56%
SKYRIZI
Percentage of patients
Learn how AbbVie could help you save. 1.866.SKYRIZI
In a study of 352 patients comparing SKYRIZI to Otezla
56%
SKYRIZI
Percentage of patients
5%
Otezla
Percentage of patients
This 1-year (52-week) study compared SKYRIZI to Otezla for the treatment of adults with moderate plaque psoriasis who qualify for oral medications or biologics. It was a 2-part study set up to evaluate the effectiveness of SKYRIZI and Otezla at 16 weeks and 1 year. Overall safety was observed throughout the study.
Patients were aware of the treatments they were taking, which may have influenced results.
OTEZLA® is a registered trademark of Amgen Inc.
In a study of 393 patients comparing SKYRIZI to Sotyktu
57%
SKYRIZI
Percentage of patients
23%
Sotyktu
Percentage of patients
This 1-year (52-week) study compared SKYRIZI to Sotyktu for the treatment of adults with moderate plaque psoriasis who have not taken a biologic before and qualify for oral medications or biologics. It was a 2-part study set up to evaluate the effectiveness of SKYRIZI and Sotyktu at 16 weeks and 1 year. Overall safety was observed throughout the study.
Patients were aware of the treatments they were taking, which may have influenced results.
SOTYKTU® is a registered trademark of Bristol-Myers Squibb Company.
In 2 separate studies, patients were given a treatment satisfaction questionnaire with a total of 9 questions across 3 categories. In Study 1 of SKYRIZI and Otezla with 110 participants, those on SKYRIZI responded to a treatment satisfaction questionnaire about SKYRIZI. In Study 2 of SKYRIZI and Sotyktu with 127 participants, those on SKYRIZI responded to a treatment satisfaction questionnaire about SKYRIZI. Ask your dermatologist about the treatment satisfaction questionnaire.
Average patient-reported treatment satisfaction scores for SKYRIZI at Week 16*
In these studies, patients were aware of the treatments they were taking, which may have influenced results. TSQM-9 data were not completed by all patients in the studies. Data presented here were the data available at 16 weeks.
*Scores are based on the 9-item Treatment Satisfaction Questionnaire (TSQM-9).
OTEZLA® is a registered trademark of Amgen Inc.
SOTYKTU® is a registered trademark of Bristol-Myers Squibb Company.
Most common side effects at 16 weeks in this study
Most common side effects through 1 year were consistent with those at 16 weeks and also included nasopharyngitis (inflammation of the nasal passages and the throat) and upper respiratory tract infections for SKYRIZI and nasopharyngitis for Otezla.
OTEZLA® is a registered trademark of Amgen Inc.
Most common side effects at 16 weeks in this study
Side effects will be assessed throughout this 1-year study.
SOTYKTU® is a registered trademark of Bristol-Myers Squibb Company.
These 2 separate studies were not designed to make conclusions about safety. These are not all the possible side effects of SKYRIZI, Otezla, or Sotyktu. How frequently these side effects occur may change with longer treatment. Refer to the medication guide of each product to talk to your doctor about the benefits and risks of these medications. See Important Safety Information for more about the safety of SKYRIZI.
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 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.
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.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
SKYRIZI may cause serious side effects. See "What is the most important information I should know about SKYRIZI?"
Liver problems may happen while being treated for Crohn's disease or ulcerative colitis: 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 at least 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 and ulcerative colitis include: upper respiratory infections, headache, joint pain, stomach (abdominal) pain, injection site reactions, low red blood cells (anemia), fever, back pain, urinary tract infection, and rash.
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 (risankizumab-rzaa) 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.
SKYRIZI is a prescription medicine used to treat adults with:
US-SKZ-240065
Please see the Full Prescribing Information, including the Medication Guide, for SKYRIZI.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit 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/PatientAccessSupport to learn more.
Legal Notices. © 2024 AbbVie. All rights reserved. If you have any questions about AbbVie’s SKYRIZI.com website that have not been answered, click here. This website and the information contained herein is intended for use by US residents only, is provided for informational purposes only and is not intended to replace a discussion with a healthcare provider. All decisions regarding patient care must be made with a healthcare provider and consider the unique characteristics of each patient.