Ustekinumab


Ustekinumab, sold under the brand name Stelara, is a human monoclonal antibody used to treat psoriasis. It is also approved to treat Crohn's disease in the United States, Israel and Australia, and ulcerative colitis in the U.S., and in the European Union among people who have not responded to more traditional treatments. It was found not effective for multiple sclerosis.
It is manufactured in the Netherlands. It is a subcutaneous human interleukin 12 and interleukin 23 antagonist. These are naturally occurring proteins that regulate the immune system and immune-mediated inflammatory disorders.

Medical uses

Ustekinumab is used to treat psoriasis. This includes psoriatic arthritis when it affects the skin. It is indicated for the treatment of adult and adolescent patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy, and adult patients with active psoriatic arthritis alone or in combination with methotrexate. It is also used to treat moderately to severely active Crohn's disease and moderately to severely active ulcerative colitis.
In the European Union, Ustekinumab is approved to treat moderate to severe plaque psoriasis in adults and children above the age of six years whose condition has not improved with, or who cannot use, other systemic psoriasis treatments, such as ciclosporin, methotrexate or PUVA ; active psoriatic arthritis in adults; moderately to severely active Crohn's disease in adults; and moderately to severely active ulcerative colitis in adults.

Adverse effects

According to information provided by Centocor, maker of one medication based on ustekinumab, their version of the drug is associated with several types of serious adverse effects. These include an increased risk of infection, such as by tuberculosis and an increased risk of certain types of cancer. As with some other immunosuppressant drugs like ciclosporin, the brain swelling of posterior reversible encephalopathy syndrome is a risk. The pharmaceutical company also reports serious allergic reaction as a possible side effect. More common side effects are upper respiratory infection, headache, and tiredness.
Clinical trials have shown that subcutaneous ustekinumab was generally well tolerated. Most treatment-emergent adverse events were of mild severity.

Pregnancy

It is unknown if the medication is safe during pregnancy or breastfeeding.

Mechanism of action

Ustekinumab is designed to interfere with the triggering of the body's inflammatory response through the suppression of certain cytokines. Specifically, it blocks interleukin IL-12 and IL-23 which help activate certain T-cells. It binds to the p-40 subunit of both IL-12 and IL-23 so that they subsequently cannot bind to their receptors.

History

, there were 5 NIH-listed research studies involving CNTO 1275 on a multinational basis, including 3 Phase II and 2 Phase III trials. Three studies were focused on patients with psoriasis, one on psoriatic arthritis, and one on multiple sclerosis.
On December 4, 2007, a Biologic License Application with the U.S. Food and Drug Administration was filed by Centocor and Janssen-Cilag International has submitted a Marketing Authorization Application to the European Medicines Agency.
On November 21, 2008, the European Medicines Agency's Committee for Medicinal Products for Human Use adopted a positive opinion for ustekinumab for the treatment of moderate to severe plaque psoriasis in adult patients who failed to respond to other systemic therapies.

Approvals

Since 2009, Ustekinumab is approved in Canada, Europe and the United States to treat moderate to severe plaque psoriasis. On September 24, 2013, the U.S. Food and Drug Administration approved the use of ustekinumab for the treatment of psoriatic arthritis.
On December 12, 2008 the Canadian Health Authority approved the use of ustekinumab for the treatment of chronic moderate to severe plaque psoriasis in adult patients who are candidates for phototherapy or systemic therapy.
The FDA approved the drug on September 25, 2009 for the treatment of adult patients with moderate to severe plaque psoriasis.
The FDA approved the drug in September 2016 for the treatment of Crohn's disease.
Since September 2017, ustekinumab is available on the Pharmaceutical Benefits Scheme for the treatment of severe Crohn's disease in adults.
In 2019, the European Commission approved the use of ustekinumab for adults with moderately to severely active ulcerative colitis.
In October 2019, the FDA approved the use of ustekinumab for adults with moderately to severely active ulcerative colitis.