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Novartis Data Show AIN457 Significantly Reduced Signs And Symptoms In Patients With Hard-To-Treat Moderate-To-Severe Plaque Psoriasis

AppId is over the quota AppId is over the quota Article adapted by Medical News Today from original press release. Click ‘references’ tab above for source.
Visit our eczema / psoriasis section for the latest news on this subject. 1. Paul C, Mroweitz U, Nakayama J et al. Secukinumab, a fully human, anti-interleukin (IL)-17A monoclonal antibody improves signs and symptoms of hand and foot psoriasis: results from a phase II regimen-finding trial. Presented at: 21st Congress of the European Academy of Dermatology and Venereology; 27-30 September, 2012; Prague, Czech Republic. Poster PRA12-0816.

2. Gaffen SL. Structure and signaling in the IL-17 receptor family. Nat Rev Immunol. 2009;9(8):556-67.


3. Ivanov S, Linden A. Interleukin-17 as a drug target in human disease. Trends Pharmacol Sci. 2009;30(2):95-103.


4. Kopf M, Bachmann MF, Marsland BJ. Averting inflammation by targeting the cytokine environment. Nat Rev Drug Discov. 2010;9(9):703-18.


5. Radtke MA, Langenbruch AK, Schafer I et al. Nail psoriasis as a severity indicator: results from the PsoReal study. Patient Relat Outcome Meas. http://www.eczemablog.net/ 2011;2:1-6


6. Pettey AA, Balkrishnan R, Rapp et al. Patients with palmoplantar psoriasis have more physical disability and discomfort than patients with other forms of psoriasis: implications for clinical practice. J Am Acad Dermatol. 2003;49(2) :271-275.


7. Gottlieb AB, Reich K, Philipp S et al. Secukinumab improves signs and symptoms of nail psoriasis: results from a phase II regimen-finding trial. Presented at: 21st Congress of the European Academy of Dermatology and Venereology; 27-30 September, 2012; Prague, Czech Republic. Poster PRA12-0668.


8. Wilsmann-Theis D, Terui T, Draelos Z et al. Improvement with secukinumab on patient reported skin related quality of life (QoL) and health status among moderate-to-severe plaque psoriasis patients: results from a phase II regimen-finding trial. Presented at: 21st Congress of the European Academy of Dermatology and Venereology; 27-30 September, 2012; Prague, Czech Republic. Poster: PRA12-0822.


9. Rapp SR, Feldman SR, Exum, ML et al. Psoriasis causes as much disability as other major medical diseases. J Am Acad Dermatol. 1999;41(3):401-407.Leipe J, Grunke M, Dechant C et al. Role of Th17 cells in human autoimmune arthritis. Arthritis Rheum. 2010;62:2876-2885.


10. Rich P.A. et al. Secukinumab, a new fully human monoclonal anti-Interleukin-17A antibody, in the treatment of moderate-to-severe plaque psoriasis: Interim efficacy and safety data from a phase II regimen-finding trial. Presented at: 20th Congress of the European Academy of Dermatology and Venereology; 20-24 October, 2011; Lisbon, Portugal. Oral presentation FC01.6.


11. Genovese M, Kellner H, Durez P, et al. Secukinumab treatment improves ACR50, HAQ-DI and EULAR remission rates in patients with rheumatoid arthritis. At: EULAR 2012, The Annual European Congress of Rheumatology; 6-9 June 2012, Berlin, Germany. Abstract 2925.


12. Baeten D, Sieper J, Emery P, et al. The anti-il17a monoclonal antibody secukinumab (AIN457) showed good safety and efficacy in the treatment of active ankylosing spondylitis. At: EULAR 2011, The Annual European Congress of Rheumatology, 25-28 May 2011, London, UK. Abstract 0174.


13. McInnes I, Sieper J, Braun J, et al. Anti-Interleukin 17A monoclonal antibody secukinumab reduces signs and symptoms of psoriatic arthritis in a 24-week multicenter, double-blind, randomized, placebo- controlled trial. Presented at: Annual Scientific Meeting of the American College of Rheumatology/Association of Rheumatology Health Professionals; 4-9 November 2011; Chicago, IL. Abstract 19541.


14. Raychaudhuri SP, Farber EM. The prevalence of psoriasis in the world. J Eur Acad Dermatol Venereol. 2001;15:16–17.


15. Nestle FO, Kaplan DH, Barker J. Psoriasis. N Engl J Med 2009;361:496-509.


16. Herrier R. Advances in the treatment of moderate-to-severe plaque psoriasis. Am J Health-Syst Pharm 2011;68:795-806.


17. Farley E, Masrour S, McKey J et al. Palmoplantar psoriasis: a phenotypical and clinical review with introduction of a new quality-of-life assessment tool. J Am Acad Dermatol. 2009;60(6):1024-1031.


Disclaimer


The foregoing release contains forward-looking statements that can be identified by terminology such as “promising,” “on track,” “expected,” “encouraging,” “may,” “look forward to,” “to follow,” or similar expressions, or by express or implied discussions regarding potential marketing submissions or approvals for AIN457, or the timing of any such submissions or approvals, or regarding potential future revenues from AIN457. You should not place undue reliance on these statements. Such forward-looking statements reflect the current views of management regarding future events, and involve known and unknown risks, uncertainties and other factors that may cause actual results with AIN457 to be materially different from any future results, performance or achievements expressed or implied by such statements. There can be no guarantee that AIN457 will be submitted or approved for approval in any market, or at any particular time. Nor can there be any guarantee that AIN457 will achieve any particular levels of revenue in the future. In particular, management’s expectations regarding AIN457 could be affected by, among other things, unexpected clinical trial results, including unexpected new clinical data and unexpected additional analysis of existing clinical data; unexpected regulatory actions or delays or government regulation generally; competition in general; government, industry and general public pricing pressures; the company’s ability to obtain or maintain patent or other proprietary intellectual property protection; unexpected manufacturing issues; the impact that the foregoing factors could have on the values attributed to the Novartis Group’s assets and liabilities as recorded in the Group’s consolidated balance sheet, and other risks and factors referred to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those anticipated, believed, estimated or expected. Novartis is providing the information in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this press release as a result of new information, future events or otherwise.

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UK, Burson-Marsteller. “Novartis Data Show AIN457 Significantly Reduced Signs And Symptoms In Patients With Hard-To-Treat Moderate-To-Severe Plaque Psoriasis.” Medical News Today. MediLexicon, Intl., 1 Oct. 2012. Web.
7 Apr. 2013. APA

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New Data Demonstrate Stelara® (Ustekinumab) Is Effective, Well-Tolerated And Improved QOL In Patients With Moderate To Severe Plaque Psoriasis

AppId is over the quota AppId is over the quota Article adapted by Medical News Today from original press release. Click ‘references’ tab above for source.
Visit our eczema / psoriasis section for the latest news on this subject. Study Design and Results

TRANSIT study
Design: A 52 week, open-label, Phase 4 study of 489 patients designed to compare two methods of transitioning patients from methotrexate to ustekinumab. The first was discontinuation of methotrexate with immediate initiation of ustekinumab and the second was initiation of ustekinumab with overlap and gradual dose reduction of methotrexate over four weeks. Results: Ustekinumab was well tolerated, with 8% of patients in each transition arm experiencing a serious adverse event (AE), and associated with sustained efficacy;http://www.eczemablog.net/  76% and 77% of patients, in the methotrexate immediate cessation arm and the methotrexate gradual withdrawal arm respectively, achieved at least a 75% improvement from baseline in their Psoriasis Area and Severity Index score (PASI 75) at Week 52. The data showed there was no difference in terms of the number and types of AE or efficacy outcomes, whether given ustekinumab after immediate cessation of methotrexate or if methotrexate is gradually withdrawn over 4 weeks.1


PHOENIX 2
Design: 1,230 patients with moderate-to-severe plaque psoriasis were randomised to receive ustekinumab 45 mg or 90 mg at weeks 0, 4 and every 12 weeks thereafter, or placebo at weeks 0 and 4. Patients initially randomised to placebo at baseline were assigned to cross over to either ustekinumab 45 mg or 90 mg at weeks 12, 16 and every 12 weeks thereafter. Investigators were permitted to adjust ustekinumab dosing based on clinical judgment after Week 52 of the study.* Results: With up to five years of ustekinumab treatment, high levels of clinical responses were achieved and maintained in the overall population; 76.5% and 78.6% of patients who received STELARA 45 mg and 90 mg, respectively, achieved a PASI 75 response at the end of the treatment period. The safety profile of ustekinumab was generally comparable between patients who received 45 mg or 90 mg, with or without dose adjustments.3


*PHOENIX 2 study design involved a revised dosing schedule for partial responders which is not included in the approved EMA Summary of Product Characteristics for STELARAR.


Clinical Trial Safety Database Analysis


Design: Safety data were pooled from four ustekinumab psoriasis studies (one Phase 2 and three Phase 3 [PHOENIX 1, PHOENIX 2, and ACCEPT]) in which patients were treated for up to five years. Rates of overall and targeted adverse events were analysed by ustekinumab dose received (45 mg or 90 mg) and by year of follow-up (Year 1 to 5) to evaluate potential dose-response or impact of increasing duration of exposure.
Results: Analyses included 3,117 patients with a total of 8.998 PY of follow-up. Rates of safety events were generally comparable between patients who received 45 mg and 90 mg; and generally consistent over time from Year 1 through 5. The overall safety profile of ustekinumab remained stable in adults with moderate-to-severe plaque psoriasis receiving up to five years of ustekinumab treatment. No effect of dose and no effect of increasing duration of exposure were observed.4


PSOLAR
Design: A disease-based registry study that captures multiple forms of psoriasis therapy that is planned to enroll approximately 12,000 patients. In August 2011, 9,495 patients were available in the last annual data extract reflecting 13,733 PY of exposure. Patients that are eligible for systemic therapies, including ustekinumab and infliximab, are enrolled and followed biannually.
Results: Preliminary findings on rates of infection, malignancy (excluding non-melanoma skin cancers) and major adverse cardiovascular events (MACE) observed since the registry opened in 2007 were reported.5-7 In patients exposed to ustekinumab and infliximab, no new safety signals for malignancy, MACE or infection were identified in patients undergoing actual clinical use in more than 250 centres internationally.5-7


About Psoriasis


Psoriasis is a chronic disease caused when the immune system mistakenly attacks healthy skin cells, speeding up skin cell production.10 Plaque psoriasis, the most common type of psoriasis,11 often results in patches of thick, red or inflamed skin covered with silvery scales (known as plaques). These plaques usually itch or feel sore, can crack and bleed, and can occur anywhere on the body.


Psoriasis affects 125 million people worldwide and around 11 million people in Europe.12,13 The type, symptoms and severity of psoriasis may differ from one person to another, with its effects ranging from mild or moderate, to severe. Nearly one-quarter of people with psoriasis have cases that are considered moderate to severe.14


Biological therapies represent an advancement in the treatment of moderate to severe plaque psoriasis. Long-term data on available treatment options is important to support healthcare professionals in their decision-making about the most appropriate treatment option for patients.


For more information about psoriasis, available treatment options and tools to assess the medical severity of psoriasis please visit http://www.psoriasis360.com


About STELARA (Ustekinumab)


Ustekinumab is indicated 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 and PUVA (psoralen plus UVA).15


The recommended dosing regimen for ustekinumab is an initial dose of 45 mg administered subcutaneously, followed by a 45 mg dose 4 weeks later, and then every 12 weeks thereafter. For patients with a body weight of greater than 100 kg the recommended dose is 90 mg administered subcutaneously, followed by a 90 mg dose 4 weeks later, then every 12 weeks thereafter. (In these patients, 45 mg was also shown to be efficacious. However, 90 mg resulted in greater efficacy). Consideration should be given to discontinuing treatment in patients who have shown no response up to 28 weeks of treatment.15 Ustekinumab is the only subcutaneous treatment for psoriasis available with every 12-week (quarterly) dosing, or as few as four injections per year, following two initial doses.15-17


STELARA is not recommended for use in children and adolescents below age 18 due to a lack of data on safety and efficacy.


Janssen Biotech, Inc. discovered and developed ustekinumab and has exclusive marketing rights to the product in the United States. Janssen pharmaceutical companies have exclusive marketing rights in all countries outside of the United States.


Important Safety Information14


Ustekinumab is a selective immunosuppressant and may have the potential to increase the risk of infections and reactivate latent infections. Serious infections have been observed in patients receiving ustekinumab in clinical trials. Do not start ustekinumab during an active infection. If a serious infection develops, monitor patients carefully and stop ustekinumab until the infection resolves. Patients should be evaluated for tuberculosis (TB) infection prior to initiating treatment with ustekinumab.


Ustekinumab is a selective immunosuppressant. Immunosuppressive agents have the potential to increase the risk of malignancy. Malignancies have been observed in patients receiving ustekinumab in clinical trials.


Caution should be exercised when considering the use of ustekinumab in patients with a history of malignancy or when considering continuing treatment in patients who develop a malignancy.


Serious allergic reactions have been reported in the post-marketing setting, in some cases several days after treatment. Anaphylaxis and angioedema have occurred. If an anaphylactic or other serious allergic reaction occurs, administration of ustekinumab should be discontinued immediately and appropriate treatment instituted.


It is recommended that live viral or live bacterial vaccines (such as Bacillus of Calmette and Guerin [BCG]) should not be given concurrently with STELARA.


No overall differences in efficacy or safety in patients age 65 and older who received STELARA were observed compared to younger patients. Because there is a higher incidence of infections in the elderly population in general, caution should be used in treating the elderly.


Special Warnings and Precautions for Use14


Concomitant immunosuppressive therapy: Caution should be exercised when considering concomitant use of other immunosuppressants and ustekinumab or when transitioning from other immunosuppressive biologics.


References


1. Paul C et al. Long-term safety and efficacy of ustekinumab in patients with psoriasis inadequately responding to methotrexate: Week 52 TRANSIT results. Presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Oral session FC02.1.


2. Reich K et al. Long-term improvement in patient-reported outcomes after transition from methotrexate to ustekinumab in moderate to severe psoriasis: TRANSIT Week 52 results. Poster presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Poster 955.


3. Langley R et al. Long term efficacy and safety of ustekinumab in patients with moderate to severe psoriasis through 5 years of follow-up: results from the PHOENIX 2 long-term extension. Poster presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Poster 976.


4. Papp K et al. Long term safety of ustekinumab in patients with moderate to severe psoriasis through up to 5 years of continuous follow-up. Poster presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Poster 965.


5. Naldi L et al. Major adverse cardiovascular events in the Psoriasis Longitudinal Assessment and Registry (PSOLAR) study: current status of observations. Presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Oral session FC02.7.


6. Leonardi C et al. Serious infection events in the Psoriasis Longitudinal Assessment and Registry (PSOLAR) study: current status of observations. Poster presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Poster 977.


7. Langley R et al. Malignancy events in the Psoriasis Longitudinal Assessment and Registry (PSOLAR) study: current dtatus of observations. Poster presented at the 21st European Association of Dermatology & Venereology (EADV) congress, Prague 27–30 September 2012. Poster 973.


8. National Psoriasis Foundation. Related Health concerns: Psoriasis comorbidities. Available at: http://www.psoriasis.org/about-psoriasis/related-conditions. Last accessed September 2012


9. Augustin M et al. A framework for improving the quality of care for people with psoriasis. JEADV 2012; 26 (Supplement 4):1–16.


10. The Psoriasis Association. Available at: http://www.psoriasis-association.org.uk/pages/view/about-psoriasis. Last accessed September 2012.


11. National Psoriasis Foundation. Psoriasis types. Available at: http://www.psoriasis.org/about-psoriasis/types. Last accessed September 2012.


12. National Psoriasis Foundation. About Psoriasis: Statistics. Available at: http://www.psoriasis.org/about/stats. Last accessed September 2012.


13. Lecluse LL et al. National registries of systemic treatment for psoriasis and the European ‘Psonet’ initiative. Dermatology. 2009;218 (4):347-56.


14. Ustekinumab European Summary of Product Characteristics. Date: March 2012.


15. Wyeth Pharmaceuticals. Enbrel Summary of Product Characteristics.


16. Abbott Laboratories Ltd. Humira Summary of Product Characteristics.


17. Schering-Plough Ltd. Remicade Summary of Product Characteristics.


To view a film of experts discussing the data, please visit:
http://www.brainshark.com/janssencns/PsoriasisInterviews


Janssen

Please use one of the following formats to cite this article in your essay, paper or report:

MLA

Janssen. “New Data Demonstrate StelaraR (Ustekinumab) Is Effective, Well-Tolerated And Improved QOL In Patients With Moderate To Severe Plaque Psoriasis.” Medical News Today. MediLexicon, Intl., 2 Oct. 2012. Web.
7 Apr. 2013. APA
Janssen. (2012, October 2). “New Data Demonstrate StelaraR (Ustekinumab) Is Effective, Well-Tolerated And Improved QOL In Patients With Moderate To Severe Plaque Psoriasis.” Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/250915.php.

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