STELARA® (ustekinumab) Data Demonstrate Long-term Efficacy and Safety Results in Adults With Moderately to Severely Active Ulcerative Colitis in Phase 3 Extension Trial
The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new two-year data from the long-term extension of the Phase 3 UNIFI study, demonstrating the efficacy and safety of ustekinumab through two years of treatment in adults with moderately to severely active ulcerative colitis (UC). These data are being presented today as a late-breaking data presentation (LB01) at the 27th UEGW congress.1
These data include 399 participants who were in clinical response eight weeks after receiving a single intravenous (IV) induction dose of ustekinumab and who were then randomised to receive ustekinumab subcutaneous (SC) 90 mg injections every 12 weeks (q12w), ustekinumab SC 90 mg injections every 8 weeks (q8w), or placebo, and who were treated in the long-term extension.1
Results showed that the majority of patients were able to sustain remission through to week 92 as assessed by symptomatic remission. The percentage of patients receiving ustekinumab SC who were in symptomatic remission between weeks 44 and 92 ranged from 83 to 90 percent.1 Among patients who had achieved clinical remission at maintenance baseline, 69 percent of patients receiving ustekinumab q8w and 80 percent of patients receiving ustekinumab q12w maintained symptomatic remission at both weeks 44 and 92. Additional analyses demonstrated that approximately 60 percent of patients receiving ustekinumab q8w and q12w achieved corticosteroid-free symptomatic remission at week 92 (64.3 percent and 63.8 percent, respectively).1
“Ulcerative colitis is a life-long and debilitating inflammatory bowel disease, interrupting the daily lives of millions of people around the world who may still be searching for an effective treatment option,” said lead study investigator Bruce E. Sands, M.D., Icahn School of Medicine, Mt. Sinai, New York, who will be delivering the oral presentation. “It’s encouraging to see data from long-term extension trials that can offer symptom relief and remission over time to those struggling with UC.”*
Through two years, the proportions of patients with adverse events (AEs), serious AEs, and serious infections in the ustekinumab groups were generally comparable to the placebo group. No new safety signals were observed.1 Ustekinumab has demonstrated a consistent safety profile in UC where trials show the treatment is well tolerated. In the primary randomised population of the Induction and Maintenance studies, a similar proportion of patients in the ustekinumab and placebo groups experienced AEs, serious AEs, infections and serious infections through to week 44. During the Induction phase, one death from an oesophageal varices haemorrhage was reported, and no malignancies, opportunistic infections or tuberculosis were reported. During the Maintenance phase, no deaths and two malignancies other than non‑melanoma skin cancer (NMSC) were reported (90 mg ustekinumab q8w: colon cancer [n=1]; 90 mg ustekinumab q12w: papillary renal cell carcinoma [n=1]). There was one patient-reported NMSC in the 90 mg ustekinumab q12w group (2 squamous cell carcinoma events).2,3
“The Phase 3 UNIFI two-year data builds upon the growing body of evidence of ustekinumab as a promising treatment option for UC, further underscoring our commitment to advancing research and development in inflammatory bowel diseases,” said Jan Wehkamp, M.D., Vice President, Gastroenterology Disease Area Leader, Janssen Research & Development, LLC. “We are proud to present these results for the first time at UEGW because we recognise the significant unmet needs that continue to persist in treating the life-altering symptoms of moderately to severely active UC.”
Janssen is presenting a total of 17 abstracts at this year’s UEGW congress, of which seven are oral presentations, including additional data from the UNIFI UC clinical trials programme. Another late-breaker on UNIFI data reports results from the maintenance study by individual ustekinumab IV induction dose and suggests an optimal regimen of IV induction and SC maintenance for the treatment of moderately to severely active UC (LB07).4 These data will also be delivered in an oral presentation today. Results from the UNITI Crohn’s disease (CD) clinical trial programme are also being presented at the congress.
Ustekinumab is currently approved for the treatment of adults with moderately to severely active ulcerative colitis in the European Union (EU) and the United States.5
# # #
*Prof Bruce Sands is a paid consultant for Janssen. He has not been compensated for any media work.
- Partial Mayo remission was defined as a partial Mayo score ≤2 points1
- Clinical remission was defined as a Mayo score ≤2 points, with no individual subscore >11
- Partial Mayo score includes stool frequency, rectal bleeding, and physician’s global assessment subscores and ranges from 0 to 96
- Symptomatic remission is defined as a stool frequency subscore of 0 or 1 and a rectal bleeding subscore of 01
About Ulcerative Colitis (UC)
UC affects up to 2.6 million people in Europe.7 It is a chronic disease of the large intestine, also known as the colon, in which the lining becomes inflamed and develops tiny open sores, or ulcers, that produce pus and mucous. UC is the result of an abnormal response by the body's immune system. Symptoms vary, but may include loose and more urgent bowel movements, persistent diarrhoea, abdominal pain, bloody stools, loss of appetite, weight loss and fatigue.8,9
About the UNIFI Programme
UNIFI is a Phase 3 study, designed to evaluate the safety and efficacy of ustekinumab induction and maintenance dosing for the treatment of moderately to severely active UC in adults who demonstrated an inadequate response to, or were unable to tolerate, conventional (i.e., corticosteroids, immunomodulators) or biologic (i.e., one or more tumour necrosis factor [TNF]-alpha antagonists and/or vedolizumab) therapies. Both the induction and maintenance studies are randomised, double blind, placebo-controlled, parallel group, multicentre studies. The induction study was conducted over a duration of at least 8 weeks for each participant. Participants achieving clinical response in the Induction study were eligible for the maintenance study. The maintenance study was 44 weeks in duration. The primary endpoint of the induction study was clinical remission at week 8, and the primary endpoint for the maintenance study was clinical remission at week 44 among responders to a single IV ustekinumab infusion. After completion of the maintenance study, a long-term extension study continues to follow two groups of eligible participants. The randomised population includes those participants who were in clinical response eight weeks after receiving single IV ustekinumab infusion and who were then randomised to receive ustekinumab 90 mg every 12 weeks (q12w) or ustekinumab 90 mg every 8 weeks (q8w) or placebo. Non-randomised patients include patients in clinical response following an IV and 90 mg SC ustekinumab dose who received SC ustekinumab 90 mg q8w and placebo responders who received SC placebo.2,3
About STELARA® (ustekinumab)
In the EU, ustekinumab is 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. Ustekinumab is also approved for the treatment of adult patients with moderately to severely active 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. Ustekinumab is approved for the treatment of moderate to severe plaque psoriasis in adults who failed to respond to, or who have a contraindication to, or are intolerant to other systemic therapies including ciclosporin, methotrexate (MTX) or psoralen plus ultraviolet A, and is also indicated for the treatment of moderate to severe plaque psoriasis in adolescent patients aged 12 years and older who are inadequately controlled by or are intolerant to other systemic therapies or phototherapies. In addition, 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.
The Janssen Pharmaceutical Companies of Johnson & Johnson maintain exclusive worldwide marketing rights to STELARA®.
Important safety information
Please refer to the full Summary of Product Characteristics for full prescribing information for ustekinumab:
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.
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.
# # #
1 Sands, B, et al. Efficacy and Safety of Ustekinumab for Ulcerative Colitis through 2 Years: UNIFI Long-Term Extension [Oral presentation for LB01] Presented at the 27th United European Gastroenterology Week (UEGW) congress 19−23 October 2019; Madrid, Spain
2 Sandborn WJ, et al. Efficacy and safety of ustekinumab as maintenance therapy in ulcerative colitis: Week 44 results from UNIFI [Abstract OP37]. Presented at the 14th Congress of the European Crohn’s and Colitis Organisation (ECCO), 6−8 March 2019; Copenhagen, Denmark.
3 Sands B, et al. Safety and efficacy of ustekinumab induction therapy in patients with moderate to severe ulcerative colitis: results from the Phase 3 UNIFI study [Abstract 54A]. Presented at the American College of Gastroenterology (ACG) Annual Scientific Meeting, 5−10 October 2018; Philadelphia, Pennsylvania.
4 Danese S, et al. Efficacy of Ustekinumab Subcutaneous Maintenance Treatment by Induction-Dose Subgroup in the UNIFI Study of Patients with Ulcerative Colitis [Abstract LB07]. Presented at the 27 United European Gastroenterology Week (UEGW) Congress, 19−23 October 2019; Madrid, Spain.
5 European Medicines Agency. 2019. https://www.medicines.org.uk/emc/product/4413/smpc (Accessed October 2019).
6 Van Assche G, et al. Sustained remission in patients with moderate to severe ulcerative colitis: results from the Phase 3 UNIFI maintenance study [Abstract: DOP47]. Presented at the 14 Congress of the European Crohn’s and Colitis Organisation (ECCO), 6−8 March 2019; Copenhagen, Denmark.
7 Ng SC, et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet 2017;390:2769–78.
8 Crohn's & Colitis UK. What is Ulcerative Colitis? Available at: https://www.crohnsandcolitis.org.uk/about-inflammatory-bowel-disease/ulcerative-colitis (Accessed October 2019).
9 Crohn’s & Colitis Foundation. ‘Living with Ulcerative Colitis’ leaflet. Available at: https://www.crohnscolitisfoundation.org/sites/default/files/legacy/assets/pdfs/living-with-ulcerative.pdf (Accessed October 2019)
Phone: +44 787-639-4360
(732) 524-2955 (office)
(732) 524-3922 (office)
About Business Wire
For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.
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
Sustainability Improvements Fail to Match Skyrocketing Air Travel Growth, According to OAG20.2.2020 12:00:00 EET | Press release
OAG, the world’s leading provider of travel data and insight, released a new report today – How Green is Your Airline? – that explores how the aviation industry is responding to growing momentum for sustainable and environmentally-friendly air travel. “Despite increased traveler interest in sustainability, the nature of the market makes driving real impact complex and difficult,” said John Grant, senior analyst with OAG. “Since 2000, the number of aircraft seats has grown at an average annual rate of 3.6 percent while available seat kilometers have increased 4.6 percent. Unfortunately, the positive changes made by airlines and regulators are being outweighed by increases to passenger growth.” OAG’s report provides an in-depth look at: Where current environmental measures, such as carbon offsetting, are falling short The complexities of reducing carbon impact in travel Market demand for sustainability and environmental data transparency Airlines, climate neutrality claims and greenwashi
Efficient Assistance, YITU AI Aids Epidemic Prevention and Control of COVID-19 Outbreak20.2.2020 11:59:00 EET | Press release
On February 4th, Shanghai Public Health Clinical Center, one of the authoritative institutions in the field of infectious diseases in China and the core unit for the treatment of COVID-19 in Shanghai, published the article “AI Aids the Scientific Prevention and Control, Intelligent Evaluation System of Chest CT for COVID-19 Launched in Shanghai Public Health Clinical Center” on its official WeChat platform. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20200220005333/en/ Pic 1: User interface of the Intelligent Evaluation System of Chest CT for COVID-19 (Photo: Business Wire) The article announced the latest results of its use of artificial intelligence technology to help doctors carry out intelligent quantitative analysis and evaluation of therapeutic effects of novel coronavirus lesions based on CT images. Since the outbreak of COVID-19, Yitu Healthcare responded quickly. The main R & D team sacrificed their vacations and f
Galderma Announces New England Journal of Medicine Publication from Phase 2 Study of Investigational Therapy Nemolizumab in Patients with Moderate to Severe Prurigo Nodularis20.2.2020 11:00:00 EET | Press release
Galderma today announced that The New England Journal of Medicine (NEJM) has published full results from the Phase 2 study of its investigational therapy nemolizumab in adult patients suffering from moderate-to-severe prurigo nodularis (PN). PN is a rare, potentially debilitating, chronic skin condition with thick skin nodules covering large body areas and associated severe pruritus. It frequently leads to a severe quality of life impairment. Nemolizumab is a first-in-class investigational monoclonal antibody that blocks signaling of IL-31 that play a key role in the pathogenesis of PN. Nemolizumab’s safety and efficacy have not been fully evaluated by any regulatory authority. In this study, 70 patients with moderate to severe PN and severe pruritus were randomized to receive subcutaneous nemolizumab 0.5 mg/kg every 4 Weeks from baseline to Week 8 or matching placebo injections (at weeks 0,4 and 8). Nemolizumab met the primary endpoint of a greater improvement in Peak Pruritus Numeric
SES Responds to Intelsat’s Ex-parte Submission to the FCC Regarding the C-Band Spectrum Clearing Process20.2.2020 10:58:00 EET | Press release
SES S.A. today notes the comments made by Intelsat in its ex-parte submission to the U.S. Federal Communication Commission (FCC) dated 19 February 2020. SES reaffirms its steadfast support for the Commission’s objectives to ensure global leadership in 5G, and it stands ready, willing, and able to play a central role in the expedited clearing of a portion of the C-band. SES believes that there remains an important role for the C-Band Alliance (CBA), and that the CBA’s collaborative clearing plan is the most efficient path to clear the spectrum. That said, SES is prepared to act on its own in the clearing process if necessary, while protecting its customers. SES is disappointed by Intelsat’s eleventh-hour attempt to renounce its commitments made to other CBA members and the Commission over the course of this proceeding, in aid of a transparent and egregious attempt to capture a greater share of the proposed accelerated relocation payments. Having worked collaboratively for a long period
BrandShield Launches ElectionShield Product to Protect Political Campaigns From Online Threats20.2.2020 10:00:00 EET | Press release
BrandShield, a leading provider of services from brand protection to online threat hunting, has today announced the launch of ElectionShield. Developed to protect political campaigns around the World from threats, such as fraudulent fundraising sites; phishing; social phishing; and impersonation, ElectionShield will be officially launched at one the World’s leading cybersecurity events, the RSA Conference in San Francisco, on February 24 - 28, 2020. BrandShield is exhibiting at South Expo, Booth# 3119. ElectionShield utilizes BrandShield’s market-leading technology to protect political campaigns and candidates from a growing range of online threats. These include social impersonation; fraudulent fundraising schemes; domain squatting; sale of unauthorized merchandise; fake social media content; phishing, social phishing and fake news. The last few years have seen a proliferation of fake social media content, in some cases using ‘deep fake’ video, designed to attack politicians. Accordin
Breath Therapeutics, a Zambon company, initiates BOSTON-3 and BOSTON-4, two additional clinical studies for the treatment of bronchiolitis obliterans syndrome (BOS)20.2.2020 09:00:00 EET | Press release
Zambon, a multinational pharmaceutical company that focuses on innovation and development with the aim to improve the quality of people’s health and patients’ lives, and Breath Therapeutics, a Zambon company, specializing in advanced inhaled therapeutics for severe respiratory diseases, announced today the initiation of the BOSTON-4 phase 2 multi-center clinical study of Liposomal Cyclosporine A for Inhalation (L‑CsA‑i) for the treatment of bronchiolitis obliterans syndrome (BOS) following allogeneic hematopoietic stem cell transplant (alloHSCT). Additionally, the BOSTON-3 open-label extension study has been initiated and is open to eligible participants who complete the BOSTON‑1 and ‑2 phase 3 studies currently underway to evaluate L‑CsA‑i for the treatment of BOS following lung transplantation. Anne Bergeron, MD, PhD, Prof, Hôpital Saint Louis, Paris said, “Bronchiolitis obliterans syndrome is the primary noninfectious pulmonary complication in patients who undergo allogeneic HSCT. D
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