPsAKE clinical trials evaluating risankizumab in psoriatic arthritis including long-term data across specific sub-groups, and SELECT clinical trials evaluating upadacitinib in psoriatic arthritis, rheumatoid arthritis and axial spondyloarthritis.3-7

Select AbbVie abstracts presented at ACR 2022 are outlined below.

Abstract Title                                                                     Presentation
                                                                                   Details
                                                                                   All times ET
Rheumatoid Arthritis
Safety and Efficacy of Upadacitinib in Patients with Rheumatoid Arthritis and      Abstract #0294;
Inadequate Response or Intolerance to Biologic DMARDs: Results Through 5           Poster Session A;
Years From the SELECT-BEYOND Study                                                 Nov. 12, 2022
                                                                                   1:00-3:00 p.m.
Safety and Efficacy of Upadacitinib in Patients with Rheumatoid Arthritis and      Abstract #0295;
Inadequate Response to Conventional Synthetic DMARDs: Results Through 5            Poster Session A;
Years From the SELECT-NEXT Study                                                   Nov. 12, 2022
                                                                                   1:00-3:00 p.m.
Healthcare Resource Utilization and Economic Burden of Patients with Adequate      Abstract #2006;
and Inadequate Responses to Advanced Therapies for Rheumatoid Arthritis in         Poster Session D;
Japan                                                                              Nov. 14, 2022
                                                                                   1:00-3:00 p.m.
Psoriatic Arthritis
Risankizumab (RZB) Demonstrates Long-Term Efficacy Across Subgroups in             Abstract #0308;
Patients with Active Psoriatic Arthritis (PsA): A Post Hoc, Integrated Analysis    Poster Session A;
From the Phase 3 (KEEPsAKE 1 and KEEPsAKE 2) Studies                               Nov. 12, 2022
                                                                                   1:00-3:00 p.m.
Efficacy of Risankizumab in the Treatment of PsA Patients with Limited and         Abstract #1504;
Extensive Joint Involvement                                                        Poster Session C;
                                                                                   Nov. 13, 2022
                                                                                   1:00-3:00 p.m.
The Impact of Second-Line Therapeutic on Disease Control After Discontinuation     Abstract #1600;
of First Line TNF Inhibitor in Patients with PsA: Analysis from the CorEvitas      Oral Presentation;
Psoriatic Arthritis/Spondylarthritis Registry                                      Room 201;
                                                                                   Nov. 13, 2022
                                                                                   3:45-3:55 p.m.
Axial Spondyloarthritis
Efficacy of Upadacitinib in Patients with Non-Radiographic Axial Spondyloarthritis Abstract #0419;
Stratified by Objective Signs of Inflammation at Baseline                          Poster Session A;
                                                                                   Nov. 13, 2022
                                                                                   1:00-3:00 p.m.
The Impact of Cycling Among Tumor Necrosis Factor Inhibitors on Disease            Abstract #1499;
Control in Patients with Axial Spondyloarthritis: A Study from the CorEvitas       Poster Session C;
PsA/SpA Registry                                                                   Nov. 13, 2022
                                                                                   1:00-3:00 p.m.;
                                                                                   and Live Ignite
                                                                                   Talk at the Center
                                                                                   City Stage, from
                                                                                   1:20-1:25 p.m.
Cross-Rheumatology
Malignancy in the Upadacitinib Clinical Trial Programs for Rheumatoid Arthritis,   Abstract #0292;
Psoriatic Arthritis, and Ankylosing Spondylitis                                    Poster Session A;
                                                                                   Nov. 12, 2022
                                                                                   1:00-3:00 p.m.;
                                                                                   and Live Ignite
                                                                                   Talk at the Center
                                                                                   City Stage on Nov.
                                                                                   14, 2022 1:30-
                                                                                   1:35 p.m.
MACE and VTE Across Upadacitinib Clinical Trial Programs in Rheumatoid             Abstract #0510;
Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis                         Oral Presentation;
                                                                                   Room 119;
                                                                                   Nov. 12, 2022
                                                                                   4:00-4:10 p.m.

SKYRIZI (risankizumab) is part of a collaboration between Boehringer Ingelheim and AbbVie, with AbbVie leading development and commercialization of SKYRIZI globally.

The full list of all 36 abstracts and ACR Convergence 2022 scientific program can be found here.

About RINVOQ(R) (upadacitinib) in the United States

Discovered and developed by AbbVie scientists, RINVOQ is a selective JAK inhibitor that is being studied in several immune-mediated inflammatory diseases. Based on enzymatic and cellular assays, RINVOQ demonstrated greater inhibitory potency for JAK-1 vs JAK-2, JAK-3, and TYK-2.8 The relevance of inhibition of specific JAK enzymes to therapeutic effectiveness and safety is not currently known.

In the U.S., RINVOQ 15 mg is approved for adults with moderately to severely active rheumatoid arthritis who have had an inadequate response or intolerance to one or more TNF blockers; adults with active psoriatic arthritis who have had an inadequate response or intolerance to one or more TNF blockers; adults with active ankylosing spondylitis (AS) who have had an inadequate response or intolerance to one or more tumor necrosis factor (TNF) blockers and adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation who have had an inadequate response or intolerance to TNF blocker therapy.8 RINVOQ 45 mg is approved for use in adult patients with moderately to severely active ulcerative colitis who have had an inadequate response or intolerance to one or more TNF blockers as an induction therapy once daily for 8 weeks. The recommended dose of RINVOQ for maintenance treatment is 15 mg once daily. A dosage of 30 mg once daily may be considered for patients with refractory, severe or extensive disease. Discontinue RINVOQ if an adequate response is not achieved with the 30 mg dose. Use the lowest effective dosage needed to maintain response. RINVOQ 15 mg once daily can also be initiated in adults and children 12 years of age and older weighing at least 40 kg with refractory, moderate to severe atopic dermatitis whose disease is not adequately controlled with other systemic drug products, including biologics or when use of those therapies is inadvisable. In these children and adults less than 65 years of age who do not achieve an adequate response, the dose may be increased to 30 mg once daily.

Phase 3 trials of RINVOQ in rheumatoid arthritis, atopic dermatitis, psoriatic arthritis, axial spondyloarthritis, Crohn's disease, ulcerative colitis, giant cell arteritis and Takayasu arteritis are ongoing.9-16

RINVOQ(R) (upadacitinib) U.S. Use and Important Safety Information8

USESRINVOQ is a prescription medicine used to treat:

-- Adults with moderate to severe rheumatoid arthritis (RA) when 1 or more medicines called tumor necrosis factor (TNF) blockers have been used, and did not work well or could not be tolerated.

-- Adults with active psoriatic arthritis (PsA) when 1 or more medicines called TNF blockers have been used, and did not work well or could not be tolerated.

-- Adults with moderate to severe ulcerative colitis (UC) when 1 or more medicines called TNF blockers have been used, and did not work well or could not be tolerated.

-- Adults with active ankylosing spondylitis (AS) when 1 or more medicines called TNF blockers have been used, and did not work well or could not be tolerated.

-- Adults with active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation when a TNF blocker medicine has been used, and did not work well or could not be tolerated.

It is not known if RINVOQ is safe and effective in children with juvenile idiopathic arthritis, psoriatic arthritis, ulcerative colitis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.

-- Adults and children 12 years of age and older with moderate to severe eczema (atopic dermatitis [AD]) that did not respond to previous treatment and their eczema is not well controlled with other pills or injections, including biologic medicines, or the use of other pills or injections is not recommended.

RINVOQ is safe and effective in children 12 years of age and older weighing at least 88 pounds (40 kg) with atopic dermatitis.

It is not known if RINVOQ is safe and effective in children under 12 years of age with atopic dermatitis.

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about RINVOQ?

RINVOQ may cause serious side effects, including:

-- Serious infections. RINVOQ can lower your ability to fight infections. Serious infections have happened while taking RINVOQ, including tuberculosis (TB) and infections caused by bacteria, fungi, or viruses that can spread throughout the body. Some people have died from these infections. Your healthcare provider (HCP) should test you for TB before starting RINVOQ and check you closely for signs and symptoms of TB during treatment with RINVOQ. You should not start taking RINVOQ if you have any kind of infection unless your HCP tells you it is okay. If you get a serious infection, your HCP may stop your treatment until your infection is controlled. You may be at higher risk of developing shingles (herpes zoster).

-- Increased risk of death in people 50 years and older who have at least 1 heart disease (cardiovascular) risk factor.

-- Cancer and immune system problems. RINVOQ may increase your risk of certain cancers. Lymphoma and other cancers, including skin cancers, can happen. Current or past smokers are at higher risk of certain cancers, including lymphoma and lung cancer. Follow your HCP's advice about having your skin checked for skin cancer during treatment with RINVOQ. Limit the amount of time you spend in sunlight. Wear protective clothing when you are in the sun and use sunscreen.

-- Increased risk of major cardiovascular (CV) events, such as heart attack, stroke, or death, in people 50 years and older who have at least 1 heart disease (CV) risk factor, especially if you are a current or past smoker.

-- Blood clots. Blood clots in the veins of the legs or lungs and arteries can happen with RINVOQ. This may be life-threatening and cause death. Blood clots in the veins of the legs and lungs have happened more often in people who are 50 years and older and with at least 1 heart disease (CV) risk factor.

-- Allergic reactions. Symptoms such as rash (hives), trouble breathing, feeling faint or dizzy, or swelling of your lips, tongue, or throat, that may mean you are having an allergic reaction have been seen in people taking RINVOQ. Some of these reactions were serious. If any of these symptoms occur during treatment with RINVOQ, stop taking RINVOQ and get emergency medical help right away.

-- Tears in the stomach or intestines and changes in certain laboratory tests. Your HCP should do blood tests before you start taking RINVOQ and while you take it. Your HCP may stop your RINVOQ treatment for a period of time if needed because of changes in these blood test results.

Do not take RINVOQ if you are allergic to upadacitinib or any of the ingredients in RINVOQ. See the Medication Guide or Consumer Brief Summary for a complete list of ingredients.

What should I tell my HCP BEFORE starting RINVOQ?

Tell your HCP if you:

-- Are being treated for an infection, have an infection that won't go away or keeps coming back, or have symptoms of an infection, such as:

-- Fever, sweating, or chills

-- Shortness of breath

-- Warm, red, or painful skin or sores on your body

-- Muscle aches

-- Feeling tired

-- Blood in phlegm

-- Diarrhea or stomach pain

-- Cough

-- Weight loss

-- Burning when urinating or urinating more often than normal

-- Have TB or have been in close contact with someone with TB.

-- Are a current or past smoker.

-- Have had a heart attack, other heart problems, or stroke.

-- Have or have had any type of cancer, hepatitis B or C, shingles (herpes zoster), blood clots in the veins of your legs or lungs, diverticulitis (inflammation in parts of the large intestine), or ulcers in your stomach or intestines.

-- Have other medical conditions, including liver problems, low blood cell counts, diabetes, chronic lung disease, HIV, or a weak immune system.

-- Live, have lived, or have traveled to parts of the country, such as the Ohio and Mississippi River valleys and the Southwest, that increase your risk of getting certain kinds of fungal infections. If you are unsure if you've been to these types of areas, ask your HCP.

-- Have recently received or are scheduled to receive a vaccine. People who take RINVOQ should not receive live vaccines.

-- Are pregnant or plan to become pregnant. Based on animal studies, RINVOQ may harm your unborn baby. Your HCP will check whether or not you are pregnant before you start RINVOQ. You should use effective birth control (contraception) to avoid becoming pregnant during treatment with RINVOQ and for 4 weeks after your last dose.

-- Are breastfeeding or plan to breastfeed. RINVOQ may pass into your breast milk. Do not breastfeed during treatment with RINVOQ and for 6 days after your last dose.

Tell your HCP about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. RINVOQ and other medicines may affect each other, causing side effects.

Especially tell your HCP if you take:

-- Medicines for fungal or bacterial infections

-- Rifampicin or phenytoin

-- Medicines that affect your immune system

If you are not sure if you are taking any of these medicines, ask your HCP or pharmacist.

What should I avoid while taking RINVOQ?

Avoid food or drink containing grapefruit during treatment with RINVOQ as it may increase the risk of side effects.

What should I do or tell my HCP AFTER starting RINVOQ?

-- Tell your HCP right away if you have any symptoms of an infection. RINVOQ can make you more likely to get infections or make any infections you have worse.

-- Get emergency help right away if you have any symptoms of a heart attack or stroke while taking RINVOQ, including:

-- Discomfort in the center of your chest that lasts for more than a few minutes or that goes away and comes back

-- Severe tightness, pain, pressure, or heaviness in your chest, throat, neck, or jaw

-- Pain or discomfort in your arms, back, neck, jaw, or stomach

-- Shortness of breath with or without chest discomfort

-- Breaking out in a cold sweat

-- Nausea or vomiting

-- Feeling lightheaded

-- Weakness in one part or on one side of your body

-- Slurred speech

-- Tell your HCP right away if you have any signs or symptoms of blood clots during treatment with RINVOQ, including:

-- Swelling

-- Pain or tenderness in one or both legs

-- Sudden unexplained chest or upper back pain

-- Shortness of breath or difficulty breathing

-- Tell your HCP right away if you have a fever or stomach-area pain that does not go away, and a change in your bowel habits.

What are other possible side effects of RINVOQ?Common side effects include upper respiratory tract infections (common cold, sinus infections), shingles (herpes zoster), herpes simplex virus infections (including cold sores), bronchitis, nausea, cough, fever, acne, headache, increased blood levels of creatine phosphokinase, allergic reactions, inflammation of hair follicles, stomach-area (abdominal) pain, increased weight, flu, tiredness, lower number of certain types of white blood cells (neutropenia, lymphopenia), muscle pain, flu-like illness, rash, increased blood cholesterol levels, and increased liver enzyme levels.

A separation or tear to the lining of the back part of the eye (retinal detachment) has happened in people with atopic dermatitis treated with RINVOQ. Call your HCP right away if you have any sudden changes in your vision during treatment with RINVOQ.

These are not all the possible side effects of RINVOQ.

How should I take RINVOQ?RINVOQ is taken once a day with or without food. Do not split, crush, or chew the tablet. Take RINVOQ exactly as your HCP tells you to use it. RINVOQ is available in 15 mg, 30 mg, and 45 mg extended-release tablets.

This is the most important information to know about RINVOQ. For more information, talk to your HCP.

You are encouraged to report negative side effects of prescription drugs to the FDA.

Visit http://www.fda.gov/medwatch or call 1-800-FDA-1088.

If you are having difficulty paying for your medicine, AbbVie may be able to help. Visit AbbVie.com/myAbbVieAssist to learn more.

Please click here for the Full Prescribing Information and Medication Guide.

Globally, prescribing information varies; refer to the individual country product label for complete information.

About SKYRIZI(R) (risankizumab-rzaa) in the United States17

SKYRIZI is a prescription medicine used to treat adults with moderate to severe plaque psoriasis who may benefit from taking injections or pills (systemic therapy) or treatment using ultraviolet or UV light (phototherapy).

SKYRIZI U.S. Uses and Important Safety Information17

SKYRIZI is a prescription medicine used to treat adults with:

-- moderate to severe plaque psoriasis who may benefit from taking injections or pills (systemic therapy) or treatment using ultraviolet or UV light (phototherapy).

-- active psoriatic arthritis (PsA).

-- moderate to severe Crohn's disease.

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about SKYRIZI(R) (risankizumab-rzaa)?

SKYRIZI is a prescription medicine that may cause serious side effects, including:

Serious allergic reactions:

-- Stop using SKYRIZI and get emergency medical help right away if you get any of the following symptoms of a serious allergic reaction:

-- fainting, dizziness, feeling lightheaded (low blood pressure)

-- swelling of your face, eyelids, lips, mouth, tongue, or throat

-- trouble breathing or throat tightness

-- chest tightness

-- skin rash, hives

-- itching

Infections:SKYRIZI may lower the ability of your immune system to fight infections and may increase your risk of infections. Your healthcare provider should check you for infections and tuberculosis (TB) before starting treatment with SKYRIZI and may treat you for TB before you begin treatment with SKYRIZI if you have a history of TB or have active TB. Your healthcare provider should watch you closely for signs and symptoms of TB during and after treatment with SKYRIZI.

-- Tell your healthcare provider right away if you have an infection or have symptoms of an infection, including:

-- fever, sweats, or chills

-- cough

-- shortness of breath

-- blood in your mucus (phlegm)

-- muscle aches

-- warm, red, or painful skin or sores on your body different from your psoriasis

-- weight loss

-- diarrhea or stomach pain

-- burning when you urinate or urinating more often than normal

Do not use SKYRIZI if you are allergic to risankizumab-rzaa or any of the ingredients in SKYRIZI. See the Medication Guide or Consumer Brief Summary for a complete list of ingredients.

Before using SKYRIZI, tell your healthcare provider about all of your medical conditions, including if you:

-- have any of the conditions or symptoms listed in the section "What is the most important information I should know about SKYRIZI?"

-- have an infection that does not go away or that keeps coming back.

-- have TB or have been in close contact with someone with TB.

-- have recently received or are scheduled to receive an immunization (vaccine). Medicines that interact with the immune system may increase your risk of getting an infection after receiving live vaccines. You should avoid receiving live vaccines right before, during, or right after treatment with SKYRIZI. Tell your healthcare provider that you are taking SKYRIZI before receiving a vaccine.

-- are pregnant or plan to become pregnant. It is not known if SKYRIZI can harm your unborn baby.

-- are breastfeeding or plan to breastfeed. It is not known if SKYRIZI passes into your breast milk.

-- become pregnant while taking SKYRIZI. You are encouraged to enroll in the Pregnancy Registry, which is used to collect information about the health of you and your baby. Talk to your healthcare provider or call 1-877-302-2161 to enroll in this registry.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

What are the possible side effects of SKYRIZI?SKYRIZI may cause serious side effects. See "What is the most important information I should know about SKYRIZI?"

Liver problems in Crohn's disease: A person with Crohn's disease who received SKYRIZI through a vein in the arm developed changes in liver blood tests with a rash that led to hospitalization. Your healthcare provider will do blood tests to check your liver before, during, and up to 12 weeks of treatment and may stop treatment with SKYRIZI if you develop liver problems. Tell your healthcare provider right away if you notice any of the following symptoms: unexplained rash, nausea, vomiting, stomach (abdominal) pain, tiredness (fatigue), loss of appetite, yellowing of the skin and eyes (jaundice), and dark urine.

The most common side effects of SKYRIZI in people treated for Crohn's disease include: upper respiratory infections, headache, joint pain, stomach (abdominal) pain, injection site reactions, low red blood cells (anemia), fever, back pain, and urinary tract infection.

The most common side effects of SKYRIZI in people treated for plaque psoriasis and psoriatic arthritis include: upper respiratory infections, headache, feeling tired, injection site reactions, and fungal skin infections.

These are not all the possible side effects of SKYRIZI. Call your doctor for medical advice about side effects.

Use SKYRIZI exactly as your healthcare provider tells you to use it.

SKYRIZI is available in a 150 mg/mL prefilled syringe and pen, a 600 mg/10 mL vial for intravenous infusion, and a 180 mg/1.2 mL or 360 mg/2.4 mL single-dose prefilled cartridge with on-body injector.

This is the most important information to know about SKYRIZI. For more information, talk to your HCP.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit http://www.fda.gov/medwatch or call 1-800-FDA-1088.

If you are having difficulty paying for your medicine, AbbVie may be able to help. Visit AbbVie.com/myAbbVieAssist to learn more.

Please click here for Full Prescribing Information and Medication Guide for SKYRIZI.

Globally, prescribing information varies; refer to the individual country product label for complete information.

About AbbVie in RheumatologyFor more than 20 years, AbbVie has been dedicated to improving care for people living with rheumatic diseases. Anchored by a longstanding commitment to discovering and delivering transformative therapies, we pursue cutting-edge science that improves our understanding of promising new pathways and targets, ultimately helping more people living with rheumatic diseases reach their treatment goals. For more information, visit AbbVie in rheumatology.

About AbbVieAbbVie'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, eye care, virology, and women's health, in addition to products and services across our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, LinkedIn or Instagram.

Forward-Looking StatementsSome 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, among others, 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 indicated in the forward-looking statements. Such risks and uncertainties include, but are not limited to, failure to realize the expected benefits from AbbVie's acquisition of Allergan plc ("Allergan"), failure to promptly and effectively integrate Allergan's businesses, competition from other products, challenges to intellectual property, difficulties inherent in the research and development process, adverse litigation or government action, changes to laws and regulations applicable to our industry and the impact of public health outbreaks, epidemics or pandemics, such as COVID-19. 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 2021 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its subsequent Quarterly Reports on Form 10-Q. AbbVie undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.

US-MULT-221303

References:

-- Charles-Schoeman C, Choy E, McInnes I, Mysler E, Nash P, Yamaoka K, Lippe R, Khan N, Shmagel A, Palac H, Suboticki J, Curtis J. MACE and VTE Across Upadacitinib Clinical Trial Programs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/mace-and-vte-across-upadacitinib-clinical-trial-programs-in-rheumatoid-arthritis-psoriatic-arthritis-and-ankylosing-spondylitis/. Accessed November 8, 2022.

-- Ogdie A, McLean R, Blachley T, Middaugh N, Mittal M, Clewell J, Ciecinski S, Mease P. The Impact of Second-Line Therapeutic on Disease Control After Discontinuation of First Line TNF Inhibitor in Patients with PsA: Analysis from the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstracts/the-impact-of-second-line-therapeutic-on-disease-control-after-discontinuation-of-first-line-tnf-inhibitor-in-patients-with-psa-analysis-from-the-corevitas-psoriatic-arthritis-spondyloarthritis-regis/. Accessed November 8, 2022.

-- Kwatra S, Khattri S, Amin A, Photowala H, Liu R, Padilla B, Kaplan B, McGonagle D. Impact of Risankizumab on Enthesitis and Dactylitis: Integrated Analysis of the Phase 3, Randomized, Double-Blind KEEPsAKE 1 and 2 Trials [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/impact-of-risankizumab-on-enthesitis-and-dactylitis-integrated-analysis-of-the-phase-3-randomized-double-blind-keepsake-1-and-2-trials/. Accessed November 8, 2022.

-- Erik L, Papp K, White D, Asnal C, Lu W, Soliman A, Padilla B, Chen M, Ostor A. Efficacy and Safety of Risankizumab for Active Psoriatic Arthritis: 100-Week Results from the KEEPsAKE 1 and KEEPsAKE 2 Trials [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/efficacy-and-safety-of-risankizumab-for-active-psoriatic-arthritis-100-week-results-from-the-keepsake-1-and-keepsake-2-trials/. Accessed November 8, 2022.

-- Merola J, Callis-Duffin K, Padilla B, Yue C, Photowala H, Kaplan B, McInnes I. Risankizumab (RZB) Demonstrates Long-Term Efficacy Across Subgroups in Patients with Active Psoriatic Arthritis (PsA): A Post Hoc, Integrated Analysis from the Phase 3 (KEEPsAKE 1 and KEEPsAKE 2) Studies [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/risankizumab-rzb-demonstrates-long-term-efficacy-across-subgroups-in-patients-with-active-psoriatic-arthritis-psa-a-post-hoc-integrated-analysis-from-the-phase-3-keepsake-1-and-keepsake-2-stud/. Accessed November 8, 2022.

-- Merola J, McInnes I, Kavanaugh A, Nash P, Xue Z, Stakias V, Eldred A, Ciecinski S, Douglas K, Coates L. Effects of Treatment with Risankizumab on Minimal Disease Activity and Disease Activity in Psoriatic Arthritis: An Analysis of the KEEPsAKE-1 and -2 Trials [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/effects-of-treatment-with-risankizumab-on-minimal-disease-activity-and-disease-activity-in-psoriatic-arthritis-an-analysis-of-the-keepsake-1-and-2-trials/. Accessed November 8, 2022.

-- Ogdie A, Merola J, Ranza R, Soliman A, Mittal M, Padilla B, Ciecinski S, Nakasato P, Gossec L. Association Between Stringent Clinical Measures of Disease Activity and Clinically Meaningful Improvements in Patient-Reported Outcomes in Psoriatic Arthritis: Results from KEEPsAKE 1 and 2 Clinical Trials [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/association-between-stringent-clinical-measures-of-disease-activity-and-clinically-meaningful-improvements-in-patient-reported-outcomes-in-psoriatic-arthritis-results-from-keepsake-1-and-2-clinical-t/. Accessed November 8, 2022.

-- RINVOQ(R) (upadacitinib) [Package Insert]. North Chicago, Ill.: AbbVie Inc.

-- A study comparing upadacitinib (ABT-494) to placebo and to adalimumab in adults with rheumatoid arthritis who are on a stable dose of methotrexate and who have an inadequate response to methotrexate (SELECT-COMPARE). ClinicalTrials.gov identifier: NCT02629159. Accessed November 8, 2022. https://www.clinicaltrials.gov/ct2/show/NCT02629159

-- A Study to Evaluate the Safety and Efficacy of ABT-494 for Induction and Maintenance Therapy in Subjects With Moderately to Severely Active Ulcerative Colitis. ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT02819635. Accessed on November 8, 2022.

-- A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of ABT-494 for the Induction of Symptomatic and Endoscopic Remission in Subjects With Moderately to Severely Active Crohn's Disease Who Have Inadequately Responded to or Are Intolerant to Immunomodulators or Anti-TNF Therapy. ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT02365649. Accessed on November 8, 2022.

-- A Study to Evaluate the Safety and Efficacy of Upadacitinib in Participants With Giant Cell Arteritis (SELECT-GCA). ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT03725202. Accessed on November 8, 2022.

-- A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Participants With Psoriatic Arthritis Who Have an Inadequate Response to at Least One Non-Biologic Disease Modifying Anti-Rheumatic Drug (SELECT - PsA 1). ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT03104400. Accessed on November 8, 2022.

-- A Study to Compare Safety and Efficacy of Upadacitinib to Dupilumab in Adult Participants With Moderate to Severe Atopic Dermatitis (Heads Up). ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT03738397. Accessed on November 8, 2022.

-- Study to Evaluate the Efficacy and Safety of Upadacitinib in Subjects With Takayasu Arteritis (SELECT-TAK). ClinicalTrials.gov. Available at https://clinicaltrials.gov/ct2/show/record/NCT04161898. Accessed on November 8, 2022.

-- A Study to Evaluate Efficacy and Safety of Upadacitinib in Adult Participants With Axial Spondyloarthritis (SELECT AXIS 2). ClinicalTrials.gov. Available at: https://clinicaltrials.gov/ct2/show/NCT04169373. Accessed on November 8, 2022.

-- SKYRIZI(R) (risankizumab) [Package Insert]. North Chicago, Ill.: AbbVie Inc.

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