Eligible patients had Psoriasis Area Severity Index (PASI) ≥12, Physician Global Assessment (PGA) ≥3, and Body Surface Area (BSA) involvement ≥10%, were candidates for phototherapy or systemic therapy, and had disease that was inadequately controlled by topical therapy. 25 subQ injection maintenance doses of 40 mg (1 every other week thereafter)
Evaluate patients for TB prior to initiating treatment with STELARA Stelara Dosage Psoriasis. Missing data last observation carried forward rules were applied. For optimal outcome, STELARA® should be dosed and administered as described in the PSUMMIT II was a multicenter, randomized, double-blind, placebo-controlled study in 312 adult patients with active PsA for ≥6 months, despite current or previous DMARD and/or NSAID therapy, and who may have been previously treated with biologic anti-TNF agent(s). CD=Crohn's disease; IV=intravenous; subQ=subcutaneous. CDAI=Crohn's Disease Activity Index; IV=intravenous; LTE=long-term extension; subQ=subcutaneous; TNF=tumor necrosis factor. One case of reversible posterior leukoencephalopathy syndrome (RPLS) was observed in clinical studies of psoriasis and psoriatic arthritis. For patients weighing 100 kg or less, the recommended dose is 45 mg initially and 4 weeks later, followed by... Psoriatic Arthritis. Cumulative overall safety was evaluated during the placebo-controlled period (12 or 20 weeks) and up to 5 years of treatment. Please refer to each product’s Prescribing Information for recommended dosing and administration. STELARA® Recommended Dosing for CD: Induction dose—A single IV infusion using a weight-based dosage regimen: 260 mg (weight ≤55 kg), 390 mg (weight >55 kg to 85 kg), 520 mg (weight >85 kg).
Do not freeze. Humira® is a registered trademark of AbbVie Inc. Of all the plaque psoriasis biologic medications, STELARA® has the fewest yearly doses. Single IV induction dose administered over at least 1 hour Primary endpoint was PGA score of 0 or 1 at Week 12; major secondary endpoints were PASI 75 response and PASI 90 response at Week 12. DOSING AND ADMINISTRATION GUIDE FOR STELARA® IN CROHN’S DISEASE STELARA® treatment continues with a subcutaneous (subQ) 90-mg dose 8 weeks after the initial IV dose, then every 8 weeks thereafter.
It is not known whether patients with pharmacologic blockade of IL-12/IL-23 from treatment with STELARA® may be susceptible to these types of infections. No cases of RPLS were observed in clinical studies of Crohn’s disease or ulcerative colitis. © Janssen Biotech, Inc. 2020. There is a pregnancy registry that monitors pregnancy outcomes in women exposed to STELARA® during pregnancy. Third party trademarks used herein are trademarks of their respective owners. This is not intended to compare the safety, effectiveness, or uses of these treatments.
Storage time at room temperature begins once the diluted solution has been prepared. 3 starter injections of
The Prescribing Information included here may not be appropriate for use outside the United States and Puerto Rico. Infections Individuals genetically deficient in IL-12/IL-23 are particularly vulnerable to disseminated infections from mycobacteria, Salmonella, and Bacillus Calmette-Guerin (BCG) vaccinations. To start, you’ll get doses at weeks 0, 4, and then every 12 weeks after that. The most common adverse reactions (≥3% and higher than that with placebo) in adults from psoriasis clinical studies for STELARA Select one or more newsletters to continue. To learn more about prescribing STELARA® STELARA ® is a 45 mg or 90 mg injection given under the skin, as directed by your doctor. Clicking on “Yes” below will take you to a website to which our site’s For the treatment of adult patients with moderately to severely active CD 6 subQ maintenance doses during Year 1 All rights reserved. …
This site is published by Janssen Biotech, Inc., which is solely responsible for its contents. To prevent premature activation of the needle safety guard, do not touch the NEEDLE GUARD ACTIVATION CLIPS at any time during use.Do not hold the PLUNGER or PLUNGER HEAD while removing the NEEDLE COVER or the PLUNGER may move.
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