Le Lézard
Classified in: Health
Subjects: PDT, EGV, TRI

European Commission Approves TREMFYA® (guselkumab) for the Treatment of Moderate to Severe Plaque Psoriasis in the European Union


BEERSE, Belgium, November 23, 2017 /PRNewswire/ --

FOR MEDICAL AND TRADE MEDIA ONLY  

Janssen's guselkumab is the first biologic to be approved that selectively blocks interleukin (IL)-23   

Janssen-Cilag International NV announced today that the European Commission (EC) has approved TREMFYA® (guselkumab) for the treatment of adults with moderate to severe plaque psoriasis who are candidates for systemic therapy.[1] Guselkumab is the first biologic that selectively blocks interleukin (IL)-23, a key driver of the immune inflammatory response in psoriasis.[2],[3],[4],[5]

"We are delighted guselkumab will now be available to patients in Europe," said Kris Sterkens, Company Group Chairman, Janssen Europe, Middle East and Africa (EMEA). "With 14 million people in the region affected by this often painful and potentially disabling disease, we must continue the fight to help improve the lives of those affected. We are proud to be introducing an innovative new option to help address the continued needs of people living with plaque psoriasis."

Guselkumab is a self-injectable (following training) treatment for psoriasis. Treatment requires two starter doses, one initially and the other four weeks later, followed by a maintenance dose once every eight weeks (q8w) thereafter.[3],[4]

The EC approval is based on data from three Phase III clinical studies. The VOYAGE 1 and 2 trials, which compared guselkumab with placebo and HUMIRA® (adalimumab), showed high levels of skin clearance after just 16 weeks, with at least a 90% reduction in Psoriasis Area and Severity Index score (PASI 90) in 73.3% and 70.0% of patients receiving guselkumab, compared with 49.7% and 46.8% in patients receiving adalimumab, respectively (P<0.001).[2],[3]   

The NAVIGATE trial evaluated patients who did not achieve a response of cleared or minimal disease (Investigator's Global Assessment [IGA] score of 0 or 1) by week 16 when treated with STELARA® (ustekinumab), and were then randomised to either switch to guselkumab or continue on ustekinumab.[4] The guselkumab group benefited significantly from the switch, with a significantly higher mean number of visits at which patients achieved an IGA score of 0 or 1 and at least a 2-grade improvement from week 28 through week 40 (relative to week 16), compared to the ustekinumab group (1.5 vs 0.7; P<0.001).[4]

During the clinical development programme for guselkumab in psoriasis there were no clear signals of increased risk of malignancy, major cardiovascular events or serious infections, including tuberculosis and the re-activation of latent tuberculosis.[2],[3],[4] Adverse events reported in at least 5% of guselkumab-treated patients during the first 16 weeks in the VOYAGE 1 and 2 trials included: nasopharyngitis, upper respiratory tract infection, injection site erythema, headache, arthralgia, pruritus and back pain. The types of adverse events reported remained generally consistent through 48 weeks of treatment.[2],[3]

Marketing authorisation follows a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), issued on 14 September 2017.[6] This approval allows for the marketing of TREMFYA® (guselkumab) in all 28 member states of the European Union as well as the European Economic Area countries (Norway, Iceland and Liechtenstein). Janssen received US FDA approval of guselkumab for the treatment of adults with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy in July 2017.[7]

Information for Editors  

About guselkumab  

VOYAGE 1, VOYAGE 2 and NAVIGATE studies   


Lifecycle development  

Phase III studies are being undertaken to evaluate the efficacy and safety of guselkumab for patients with psoriatic arthritis.[9] A Phase III comparator study (the ECLIPSE study) is underway to evaluate the efficacy of guselkumab versus Cosentyx® (secukinumab), an IL-17A inhibitor, in patients with moderate to severe plaque psoriasis.[10]

TREMFYA® and STELARA® are registered trademarks of Janssen Biotech, Inc. HUMIRA® is a registered trademark of AbbVie Inc. COSENTYX® is a registered trademark of Novartis AG.

About Psoriasis   

What it is  

The most common form of psoriasis is plaque psoriasis, usually resulting in areas of thick, red or inflamed skin covered with silvery scales which are known as plaques.[11] The inconsistent nature of psoriasis means that even when plaques appear to subside, many patients still live in fear of their return.[12]

Impact  

Psoriasis can cause great physical and psychological burden. A study comparing psoriasis to other prominent conditions found its mental and physical impact comparable to that seen in cancer, heart disease and depression.[13]

Psoriasis is also associated with several comorbidities including psoriatic arthritis, cardiovascular diseases, metabolic syndrome, chronic obstructive pulmonary disorder (COPD) and osteoporosis.[14],[15]

In addition, many individuals are faced with social exclusion, discrimination, and stigma because of their disease.[16]

About the Janssen Pharmaceutical Companies of Johnson & Johnson   

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at http://www.janssen.com/emea. Follow us on Twitter: @JanssenEMEA.

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 Europe of guselkumab. 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 or Johnson & Johnson. Risks and uncertainties include, but are not limited to: challenges inherent in product research and development, including uncertainty of clinical success and obtaining regulatory approvals; uncertainty of commercial success; competition, including technological advances, new products and patents attained by competitors; challenges to patents; 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 January 1, 2017, including under "Item 1A. Risk Factors," its most recently filed Quarterly Report on Form 10-Q, including under the caption "Cautionary Note Regarding Forward-Looking Statements," and the company's subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at http://www.sec.gov/, http://www.jnj.com/ or on request from Johnson & Johnson. Neither 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. European Commission: Tremfya (guselkumab). Available at: http://ec.europa.eu/health/documents/community-register/html/h1234.htm. Accessed: November 2017.

2. Blauvelt A and Papp K.A et al. J Am Acad Dermatol 2017;76(3):405-17. 

3. Reich K and Armstrong A.W et al. J Am Acad Dermatol 2017;76(3):418-31. 

4. Langley R.G and Tsai T.F et al. Br J Dermatol 2017 [Epub ahead of print]. 

5. Bachelez H. The Lancet 2017;390:208-10. 

6. European Medicines Agency. 2017. Available at: http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/004271/smops/Positive/human_smop_001193.jsp&mid=WC0b01ac058001d127&source=homeMedSearch&category=human. Accessed November 2017. 

7. US Food and Drug Administration. 2017. Available at: https://www.fda.gov/drugs/developmentapprovalprocess/druginnovation/ucm537040.htm . Accessed November 2017. 

8. Griffiths C.E and Papp K.A et al. 26th European Academy of Dermatology and Venereology Congress (EADV 2017) 13-17 Sept, 2017; Geneva, Switzerland;D3T01.1I. 

9. ClinicalTrials.gov. Available at: clinicaltrials.gov/ct2/show/NCT03158285. Accessed November 2017. 

10. ClinicalTrials.gov. Available at: clinicaltrials.gov/ct2/show/NCT03090100. Accessed November 2017. 

11. National Institute of Arthritis and Musculoskeletal and Skin Disorders. NIH Medline Plus 2003;12(1):20-1. 

12. US Food and Drug Administration. 2016. Available at: https://www.fda.gov/downloads/ForIndustry/UserFees/PrescriptionDrugUserFee/UCM529856.pdf .  Accessed November 2017. 

13. Rapp S.R and Feldman S.R et al. J Am Acad Dermatol 1999;41(3):401-7. 

14. Nijsten T and Wakkee M J Invest Dermatol 2009;129(7):1601-3. 

15. National Psoriasis Foundation. Available at: psoriasis.org/about-psoriasis/related-conditions. Accessed November 2017. 

16. World Health Organization. 2016. Available at: apps.who.int/iris/bitstream/10665/204417/1/9789241565189_eng.pdf. Accessed November 2017. 

Job code: [PHEM/IMM/1017/0004]. Date of preparation: November 2017.



These press releases may also interest you

at 00:25
Shanghai Junshi Biosciences Co., Ltd ("Junshi Biosciences," HKEX: 1877; SSE: 688180), a leading innovation-driven biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies, announced its financial...

28 mar 2024
The report titled "Central Lab Market by Service Type (Anatomic Pathology/Histology, Biomarker Services, Genetic Services), Phase (Phase 1, Phase 2, Phase 3), Therapeutic Area, End-use - Global Forecast 2024-2030" is now available on...

28 mar 2024
The report titled "Personalized Nutrition Market by Measurement Type (Active Measurement, Standard Measurement), Application (Indication-based, Standard Supplements), Distribution Channel, End-Use - Global Forecast 2024-2030" is now available on...

28 mar 2024
The report titled "Carbon Dioxide Incubator Market by Product (Air Jacketed CO2 Incubators, Direct Heat CO2 Incubators, Water Jacketed CO2 Incubators), Capacity (100-200 Litre, Above 200 Litre, Below 100 Litre), Application, End User - Global...

28 mar 2024
The "Global Clinical In Vitro Diagnostic Medical Laboratory Services Market: Strategy & Trends with Volume & Price Forecasts by Chemistry, Hematology, Microbiology, Pathology, Covid-19, and Molecular Dx by Country. Updated with Impact of COVID-19"...

28 mar 2024
The "Molecular Diagnostics at the Point of Care. By Application, Technology, Place, Product and by Country. With Executive Guides and Customization 2023 - 2027 " report has been added to  ResearchAndMarkets.com's offering. Infectious disease Dx is...



News published on and distributed by: