Ixekizumab is a subcutaneously administered humanized IgG4 monoclonal antibody that selectively binds to the interleukin-17A (IL-17A) cytokine, inhibiting its interaction with the IL-17A receptor. Interleukin-17A is involved in normal inflammatory and immune responses. Elevated concentrations of IL-17A are found in several inflammatory conditions, and thus ixekizumab is helpful in treating many such conditions. The drug is approved for use in adult and pediatric patients 6 years and older with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy and is also used in adults for psoriatic arthritis (PsA), for ankylosing spondylitis (AS), and for non-radiographic axial spondyloarthritis. Treatment of plaque psoriasis with ixekizumab results in significant improvement in psoriatic skin lesions and a reduction of itching and inflammation. The drug is also effective in treating active psoriatic arthritis (PsA), by improving physical function, pain, swelling, and inhibiting the progression of structural joint damage. It may be used as monotherapy or in combination with a conventional disease-modifying antirheumatic drug (cDMARD) (e.g., methotrexate). For adults with ankylosing spondylitis, ixekizumab improves clinical signs and symptoms of active disease, which can improve quality of life; cDMARDs and other conventional, non-biologic treatments and analgesics may be continued during use. In treating non-radiographic axial spondyloarthritis in adults, a higher percentage of patients with non-radiographic axial spondyloarthritis achieved an Assessment of Spondyloarthritis International Society 40 (ASAS40) response after 52 weeks of therapy with ixekizumab compared to placebo; as with other indications, cDMARDs and other conventional, non-biologic treatments may be continued during use. The ideal therapy for individual patients with plaque psoriasis, PsA, or AS is determined by treat to target strategies, severity of disease, and response or contraindications to treatments. While TNF-blockers are often first-line biologic treatments, IL-17 inhibitors, the IL-inhibiting biologics, may be considered when the patient has severe disease and either has contraindications/adverse reactions to TNF-blocking biologics or inadequate response. As with other interleukin inhibitors, ixekizumab may increase the risk of infection.
General Administration Information
For storage information, see the specific product information within the How Supplied section.
Route-Specific Administration
Injectable Administration
-Administer by subcutaneous injection only.
-Visually inspect parenteral products for particulate matter and discoloration prior to administration whenever solution and container permit. The solution should be free of visible particles, clear, and colorless to slightly yellow.
Subcutaneous Administration
-Ixekizumab is available as a prefilled syringe and as an autoinjector. Each device contains 80 mg ixekizumab.
-The product is intended for use under the guidance and supervision of a physician
--Adults may self-inject or caregivers may give subcutaneous injections after proper training.
-Caregivers may give injections of the 80 mg dose to pediatric patients weighing more than 50 kg using the autoinjector or prefilled syringe after training and demonstration of proper subcutaneous injection technique.
-Pediatric doses of 20 mg or 40 mg must be prepared and administered by a qualified healthcare professional.
-Each 160 mg dose is administered as 2 subcutaneous injections of 80 mg.
-Administration sites for patient administration include upper arms, thighs, and any quadrant of the abdomen. Healthcare professionals may inject in the upper, outer arm.
-Do not administer where the skin is tender, bruised, erythematous, indurated or affected by psoriasis.
-Rotate sites of injection with each dose. Injections should be administered at a different location than was used for the previous injection.
-Wash hands with soap and water before drug administration. Clean injection site with an alcohol wipe and let dry.
-Ixekizumab does not contain preservatives; therefore, discard any unused product remaining in the prefilled syringe or autoinjector. Discard the single-dose autoinjector or syringe after use in a proper puncture-resistant container.
-Missed doses: If a dose or administration time is missed, administer the missed dose as soon as possible. Thereafter, resume dosing at the regularly scheduled time.
Preparation for the use of the 80 mg/mL prefilled syringe or autoinjector:
-Remove prefilled syringe or autoinjector from the refrigerator and allow 30 minutes to reach room temperature. DO NOT use any methods to speed the warming process, such as a microwave, hot water, or sunlight.
-Inspect syringe or autoinjector for particulate matter and discoloration prior to administration. The autoinjector contains glass parts; do not use the autoinjector if it is dropped on a hard surface.
-Storage of unopened prefilled-syringes and autoinjectors: Protect from light and store refrigerated at 2 to 8 degrees C (36 to 46 degrees F) until time of use. Do not freeze and do not use the injection if it has been frozen. Do not shake.-If needed, a prefilled-syringe or autoinjector may be stored at room temperature up to 30 degrees C (86 degrees F) for up to 5 days in the original carton to protect from light. Once the product has been stored at room temperature, do not return to the refrigerator and discard, if unused, within 5 days.
-Record the date when first removed from the refrigerator in the spaces provided on the carton.
-For the 2 or 3 autoinjector pack, remove a single autoinjector at the time, leaving the remaining autoinjector(s) in the original carton in the refrigerator. Ensure the unrefrigerated autoinjector is protected from light.
Preparation of the 20 mg and 40 mg pediatric doses using the 80 mg/mL prefilled syringe:
-Must be prepared and administered by a qualified healthcare professional.
-Gather the following supplies:
--0.5 mL or 1 mL disposable syringe
-sterile needle for withdrawal
-27-gauge sterile needle for administration
-sterile, clear glass vial
-Expel the entire contents of the prefilled syringe into the sterile vial. DO NOT shake or swirl the vial. DO NOT add any other medication to the vial.
-Using the 0.5 mL or 1 mL disposable syringe and sterile needle, withdraw the prescribed dose from the vial (i.e., 0.25 mL for 20 mg dose; 0.5 mL for 40 mg dose).
-Remove the needle from the syringe and replace it with a 27-gauge needle prior to administration to the patient.
-Storage of prepared 20 mg or 40 mg pediatric dose: If necessary, the prepared dose may be stored at room temperature for up to 4 hours from first puncturing the sterile vial.
Autoinjector:
-If you have vision or hearing problems, do not use autoinjector without help from a caregiver.
-Make sure the lock ring is in the lock position, and leave the base cap on until you are ready to inject. Do not touch the needle.
-Twist off the base cap in the direction of the arrows and throw it in the trash. Do not put the cap back on once it has been removed from the autoinjector.
-Place the clear base flat and firmly against your skin at the injection site. Turn the lock ring to the unlock position.
-Press the green injection button. There will be a loud click. Keep holding the clear base firmly against your skin. You will hear a 2nd click in about 10 seconds to indicate the injection is complete. You will see the gray plunger at the top of the clear base.
-Remove the autoinjector from your skin.
Prefilled syringe:
-If you have vision problems, do not use the prefilled syringe without help from a caregiver.
-Pull the needle cap off and throw it away. Do not put the cap back on once it has been removed from the autoinjector. Do not touch the needle.
-Gently pinch and hold a fold of skin where you will inject.
-Insert the needle at a 45-degree angle. Then let go of your skin before you push the plunger. Make sure to keep the needle in place.
-Slowly push the thumb pad to push the plunger all the way in until all the medicine is injected. You should see the green plunger rod show through the syringe body when the injection is complete.
-Remove the needle from the skin.
Hypersensitivity reactions can occur with the administration of ixekizumab. During clinical trials, angioedema and urticaria developed in less than 0.1% and in up to 1.7% of patients treated with ixekizumab, respectively. In addition, anaphylaxis, including cases resulting in hospitalization, has been reported during postmarketing use. If anaphylactoid reactions or other serious hypersensitivity reaction occurs, institute appropriate therapy and immediately discontinue ixekizumab. Patients should not inject additional doses if a serious hypersensitivity reaction occurs.
During clinical trials, an injection site reaction was reported in 17% of those receiving ixekizumab and 3% of those receiving placebo. Most reactions consisted of erythema and/or pain at the site, and were mild-to-moderate in severity; most reactions did not result in treatment discontinuation.
During the entire treatment period used in clinical trials (60 weeks), neutropenia occurred in 11% of subjects administered ixekizumab compared to 3% of those receiving placebo. The incidence was lower during weeks 13 to 60 than during weeks 0 to 12. During the 12 week period, neutropenia Grade 3 (less than 1,000 cells/mm3) or more was reported in 0.2% of those receiving ixekizumab compared to 0.1% of those receiving placebo. The majority of cases were either Grade 2 (2% vs. 0.3% placebo; 1,000 to less than 1,500 cells/mm3) or Grade 1 (7% vs. 3% placebo; 1,500 to less than 2,000 cells/mm3). Neutropenia was not associated with an increased rate of infection in the ixekizumab group compared to placebo. Thrombocytopenia also was reported during ixecuzumab clinical trials (incidence not reported). The vast majority (98%) of cases were Grade 1 (3% vs. 1% placebo; 75,000 to less than 150,000 cells/mm3). Thrombocytopenia was not associated with an increased rate of bleeding in those receiving ixekizumab compared to placebo.
Ixekizumab administration may increase the risk of infection. During placebo-controlled clinical trials, infections were reported in 27% of patients treated with ixekizumab compared to 23% of those receiving placebo. Upper respiratory tract infections (includes naso-pharyngitis and rhinovirus infection) were reported in 14% of those receiving ixekizumab compared to 13% in the placebo group. Other infectious diseases reported more frequently in the ixekizumab group compared to placebo during clinical trials include oral candidiasis (less than 1%), influenza (up to 1.7% for plaque psoriasis; 1.3% for psoriatic arthritis), tinea infections (2% vs. less than 1%), and conjunctivitis (ocular infection; up to 2.6% for plaque psoriasis; 1.3% for psoriatic arthritis). Rhinitis also was reported in clinical trials (less than 1%). Patients should be instructed to seek medical advice if signs or symptoms of infection develop. If a patient develops a serious infection, discontinue ixekizumab until the infection resolves.
Gastrointestinal adverse events have been reported with the use of ixekizumab. Nausea was reported in 2% of patients. During adult clinical trials, Crohn's disease and ulcerative colitis, including exacerbations of inflammatory bowel disease, were reported in 0.1% to 1% and 0.2% to 0.5% of patients, respectively. In a 12-week pediatric plaque psoriasis trial, Crohn's disease occurred in 0.9% of drug recipients.
The development of immunogenicity (antibody formation) may occur with the use of ixekizumab. During the 60-week treatment period for adult plaque psoriasis, approximately 22% of patients had developed antibodies to ixekizumab; approximately 10% of those who developed antibodies to ixekizumab had antibodies classified as neutralizing, which are associated with reduced drug concentration and loss of efficacy. In a 12-week pediatric plaque psoriasis trial, 18% of drug recipients developed anti-drug antibodies; 4% had confirmed neutralizing antibodies associated with low drug concentrations. During the 52-week clinical trial for psoriatic arthritis, 11% developed ixekizumab antibodies, the majority of which were low titer, and 8% had confirmed neutralizing antibodies. Among patients with ankylosing spondylitis who were treated for up to 16 weeks, 5.2% developed ixekizumab antibodies and 1.5% of these patients were found to have neutralizing antibodies. In the 52-week, non-radiographic axial spondyloarthritis clinical trial, 8.9% of patients treated with ixekizumab developed anti-drug antibodies; no patient developed neutralizing antibodies. The clinical effect of antibodies to ixekizumab is dependent on antibody titer, and higher antibody titers were associated with decreasing drug concentration and clinical response. The assay used to detect ixekizumab antibodies has limitations in detecting neutralizing antibodies in the presence of ixekizumab; therefore, the incidence of antibody development may not have been reliably determined. Furthermore, the detection of antibodies is dependent on the sensitivity and specificity of the assay, and the incidence of positive antibodies may be influenced by assay methodology, sample handling, the timing of sample collection, concomitant medications, and underlying disease. Therefore, the incidence of antibody formation to ixekizumab cannot be directly compared to other products.
Ixekizumab is contraindicated in patients with a previous serious hypersensitivity reaction, such as anaphylaxis, to ixekizumab or to any of the product excipients. Ixekizumab is associated with a risk of serious hypersensitivity reactions or anaphylaxis; angioedema and urticaria occurred in the ixekizumab group in clinical trials. In addition, anaphylaxis, including cases resulting in hospitalization, has been reported during postmarketing use. If an anaphylactic or other clinically significant hypersensitivity reaction occurs, institute appropriate therapy and immediately discontinue ixekizumab. Patients should not inject additional doses if a serious hypersensitivity reaction occurs.
Ixekizumab may increase the risk of infection and may increase the risk for reactivation of latent infections, due to its effects on the immune system. Do not initiate ixekizumab until any clinically important active infection in a patient resolves or is adequately treated. Instruct patients treated with ixekizumab to seek medical advice if signs or symptoms of clinically important chronic or acute infection occur. If a patient develops a serious infection or is not responding to standard therapy, monitor the patient closely and discontinue ixekizumab until the infection resolves. In clinical trials, a higher rate of infections was reported with ixekizumab compared to placebo. Serious bacterial infection, fungal infection and viral infection may occur. Patients with a chronic infection or a history of recurrent infections or with underlying conditions that may predispose them to infections (e.g., patients with immunosuppression), or those who have lived in certain infection endemic areas may not be appropriate candidates for ixekizumab therapy. Carefully consider the benefits and risks of therapy before drug initiation.
Evaluate all patients for tuberculosis before ixekizumab initiation. Ixekizumab should not be administered to patients with active tuberculosis infection. Treatment of latent tuberculosis should be initiated prior to treatment with ixekizumab. Consider antituberculosis therapy before ixekizumab receipt in patients with a history of latent or active tuberculosis without a confirmed adequate treatment course. Monitor patients closely for signs and symptoms of active tuberculosis infection during and after treatment with ixekizumab. Patients who have lived in tuberculosis endemic areas may not be appropriate candidates for ixekizumab therapy. Carefully consider the benefits and risks of therapy before drug initiation.
Use ixekizumab cautiously in patients with inflammatory bowel disease including Crohn's disease and ulcerative colitis. During ixekizumab clinical trials, cases of Crohn's disease and inflammatory bowel disease, including exacerbations, were reported. Monitor patients closely for signs and symptoms of onset or exacerbation of inflammatory bowel disease during ixekizumab treatment.
Avoid vaccination of ixekizumab recipients with live virus vaccines. Complete all age appropriate immunizations as recommended by current immunization guidelines prior to initiating ixekizumab therapy. In addition, no data are available on the response to live or inactive vaccines.
Available data regarding the use of ixekizumab during pregnancy are insufficient to evaluate for a drug-associated risk of major birth defects, miscarriages, or other adverse maternal or fetal outcomes. Human IgG does cross the placental barrier; therefore, ixekizumab may be transmitted from mother to fetus. No effects on neonatal development were observed when monkeys were given ixekizumab at dose exposures up to 19-times the maximum recommended human dose (MRHD). When dosing was continued until parturition, neonatal deaths, attributed to early delivery, trauma, or congenital defect, were observed at 1.9-times the MRHD. The clinical significance of these findings is unknown. There is a pregnancy exposure registry that monitors outcomes in pregnant patients exposed to ixekizumab; pregnant patients are encouraged to enroll themselves by calling 1-800-284-1695.
There are no available data on the presence of ixekizumab in human milk, the effects on breast-fed infants, or the effects on milk production. Ixekizumab was detected in the milk of lactating cynomolgus monkeys. When a drug is present in animal milk, it is likely that it will also be present in human milk. Consider the benefits of breast-feeding along with the mother's clinical need for ixekizumab and any potential adverse effects on the breast-fed infant from ixekizumab or the underlying maternal condition. If a breast-feeding infant experiences an adverse effect related to a maternally administered drug, health care providers are encouraged to report the adverse effect to the FDA.
Ixekizumab is approved for the treatment of plaque psoriasis in children 6 years and older. The safety and efficacy of ixekizumab for other pediatric indications (i.e., psoriatic arthritis, ankylosing spondylitis, or non-radiographic sponyloarthritis) and for pediatric patients younger than 6 years of age (i.e., neonates, infants, and young children) have not been established.
Before starting ixekizumab, test potential drug recipients for hepatitis B (surface antigen and core antibody), hepatitis C (IgG), and HIV serum status (HIV-1 and HIV-2 antibodies and HIV-1 antigen). Consider ongoing screening (e.g., annually) in people who are at increased risk for HIV, hepatitis B, or hepatitis C infection. Retest for HIV infection in any person who displays symptoms or other conditions that may suggest HIV seroconversion or infection. In patients found to be infected with HIV, consider involving relevant specialists to ensure HIV viral load is suppressed on antiretroviral therapy. Similarily, retest for viral hepatitis in any person who develops unexplained elevations in hepatic enzymes. It is recommended to consult a hepatologist when using a biological therapy in patients who are infected with hepatitis B or C, whether newly diagnosed or chronically infected.
Patients who undergo surgery while taking a biologic therapy, such as ixekizumab, may be at greater risk for postoperative infections. In patients undergoing elective surgery, balance the risk of postoperative infection against the risk of developing a severe or unstable disease by stopping the biologic therapy. When possible, it is advised to stop the biologic therapy 3- to 5-times the half-live or the length of the treatment cycle (whichever is longer) between the last dose and the planned surgery. Restart the biologic therapy postoperatively if there is no evidence of infection and wound healing is satisfactory.
For the treatment of moderate to severe plaque psoriasis in persons who are candidates for systemic therapy or phototherapy:
Subcutaneous dosage:
Adults: 160 mg subcutaneously at week 0, then 80 mg subcutaneously at weeks 2, 4, 6, 8, 10, and 12, and then 80 mg subcutaneously every 4 weeks. May increase the maintenance dose to 80 mg subcutaneously every 2 weeks if an inadequate primary response may be due to insufficient drug exposure (e.g., known subtherapeutic drug concentrations, obesity, relapse during treatment); however, consider the increased risk for infection and adverse reactions.
Children and Adolescents 6 to 17 years weighing more than 50 kg: 160 mg subcutaneously at week 0, then 80 mg subcutaneously every 4 weeks.
Children and Adolescents 6 to 17 years weighing 25 to 50 kg: 80 mg subcutaneously at week 0, then 40 mg subcutaneously every 4 weeks.
Children and Adolescents 6 to 17 years weighing less than 25 kg: 40 mg subcutaneously at week 0, then 20 mg subcutaneously every 4 weeks.
For the treatment of active psoriatic arthritis, including with coexistent moderate to severe plaque psoriasis:
-for the treatment of active psoriatic arthritis without coexistent moderate to severe plaque psoriasis:
Subcutaneous dosage:
Adults: 160 mg subcutaneously at week 0, then 80 mg subcutaneously every 4 weeks. May be administered alone or in combination with a conventional disease-modifying antirheumatic drug (DMARD).
-for the treatment of active psoriatic arthritis with coexistent moderate to severe plaque psoriasis:
Subcutaneous dosage:
Adults: 160 mg subcutaneously at week 0, then 80 mg subcutaneously at weeks 2, 4, 6, 8, 10, and 12, and then 80 mg subcutaneously every 4 weeks. May be administered alone or in combination with a conventional disease-modifying antirheumatic drug (DMARD).
For the treatment of active ankylosing spondylitis:
Subcutaneous dosage:
Adults: 160 mg subcutaneously at week 0 (administered as two 80-mg injections) followed by 80 mg subcutaneously every 4 weeks. May be administered with conventional disease modifying antirheumatic drugs (DMARDs), corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), or analgesics.
For the treatment of active, non-radiographic axial spondyloarthritis with objective signs of inflammation:
Subcutaneous dosage:
Adults: 80 mg subcutaneously every 4 weeks. May be administered with conventional disease modifying antirheumatic drugs (DMARDs), corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), or analgesics.
Maximum Dosage Limits:
-Adults
160 mg/dose subcutaneously initially, then 80 mg/dose subcutaneously for maintenance therapy for psoriasis, psoriatic arthritis, and ankylosing spondyloarthritis; for non-radiographic axial spondyloarthritis 80 mg/dose subcutaneously.
-Geriatric
160 mg/dose subcutaneously initially, then 80 mg/dose subcutaneously for maintenance therapy for psoriasis, psoriatic arthritis, and ankylosing spondyloarthritis; for non-radiographic axial spondyloarthritis 80 mg/dose subcutaneously.
-Adolescents
more than 50 kg: 160 mg/dose subcutaneously initially, then 80 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
25 to 50 kg: 80 mg/dose subcutaneously initially, then 40 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
less than 25 kg: 40 mg/dose subcutaneously initially, then 20 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
-Children
6 years or older and more than 50 kg: 160 mg/dose subcutaneously initially, then 80 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
6 years or older and 25 to 50 kg: 80 mg/dose subcutaneously initially, then 40 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
6 years or older and less than 25 kg: 40 mg/dose subcutaneously initially, then 20 mg/dose subcutaneously for maintenance therapy of plaque psoriasis; safety and efficacy have not been established for psoriatic arthritis, ankylosing spondylitis, or non-radiographic axial spondyloarthritis.
1 to 5 years: Safety and efficacy have not been established.
-Infants
Not indicated.
-Neonates
Not indicated.
Patients with Hepatic Impairment Dosing
Specific guidelines for dosage adjustments in hepatic impairment are not available; it appears no dosage adjustments are needed.
Patients with Renal Impairment Dosing
Specific guidelines for dosage adjustments in renal impairment are not available; it appears no dosage adjustments are needed.
*non-FDA-approved indication
Abatacept: (Major) Concomitant use of abatacept with other biologic agents, such as ixekizumab, is not recommended because of the possibility of additive immunosuppression and increased risk of infection. There is insufficient experience to assess the safety and efficacy of abatacept administered concurrently with ixekizumab.
Bacillus Calmette-Guerin Vaccine, BCG: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Canakinumab: (Major) Avoid the concomitant use of canakinumab with other interleukin inhibitors, such as ixekizumab; coadministration has not been studied and may result in additive immunosuppression and increased risk of infection.
Chikungunya Vaccine, Live: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Cholera Vaccine: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the live cholera vaccine. When feasible, administer indicated vaccines prior to initiating immunosuppressant medications. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure to cholera bacteria after receiving the vaccine.
Dengue Tetravalent Vaccine, Live: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the dengue virus vaccine. When feasible, administer indicated vaccines at least 2 weeks prior to initiating immunosuppressant medications. If vaccine administration is necessary, consider revaccination following restoration of immune competence. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure after receiving the vaccine.
Intranasal Influenza Vaccine: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Live Vaccines: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Measles Virus; Mumps Virus; Rubella Virus; Varicella Virus Vaccine, Live: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Measles/Mumps/Rubella Vaccines, MMR: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Rotavirus Vaccine: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
SARS-CoV-2 (COVID-19) vaccines: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the SARS-CoV-2 virus vaccine. When feasible, administer indicated vaccines prior to initiating immunosuppressant medications. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure to SARS-CoV-2 virus after receiving the vaccine.
SARS-CoV-2 Virus (COVID-19) Adenovirus Vector Vaccine: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the SARS-CoV-2 virus vaccine. When feasible, administer indicated vaccines prior to initiating immunosuppressant medications. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure to SARS-CoV-2 virus after receiving the vaccine.
SARS-CoV-2 Virus (COVID-19) mRNA Vaccine: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the SARS-CoV-2 virus vaccine. When feasible, administer indicated vaccines prior to initiating immunosuppressant medications. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure to SARS-CoV-2 virus after receiving the vaccine.
SARS-CoV-2 Virus (COVID-19) Recombinant Spike Protein Nanoparticle Vaccine: (Moderate) Patients receiving immunosuppressant medications may have a diminished response to the SARS-CoV-2 virus vaccine. When feasible, administer indicated vaccines prior to initiating immunosuppressant medications. Counsel patients receiving immunosuppressant medications about the possibility of a diminished vaccine response and to continue to follow precautions to avoid exposure to SARS-CoV-2 virus after receiving the vaccine.
Smallpox and Monkeypox Vaccine, Live, Nonreplicating: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Smallpox Vaccine, Vaccinia Vaccine: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Tofacitinib: (Major) Concomitant use of tofacitinib with biologic immunosuppressants, such as ixekizumab, is not recommended because of the possibility of additive immunosuppression and increased infection risk. Tofacitinib may be used as monotherapy or concomitantly with methotrexate or other nonbiologic DMARDs.
Typhoid Vaccine: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Upadacitinib: (Major) Do not use upadacitinib in combination with biologic immunosuppressives, such as ixekizumab, because of the possibility of increased immunosuppression and increased infection risk. Upadacitinib may be used as monotherapy or concomitantly with methotrexate or other nonbiologic DMARDs. Most patients taking upadacitinib who developed serious infections were taking concomitant immunosuppressives such as methotrexate or corticosteroids.
Varicella-Zoster Virus Vaccine, Live: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Yellow Fever Vaccine, Live: (Major) Do not administer live vaccines to ixekizumab recipients. Before initiation of ixekizumab therapy, consider completion of all age appropriate vaccinations per current immunization guidelines. No data are available on the response to live or inactive vaccines in patients receiving Ixekizumab therapy.
Ixekizumab is a human IgG4 monoclonal antibody that selectively binds to the interleukin 17A (IL-17A) cytokine, inhibiting its interaction with the IL-17 receptor. A naturally occurring cytokine, IL-17A is involved in normal inflammatory and immune responses. Treatment with ixekizumab inhibits the release of proinflammatory cytokines and chemokines.
Ixekizumab is administered subcutaneously. The mean volume of distribution in patients with plaque psoriasis is 7.11 L (29%). Although the metabolic pathway is not fully elucidated, ixekizumab is expected to be degraded to small peptides and amino acids via catabolic pathways in the same manner as endogenous human IgG. Mean systemic clearance is 0.39 L/day, and the mean half-life is 13 days. Ixekizumab exhibits dose-proportional pharmacokinetics in patients with plaque psoriasis over a dose range from 5 mg (not recommended) to 160 mg following subcutaneous administration. The pharmacokinetics of ixekizumab was similar in adult patients with plaque psoriasis, psoriatic arthritis, ankylosing spondylitis, and non-radiographic axial spondyloarthritis.
Affected cytochrome P450 (CYP450) isoenzymes and drug transporters: CYP2D6
Data from drug interaction studies found no clinical significant changes in the exposure of caffeine (CYP1A2 substrate), warfarin (CYP2C9 substrate), omeprazole (CYP2C19 substrate), or midazolam (CYP3A substrate) when used concurrently with ixekizumab as a single 160 mg dose or multiple doses of 80 mg every 2 weeks. The potential effect of ixekizumab on CYP2D6 activity cannot be ruled out due to high variability in exposure (approximately +/- 2-fold) of dextromethorphan and its CYP2D6 metabolite dextrorphan.
-Route-Specific Pharmacokinetics
Subcutaneous Route
Ixekizumab bioavailability ranges from 60% to 81% following subcutaneous administration in patients with plaque psoriasis. Administration via injection in the thigh achieved higher bioavailability compared to that seen with other injection sites including the arm and abdomen. The peak mean (+/- SD) serum concentration of ixekizumab after a subcutaneous doses of 160 mg is 16.2 +/- 6.6 mcg/mL and is reached in approximately 4 days. Following multiple subcutaneous doses of 160 mg ixekizumab, the mean (+/- SD) serum trough concentration at week 8 is 9.3 +/- 5.3 mcg/mL. Steady-state concentrations are achieved by week 10 after switching from the 80 mg every 2 weeks regimen to the 80 mg every 4 weeks dosing regimen at week 12 at which the mean (+/- SD) steady state trough concentration is 3.5 +/- 2.5 mcg/mL.
-Special Populations
Hepatic Impairment
No formal trial of the effect of hepatic impairment on the pharmacokinetics of ixekizumab was conducted.
Renal Impairment
No formal trial of the effect of renal impairment on the pharmacokinetics of ixekizumab was conducted.
Pediatrics
The pharmacokinetics of ixekizumab were evaluated in pediatric psoriasis subjects (age 6 to 17 years) using the recommended pediatric dosing regimen for 12 weeks. For drug recipients weighing more than 50 kg and 25 to 50 kg, the mean steady-state trough concentrations were 3.8 +/- 2.2 mcg/mL and 3.9 +/- 2.4 mcg/mL at week 12, respectively. Data from subjects weighing less than 25 kg (n = 2) were limited.
Geriatric
The clearance of ixekizumab is not significantly influenced by age in adults with plaque psoriasis.
Obesity
The clearance and volume of distribution of ixekizumab increases with increasing body weight.