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(uss-te-kin-oo-mab) ,


(trade name)


Therapeutic: antipsoriatics
Pharmacologic: interleukin antagonists
Pregnancy Category: B


Moderate to severe plaque psoriasis in patients who are candidates for phototherapy or systemic therapy.Active psoriatic arthritis (as monotherapy or with methotrexate)


Binds to the p40 protein subunit used by both the interleukin (IL)-12 and IL-23 cytokines. These cytokines that are involved in inflammatory and immune responses, including natural killer cell activation and CD4+ T-cell differentiation and activation. Binding to interleukins antagonizes their effects, disrupting IL-12 and IL-23 mediated signaling and cytokine cascades.

Therapeutic effects

Decrease in area and severity of psoriatic lesions.
Decreased progression of psoriatic arthritis


Absorption: Well absorbed following subcutaneous administration.
Distribution: Unknown.
Metabolism and Excretion: Broken down by catabolic processes into peptides and amino acids.
Half-life: 15–46 days.

Time/action profile

45 mg subcutunknown13.5 days12 wk
90 mg subcutunknown7 days12 wk
†Blood levels


Contraindicated in: HypersensitivityActive untreated infection.
Use Cautiously in: History of known malignancy or tuberculosis (possibility of reactivation); >60 yr, history of prolonged immunosuppressant therapy, or history of PUVA treatment (↑ risk of skin cancer) Obstetric: Use only if potential benefit justifies potential risk to the fetus.; Lactation: Unknown risks to infant from gastrointestinal/systemic exposure should be weighed against known benefits of breast-feeding.; Pediatric: Safety and effectiveness not established.
Exercise Extreme Caution in: Chronic infection or history of recurrent infection.

Adverse Reactions/Side Effects

Central nervous system

  • Reversible Posterior Leukoencephalopathy Syndrome (life-threatening)
  • fatigue (most frequent)
  • headache (most frequent)


  • erythema


  • anaphylaxis (life-threatening)
  • angioedema (life-threatening)
  • infection (life-threatening)
  • malignancy (life-threatening)


Drug-Drug interaction

May ↓ antibody response to and ↑ risk of adverse reactions from live vaccines.May ↓ desired antibody response to non-live vaccines.May affect the activity of CYP450 drug-metabolizing enzymes; when treatment is started during concurrent CYP450 substrates, especially those with a narrow therapeutic indices, including warfarin and cyclosporine ; appropriate monitoring and dose adjustment should be carried out.



Subcutaneous (Adults ≤100 kg) 45 mg initially and 4 wk later, then 45 mg q 12 wk.
Subcutaneous (Adults >100 kg) 90 mg initially and 4 wk later, then 90 mg q 12 wk.

Psoriatic Arthritis

Subcutaneous (Adults) 45 mg initially and 4 wk later, then 45 mg q 12 wk.
Subcutaneous (Adults >100 kg with concomitant moderate-severe plaque psoriasis) 90 mg initially and 4 wk later, then 90 mg q 12 wk.


Solution for subcutaneous injection: 45 mg/0.45 mL in single-use vials and prefilled syringes, 90 mg/mL in single-use vials and prefilled syringesvial

Nursing implications

Nursing assessment

  • Assess affected area(s) prior to and periodically during therapy.
  • Assess for signs of infection (fever, dyspnea, flu-like symptoms, frequent or painful urination, redness or swelling at the site of a wound), including tuberculosis, prior to injection. Ustekinumab is contraindicated in patients with active infection. New infections should be monitored closely; most common are upper respiratory tract infections, bronchitis, and urinary tract infections. Infections may be fatal, especially in patients taking immunosuppressive therapy. genetic implication Patients genetically deficient in IL-12/IL-23 are particularly vulnerable to disseminated infections; diagnostic testing should be considered.
  • Assess patient for latent tuberculosis with a tuberculin skin test prior to initiation of therapy. Treatment of latent tuberculosis should be started before therapy with ustekinumab.
  • Monitor for signs and symptoms of hypersensitivity reaction and anaphylaxis (rash, chest tightness, feeling faint, difficulty breathing, throat tightness, swelling of face, eyelids, tongue, or throat) during therapy.

Potential Nursing Diagnoses

Impaired skin integrity (Indications)


  • Administer a tuberculin skin test prior to administration of ustekinumab. Patients with active latent TB should be treated for TB prior to therapy.
    • Immunizations should be current prior to initiating therapy. Patients on ustekinumab may receive concurrent vaccinations, except for live vaccines.
  • Subcutaneous: Administer using a 27 gauge, 1/2 inch needle in upper arm, gluteal region, thigh, or abdomen; rotate site. Do not administer in areas that are tender, bruised, erythematous, or indurated. Solution is colorless to light yellow and may contain a few small translucent or white particles; do not administer solutions that are discolored, cloudy, or contain other particulate matter. Do not shake. Store solution in refrigerator; do not freeze.

Patient/Family Teaching

  • Instruct patient on correct technique for self-injection, care and disposal of equipment. Review Medication Guide with patient before starting therapy and with each injection.
  • Inform patient that ustekinumab may lower ability to fight and increase risk for infections. Advise patient to notify health care professional immediately if signs of anaphylaxis or infection (fever, sweats, chills, muscle aches, cough, shortness of breath, blood in phlegm, weight loss, warm, red, or painful sores, diarrhea or stomach pain, burning or urination or urinary frequency, tiredness) occur.
  • Inform patient that ustekinumab may increase for cancer. Advise patient to obtain preventative screening.
  • Advise patient to notify health care professional if signs of reversible posterior leukiencephalopathy syndrome (headache, seizures, confusion, visual problems) occur.
  • Instruct patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and consult health care professional before taking any new medications.
  • Instruct patient to notify health care professional of medication regimen prior to treatment or surgery.
  • Advise female patient to notify health care professional if pregnancy is planned or suspected or if breastfeeding.

Evaluation/Desired Outcomes

  • Decrease in extent and severity of psoriatic lesions.
  • Decreased progression of psoriatic arthritis
References in periodicals archive ?
Janssen announced the submission of a supplemental Biologics License Application to the US Food and Drug Administration seeking approval of Stelara for the treatment of adults with moderately to severely active ulcerative colitis in December 2018.
Frohlich was vice president of business development at Arbutus Biopharma, and prior to that worked internationally at Johnson & Johnson and Merck in various roles leading commercial strategy across all stages of product development including the global launches of INCIVO (telaprevir) and STELARA (ustekinumab).
Bio-Thera Solutions is also pursuing biosimilar versions of Humira and Stelara.
Based on drug, the dermatology drugs market has been mainly classified into Humira, Remicade, Otezla, Stelara, Enbrel, Cosentyx, Neoral, Taltz, Cubicin, Canesten, Zyvox, Dupixent, Protopic, Valtrex, and Eucrisa.
Results from the Phase 3 UNIFI study evaluating the efficacy and safety of STELARA (ustekinumab) in patients with moderate to severe ulcerative colitis (UC) one in the overall UC population and a second in patients who previously failed biologic therapy and those who had not previously failed a biologic therapy will be shared in oral presentations on May 21.
Patients with psoriasis or psoriatic arthritis (PsA) treated with ustekinumab (Stelara) or a tumor necrosis factor (TNF) inhibitor had no differences in the overall risks of incident atrial fibrillation (AFib) or major adverse cardiovascular events (MACE), according to authors of a cohort study.
Then the company produced more advanced medicines such as Stelara, which proved efficiency in treating many diseases such as psoriasis, the thing that led the company's direction towards producing a special treatment that summarizes the largest and most recent researches and studies of the company in treating psoriasis: TremfyaA (Guselkumab).
Fahad Al-Najjar KUWAIT, April 1 (KUNA) -- Ministry of Health announced Monday that it is providing ustekinumab (Stelara) fusions and injections for severe crohn's patients.
In a head-to-head study with a similar drug called Stelara, 75 percent of those treated with Skyrizi achieved a 90% improvement, compared with just 42 percent of those given the popular standard treatment.
Results for the year, excluding the impact of acquisitions and divestitures, were driven by STELARA, up 29% to $5.2 billion, and SIMPONI/SIMPONI ARIA, up 14% to $2.1 billion, ZYTIGA, up 40% to $3.5 billion, DARZALEX, up 63% to $2.0 billion, IMBRUVICA, up 38% to $2.6 billion, TREMFYA with sales of $544 million, INVEGA SUSTENNA/XEPLION/INVEGA up 14% to $2.9 billion, partially offset by declines in REMICADE, down 16% to $5.3 billion due to biosimilar competition.
* Biologies: Infliximab (Remicade), adalimumab (Humira), golimumab (Simponi), and certolizumab (Cimzia), natalizumab (Tysabri), ustekinumab (Stelara), and vedolizumab (Entyvio)
M2 EQUITYBITES-October 11, 2018-Janssen Pharmaceutical's Stelara single dose succeeds in phase three ulcerative colitis study