Imuldosa (ustekinumab-srlf) is a prescription medication approved by the U.S. Food and Drug Administration (FDA) to treat adults and children ages 6 and older with moderate to severe plaque psoriasis.
Imuldosa is a monoclonal antibody, which is a lab-made protein. It binds to two immune system proteins called interleukin-12 and interleukin-23. These proteins are involved in inflammation and immune responses.
In plaque psoriasis, blocking these proteins helps reduce inflammation and slow the overactive immune signals that lead to skin plaques.
Imuldosa is a biosimilar of Stelara. This means it is made from living cells and is designed to work like the original medicine. The FDA requires biosimilars to have no meaningful differences in safety or how well they work.
Doctors prescribe Imuldosa for adults and children ages 6 and older with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy. Phototherapy means treatment with ultraviolet light. Systemic therapy means medicine that works throughout the body.
Imuldosa is given as an injection under the skin. It is given at the start, again four weeks later, and then every 12 weeks.
Imuldosa should be used under the guidance and supervision of a healthcare provider. In children, it is recommended that a healthcare provider give the injection. An individual or caregiver may give the injection at home if a healthcare provider decides this is appropriate and provides proper training.
Imuldosa can be injected under the skin in the upper arms, buttocks, thighs, or stomach area. Do not inject it into skin that is tender, bruised, discolored, or hard. Use a different injection site each time.
The recommended dose of Imuldosa for plaque psoriasis in adults is:
For children ages 6 and older, the recommended dose is:
This information is based on the prescribing information, but your healthcare provider may tailor your treatment plan. Always follow their guidance.
In clinical studies of Imuldosa for moderate to severe plaque psoriasis, the most common side effects occurred in about 3 percent to 8 percent of people. These include:
Imuldosa can cause serious side effects that may require immediate medical attention. These include:
Get medical help right away if you think you are having a serious reaction.
Accord BioPharma, the manufacturer of Imuldosa, offers the AccordCares Co-Pay Assistance Program. The AccordCares Co-Pay Assistance Program also offers benefits investigation, prior authorization support and information, billing and coding information, and alternate coverage identification.
To learn more, visit the AccordCares program website, call 866-258-7151.
Before starting Imuldosa, your doctor will check you for active and latent (hidden) tuberculosis (TB).
Before starting Imuldosa, make sure your vaccines are up to date. While taking Imuldosa, you should avoid live vaccines. You should not receive the BCG vaccine for one year before starting Imuldosa, during treatment, or for one year after stopping Imuldosa.
Tell your doctor if anyone in your home needs a live vaccine. Some live vaccines may spread from a household contact to an individual taking Imuldosa.
Tell your doctor if you have any allergies to ustekinumab-srlf or any ingredients in Imuldosa. Do not take Imuldosa if you have had a clinically significant allergic reaction to ustekinumab products or any of the ingredients in Imuldosa.
Tell your doctor about all medicines you take, including prescription drugs, over-the-counter medicines, vitamins, and herbal supplements.
Before starting Imuldosa, tell your doctor if you think you have an infection or have symptoms of infection.
Also tell your doctor if you:
Tell your doctor if you have had nervous system problems in the past. Tell your doctor right away if you have headache, seizures, confusion, or vision changes.
Imuldosa is also FDA-approved to treat psoriatic arthritis, Crohn’s disease, and ulcerative colitis.
If you are pregnant, planning to become pregnant, or breastfeeding while taking Imuldosa, talk with your doctor about the risks and benefits.
These answers are fact-checked by our editorial staff.
How effective is Imuldosa for plaque psoriasis?
In two studies of adults with plaque psoriasis, ustekinumab was compared with placebo (an inactive treatment).
By week 12, 67 percent to 76 percent of people taking ustekinumab reached PASI 75. This means their psoriasis score improved by at least 75 percent. In comparison, 3 percent to 4 percent of people taking placebo reached PASI 75.
By week 12, 59 percent to 73 percent of people taking ustekinumab were rated as “cleared” or “minimal” on the Physician’s Global Assessment. This is a doctor’s rating of psoriasis severity. In comparison, 4 percent of people taking placebo were rated as “cleared” or “minimal.”
How long does Imuldosa take to work for plaque psoriasis?
The clinical study results do not say exactly when people first notice improvement in plaque psoriasis. In the adult plaque psoriasis studies, results were measured at week 12. At that time, more people taking ustekinumab had improved psoriasis scores than people taking placebo.
What tests or monitoring are needed with Imuldosa for psoriasis?
Before starting Imuldosa, your doctor should check you for TB. You should not receive Imuldosa if you have active TB. If you have latent (inactive) TB, it should be treated before you start Imuldosa.
People receiving Imuldosa should be closely monitored and have regular follow-up visits with a healthcare provider.
Your doctor should watch for signs and symptoms of infection, active TB, nonmelanoma skin cancer, and PRES. PRES is a rare brain condition that can cause headache, seizures, confusion, or vision problems.
On MyPsoriasisTeam, people share their experiences with psoriasis, get advice, and find support from others who understand.
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