JANSSEN
The Janssen Pharmaceutical Companies of Johnson & Johnson today announced that the European Commission (EC) has approved the expanded use of STELARA® (ustekinumab) for the treatment of paediatric patients (ages 6–11) with moderate to severe plaque psoriasis. Ustekinumab was previously approved for use in adolescent and adult patients with plaque psoriasis, aged 12 years and older, and is now the first available biologic treatment in this patient population to selectively address the IL‑23/IL‑12 pathway, an important therapeutic target for the condition.1
In one third of the 14 million cases in Europe, psoriasis begins in childhood.2,3 Psoriasis is an immune-mediated inflammatory disease that affects the skin, resulting in areas of red or inflamed skin covered with silvery scales, which are known as plaques.2 The condition can have a profound, long-term impact on the psychological health and overall quality of life for children.3,4 The development of paediatric psoriasis is also associated with high incidence of low self-esteem, and it can have long-term ramifications into adulthood and beyond.5
“This latest EC approval is a significant milestone for young children struggling to cope with the symptoms of psoriasis, ” said Lloyd Miller, Vice President, Immunodermatology Disease Area Leader, Janssen Research & Development, LLC. “We’re delighted that this therapy, which has a well-established safety and efficacy profile in adults with plaque psoriasis and other immune diseases, is now expanded to children as young as six who are living with this chronic disease.”
The EC approval is based on results from the Phase 3 CADMUS Jr study, building on the prior Phase 3 CADMUS study, which found ustekinumab improved the signs and symptoms of plaque psoriasis, as well as health‑related quality of life (HrQOL), in paediatric patients aged six to 11 years old.6,7,8,9,10 The primary endpoint was the proportion of patients who achieved a physician’s global assessment (PGA) score of Cleared (0) or Minimal (1) at week 12. Secondary endpoints included the proportion of patients achieving improvements in psoriasis area and severity index of ≥75% (PASI 75), ≥90% (PASI 90), and change from baseline in Children’s Dermatology Life Quality Index (CDLQI)* at week 12.8
In the study, 44 patients (aged 6–11 years) from nine countries were enrolled and treated with at least one injection of ustekinumab. At baseline, the mean duration of psoriasis was 3.5 (standard deviation 2.49) years. At week 12, subjects treated with ustekinumab showed clinically meaningful improvements in their psoriasis and HrQOL. At week 12, 77.3% (95% confidence interval [CI]: 62.2%, 88.5%) achieved PGA 0/1, 84.1% (95% CI: 69.9%, 93.4%) achieved PASI 75, and 63.6% (95% CI: 47.8%, 77.6%) achieved PASI 90. The mean change from baseline in CDLQI was -6.3 (95% CI: -8.29; -4.28, lower is better). All patients were followed for up to 52 weeks after the first administration of ustekinumab. Improvements in PGA 0/1, PASI 75, PASI 90 and CDLQI were maintained through to week 52 (75.6%, 87.7%, 70.7%, and 58.3%, respectively).6,7
Safety data from CADMUS Jr were consistent with the known safety profiles reflected in respective current prescribing information labels and ustekinumab was generally well‑tolerated by paediatric patients with plaque psoriasis. Overall, 34 patients had more than one adverse event (AE; [77.3%]) and three had more than one serious AE (6.8%). One patient had a serious infection (mononucleosis), 29 had infections (65.9%), and 12 had infections requiring treatment (27.3%). In general, the AEs and other safety data reported up to one year in two paediatric patient studies (CADMUS and CADMUS Jr) were similar to those seen in previous studies in adults with plaque psoriasis.6,7,11,12,13
This marketing authorisation follows a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), issued on 12 December 2019.
#ENDS#
Key definitions
* The Children’s Dermatology Life Quality Index is a 10-item questionnaire designed to measure the impact of any skin disease on the lives of children. A score of 0–1 denotes no impact, whereas a score of ≥19 denotes an extremely large impact. A reduction in this score equates to a reduction in the impact on the life of the child.14
About psoriasis
What it is
Psoriasis is an immune-mediated inflammatory disease that manifests on the skin.15
The most common form of psoriasis is plaque psoriasis, usually resulting in areas of red or inflamed skin covered with silvery scales, which are known as plaques.16
The inconsistent nature of psoriasis means that even when plaques appear to subside, patients can have ongoing concerns over their return.15
Impact
Psoriasis can cause a great physical and psychological burden. Mental health issues are common among people with psoriasis, and the impact it can have on quality of life is comparable to diabetes and cancer.4
Psoriasis is also associated with several comorbidities including psoriatic arthritis, cardiovascular diseases, metabolic syndrome, chronic obstructive pulmonary disorder (COPD) and osteoporosis.17
In addition, many individuals are faced with social exclusion, discrimination and stigma because of their disease.18
Children are a particularly vulnerable patient group, and studies show that psoriasis has a profoundly disruptive effect on forming social relationships and school life.19
About the CADMUS programme
CADMUS Jr is a Phase 3, multicentre, open-label study including 44 participants aged 6–11 years, which was initiated following the successful completion of the CADMUS study involving patients aged 12–17 years. The study included a single arm in which patients received one injection of ustekinumab subcutaneously on weeks 0, 4, 16, 28 and 40. The dose of ustekinumab administered was dependant on the weight of the participant, as follows: Participants weighing <60 kg received ustekinumab 0.75 mg/kg; participants weighing ≥60 kg to ≤100 kg received ustekinumab 45 mg; participants weighing >100 kg received ustekinumab 90 mg. Following completion of the week 52 visit, participants who had a beneficial response from ustekinumab treatment, as determined by the investigator, and who had not yet reached the age of 12 years or older in countries where marketing authorisation for ustekinumab has been granted for the treatment of psoriasis in adolescent participants (12–17 years), and who were willing to continue ustekinumab treatment, could enter the long-term extension (LTE) period (from week 56 through week 264) of the study. The study primarily concluded in December 2017 and the LTE period is ongoing.8
CADMUS is a Phase 3, multicentre, randomised, double-blind study including 110 participants aged 12–17 years. The study included three arms: the ustekinumab standard dosage arm, the ustekinumab half-standard dosage arm, and the placebo arm. In the standard dosage arm (0.75 mg/kg, 45 mg, or 90 mg [based on body weight]), patients received one injection of ustekinumab subcutaneously on weeks 0, 4, 16, 28 and 40, and received one placebo injection subcutaneously on weeks 0 and 4 or week 12. In the half-standard dosage arm (0.375 mg/kg, 22.5 mg, or 45 mg [based on body weight]), patients received one injection of ustekinumab subcutaneously on weeks 0, 4, 16, 28 and 40, and received one placebo injection subcutaneously on weeks 0 and 4 or week 12. In the placebo arm, patients received one placebo injection subcutaneously on weeks 0 and 4 or week 12, followed by ustekinumab at half‑standard or standard dosage at weeks 12, 16, 28, and 40. The study concluded in January 2014.9
The primary endpoint of both studies was the percentage of participants achieving a PGA score of Cleared (0) or Minimal (1) at week 12. Safety data from CADMUS Jr and CADMUS were consistent with the known safety profiles reflected in respective current prescribing information labels, and ustekinumab was generally well‑tolerated by paediatric patients with plaque psoriasis. Overall for CADMUS Jr, 34 patients had more than one AE (77.3%) and three had more than one serious AE (6.8%). One patient had a serious infection (mononucleosis), 29 had infections (65.9%), and 12 had infections requiring treatment (27.3%). For CADMUS, 90 patients (81.8%) reported an AE, of which 34.5% reported nasopharyngitis, 12.7% reported an upper respiratory tract infection, and 8.2% reported pharyngitis. 74 (67.3%) reported an infection and two serious infections were reported (pyelonephritis and ear infection). In general, the AEs and other safety data reported up to 1 year in both paediatric patient studies were similar to those seen in studies in adults with plaque psoriasis.6,7,10,11,12,13
About STELARA® (ustekinumab) 6
In the European Union (EU), ustekinumab is approved for the treatment of moderate to severe plaque psoriasis in children and adolescent patients aged six years and older who are inadequately controlled by or are intolerant to other systemic therapies or phototherapies, and is also approved for the treatment of moderate to severe plaque psoriasis in adults who failed to respond to, have a contraindication to, or are intolerant to other systemic therapies including cyclosporine, methotrexate (MTX) or psoralen plus ultraviolet A. In addition to psoriasis, ustekinumab has also been approved for the treatment of three further immune-mediated conditions in the EU: psoriatic arthritis, Crohn's disease (CD) and ulcerative colitis (UC).
Ustekinumab is approved alone or in combination with MTX for the treatment of active psoriatic arthritis in adult patients when the response to previous non-biological disease-modifying antirheumatic drug therapy has been inadequate. Ustekinumab is also approved for the treatment of adults with moderately to severely active UC who have had an inadequate response with, or lost response to, or were intolerant to either conventional therapy or a biologic, or have medical contraindications to such therapies. Moreover, ustekinumab is approved for the treatment of adult patients with moderate to severe CD who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a TNF‑alpha antagonist, or have medical contraindications to such therapies.
The Janssen Pharmaceutical Companies of Johnson & Johnson maintain exclusive worldwide marketing rights to STELARA® .
Important safety information 6
The most common AEs (>5%) in controlled periods of clinical studies with ustekinumab were nasopharyngitis and headache. Most were considered to be mild and did not necessitate discontinuation of study treatment. The most serious adverse reaction that has been reported for ustekinumab is serious hypersensitivity reactions, including anaphylaxis. The overall safety profile is similar for adult patients with psoriasis, psoriatic arthritis, CD and UC.
Please refer to the Summary of Product Characteristics for full prescribing information for ustekinumab:
https://www.ema.europa.eu/en/medicines/human/EPAR/stelara
About the Janssen Pharmaceutical Companies of Johnson & Johnson
At Janssen, we’re creating a future where disease is a thing of the past. We’re the Pharmaceutical Companies of Johnson & Johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Hypertension.
Learn more at www.janssen.com/emea . Follow us at www.twitter.com/JanssenEMEA .
Janssen-Cilag International NV, the marketing authorisation holder for STELARA® in the EU, and Janssen Research & Development, LLC, are part of the Janssen Pharmaceutical Companies of Johnson & Johnson.
Cautions concerning forward-looking statements
This press release contains "forward-looking statements" as defined in the Private Securities Litigation Reform Act of 1995 regarding development and potential availability in the EU of STELARA® (ustekinumab). The reader is cautioned not to rely on these forward-looking statements. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or known or unknown risks or uncertainties materialise, actual results could vary materially from the expectations and projections of Janssen-Cilag International NV, and any of the other Janssen Pharmaceutical Companies and/or Johnson & Johnson. Risks and uncertainties include, but are not limited to: challenges and uncertainties inherent in product research and development, including the uncertainty of clinical success and of obtaining regulatory approvals; uncertainty of commercial success; manufacturing difficulties and delays; competition, including technological advances, new products and patents attained by competitors; challenges to patents; product efficacy or safety concerns resulting in product recalls or regulatory action; changes in behaviour and spending patterns of purchasers of health care products and services; changes to applicable laws and regulations, including global health care reforms; and trends toward health care cost containment. A further list and descriptions of these risks, uncertainties and other factors can be found in Johnson & Johnson's Annual Report on Form 10-K for the fiscal year ended 30 December, 2018, including in the sections captioned “Cautionary Note Regarding Forward-Looking Statements” and “Item 1A. Risk Factors,” and in the company’s most recently filed Quarterly Report on Form 10-Q, and the company’s subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at www.sec.gov , www.jnj.com or on request from Johnson & Johnson. None of the Janssen Pharmaceutical Companies nor Johnson & Johnson undertakes to update any forward-looking statement as a result of new information or future events or developments.
# # #
References
1 Benson J, et al . Discovery and mechanism of ustekinumab. MAbs 2011;3:535–45.
2 Ortonne J and Prinz J. Alefacept: A novel and selective biologic agent for the treatment of chronic psoriasis. Eur J Dermatol 2004;14:41–5.
3 Bronckers I, et al . Psoriasis in children and adolescents: diagnosis, management and comorbidities. Paediatr Drugs 2015;17:373–84.
4 Bajorek Z, et al . The impact of long term conditions on employment and the wider UK economy. The Work Foundation 2016. Available at: http://www.theworkfoundation.com/wp-content/uploads/2016/11/397_The-impact-of-long-term-conditions-on-the-economy.pdf . (last accessed January 2020).
5 Salman A, et al . Impact of psoriasis in the quality of life of children, adolescents and their families: a cross-sectional study. An Bras Dermatol 2018;93:819–23.
6 European Medicines Agency. STELARA Summary of product characteristics. 2020. Available at: https://www.medicines.org.uk/emc/product/4413/smpc . (last accessed January 2020).
7 Phillip S, et al . Ustekinumab for the treatment of moderate-to-severe plaque psoriasis in paediatric patients. Presented at Skin Inflammation and Psoriasis International Network (SPIN), Paris, France, 25–27 April 2019 (poster abstract P025).
8 ClinicalTrials.gov. An efficacy, safety, and pharmacokinetics study of subcutaneously administered ustekinumab in the treatment of moderate to severe chronic plaque psoriasis in pediatric participants greater than or equal to 6 to less than 12 years of age (CADMUS Jr). Identifier NCT02698475. Available at: https://clinicaltrials.gov/ct2/show/NCT02698475 . (last accessed January 2020).
9 ClinicalTrials.gov. A study of the safety and efficacy of ustekinumab in adolescent patients with psoriasis (CADMUS). Identifier NCT01090427. Available at: https://clinicaltrials.gov/ct2/show/NCT01090427 . (last accessed January 2020).
10 Landells I, et al . Ustekinumab in adolescent patients age 12 to 17 years with moderate-to-severe plaque psoriasis: Results of the randomized phase 3 CADMUS study. J Am Acad Dermatol 2015;43:594–603.
11 Papp K, et al . Safety surveillance for ustekinumab and other psoriasis treatments from the Psoriasis Longitudinal Assessment and Registry (PSOLAR). J Drugs Dermatol 2015;14(7):706–14.
12 Leonardi C, et al . Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 76-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 1). Lancet 2008;371:1665–74.
13 Papp K, et al . Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 52-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 2). Lancet 2008;371:1675–84.
14 Cardiff University School of Medicine. Children’s Dermatology Life Quality Index. Available at: https://www.cardiff.ac.uk/medicine/resources/quality-of-life-questionnaires/childrens-dermatology-life-quality-index . (last accessed January 2020).
15 Clark RA. Resident memory T cells in human health and disease. Sci Transl Med 2015;7:269rv1.
16 British Skin Foundation. Psoriasis. Available at: www.britishskinfoundation.org.uk/SkinInformation/AtoZofSkindisease/Psoriasis.aspx (last accessed January 2020).
17 Nijsten T and Wakkee M. Complexity of the association between psoriasis and comorbidities. J Invest Dermatol 2009;129:1601–3.
18 World Health Organization. Global Report on Psoriasis. 2016. Available at: apps.who.int/iris/bitstream/10665/204417/1/9789241565189_eng.pdf . (last accessed January 2020).
19 De Jager M, et al . The burden of childhood psoriasis. Pediatr Dermatol 2011;28:736–7.
CP-134948
January 2020
View source version on businesswire.com: https://www.businesswire.com/news/home/20200123005269/en/
About Business Wire
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Dubai Brings Together Sport Stars and Legends, Leaders and Decision-Makers on the Largest Global Platform to Shape the Future of Sports: the World Sports Summit18.12.2025 14:40:00 CET | Press release
Under the directives of His Highness Sheikh Hamdan bin Mohammed bin Rashid Al Maktoum and the supervision of the Dubai Sports Council- The Summit, under the theme ‘Uniting the World Through Sports’, aligns with the objectives of Dubai Sports Sector Strategic Plan 2033- A comprehensive programme will address the future of sports, development of the sector and more The Dubai Sports Council has announced the launch of the World Sports Summit (WSS), which will take place under the directives of His Highness Sheikh Hamdan bin Mohammed bin Rashid Al Maktoum, Crown Prince of Dubai, Deputy Prime Minister, Minister of Defence and Chairman of the Executive Council of Dubai. The event is set to be held from December 29-30, 2025 at Madinat Jumeirah in Dubai, under the theme ‘Uniting the World Through Sports’. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251218607571/en/ Dubai Brings Together Sport Stars and Legends, Leaders and Decisi
Regula Wins High Customer Marks and Strong Momentum in G2’s Winter 2026 Grid Reports for Identity Verification18.12.2025 14:11:00 CET | Press release
Regula, a global developer of identity verification solutions, has been recognized by customers on G2’s review platform as one of the fastest-rising and most trusted vendors in the identity verification market. Regula is named as a Leader in three G2 Winter 2026 Grid® Reports for Identity Verification. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251218134153/en/ Regula is recognized as a Leader in G2’s Winter 2026 Grid Reports for Identity Verification, reflecting strong customer satisfaction and enterprise-grade IDV capabilities. This season, Regula earned a Leader placement in G2’s Overall Grid® for Identity Verification Software, reflecting strong customer satisfaction and a growing presence in the market. The company was also named a Leader in the Momentum Grid® Report for Identity Verification, highlighting accelerating demand for Regula’s solutions and increasingly positive feedback from users. In addition, Regula a
Aptiv and Vecna Robotics to Develop Next Generation Autonomous Mobile Robots18.12.2025 14:00:00 CET | Press release
Collaboration to Deliver Safer, Smarter, and Cost-Effective Automation for Warehouses and Factories Aptiv PLC (NYSE: APTV), a global industrial technology leader, and Vecna Robotics, a pioneer in AI-driven autonomous material handling solutions, today announced a strategic collaboration to co-develop next-generation Autonomous Mobile Robot (AMR) solutions designed to deliver cost-efficient automation. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251218958100/en/ Aptiv’s advanced perception portfolio and machine learning technologies will be integrated into Vecna Robotics’ platform. This partnership combines Aptiv’s industry-leading portfolio, with Vecna Robotics’ advanced autonomy and orchestration platform to provide safer, more efficient, and scalable material handling systems. “Automation is transforming the way goods move through warehouses and factories, with devices that sense, think and act in real time,” said Javed
Syremis Therapeutics Launches with $165M to Develop Best-in-Class Medicines for Mental Health Conditions18.12.2025 14:00:00 CET | Press release
Addressing major unmet needs in mental health with pharmacology rooted in emerging and clinically validated neuropsychiatric biologyLead program ST-905, a potent M1/M4 muscarinic agonist, currently in Phase 1 clinical developmentSecond program ST-901, a novel NMDA antagonist, currently in IND-enabling studies and expected to enter Phase 1 development next yearSeries A co-led by Dexcel Pharma and Third Rock Ventures with participation from Bain Capital Life Sciences, GV (Google Ventures), QVT, and Pictet Syremis Therapeutics, a clinical-stage biopharmaceutical company developing novel medicines to make a profound impact on the treatment of mental health, today announced its launch with a $165 million financing. The Series A, co-led by Dexcel Pharma and Third Rock Ventures, with participation from Bain Capital Life Sciences, GV (Google Ventures), QVT, and Pictet will support the advancement of Syremis’ pipeline through clinical proof of concept. Schizophrenia and other psychotic disorder
BeOne Medicines Granted U.S. FDA Fast Track Designation for BGB-B2033 as Treatment for Hepatocellular Carcinoma18.12.2025 12:00:00 CET | Press release
BGB-B2033 is a bispecific antibody directed at GPC3 and 4-1BB; key targets in the most common liver cancerFDA Fast Track Designation reflects the potential of BGB-B2033 in an area of high unmet need BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the U.S. Food and Drug Administration (FDA) has granted the Company Fast Track Designation for BGB-B2033, its GPC3x4-1BB bispecific antibody for the treatment of adult patients with hepatocellular carcinoma (HCC) with disease progression on or after prior systemic treatment. “The FDA awards Fast Track Designation to therapies that show potential to address an unmet medical need in serious or life-threatening conditions. The FDA’s decision reflects the encouraging profile of BGB-B2033 in advanced hepatocellular carcinoma, where patients continue to face limited treatment options,” said Julie Lepin, Senior Vice President and Chief Regulatory Affairs Officer at BeOne. BeOne is currentl
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
