Member News
May 22, 2024
Novartis Pharmaceuticals Canada Inc.
- Approval is based on the two largest Phase III trials conducted in HS – SUNSHINE and SUNRISE – demonstrating the safety and efficacy of Cosentyx®in HS1
- HS is a chronic, immunological, inflammatory skin condition estimated to affect 1 in 100 people worldwide causing painful, boil-like lumps that can lead to open wounds and irreversible scarring2,3,4
- The new treatment for HS reinforces Novartis’ commitment to delivering new, innovative therapies that improve health outcomes for patients inCanada
MONTRÉAL, QC–Novartis Pharmaceuticals Canada Inc. (Novartis) is pleased to announce that Health Canada has granted Cosentyx®(secukinumab) with a Notice of Compliance (NOC) for the treatment of adult patients with moderate to severe hidradenitis suppurativa (HS)(acne inversa) who have responded inadequately to conventional systemic hidradenitis suppurativa therapy – representing a safe and efficacious new treatment option for Canadians living with the condition.1
While the exact cause and prevalence of HS is unknown,2it is estimated to affect 1-4 per cent of the Canadian population4which equates to between 300,000 and 1 million people.5HS is considered a chronic and progressive disease, meaning it can worsen over time and have a significant impact on a patient’s everyday life.4
“People living with HS often suffer physically and mentally from the effects of the condition,” saidLatoya Palmer, Founder of Hidradenitis and Me Support Group. “Ensuring there are a wide range of treatment options is vital for each individual to find the right path for them.”
The safety and efficacy of Cosentyx®was assessed in the two largest Phase III trials ever conducted in HS – SUNSHINE (M2301) and SUNRISE (M2302). The global, multicentre,randomized, double-blind, placebo-controlled clinical trials studied1,084 adult patients with moderate to severe HS.1
“Patients who have been diagnosed with advanced HS often have limited treatment options available to them,” said Dr.Susan Poelman, Dermatologist and President of the HS Foundation inCanada. “The approval of a new treatment option for HS is a welcome new addition for people living with the condition and will bring hope to patients that have achieved suboptimal control with current available therapies.”
In addition to HS, Cosentyx®has been previously approved for use inCanadafor a variety of conditions including plaque psoriasis, psoriatic arthritis, axial spondyloarthritis and juvenile idiopathic arthritis.1Given its well-known and proven safety profile, Cosentyx®will provide physicians and their patients with more treatment options to decide on the most appropriate course of action to treat their HS.
“This approval will offer a new treatment option for patients currently living with HS,” added Dr.Mark Kirchhof, Division Head of Dermatology in the Faculty of Medicine at theUniversity of Ottawaand The Ottawa Hospital. “Cosentyx®will provide dermatologists with a familiar treatment for this complex condition.”
“More than 1 million patients have been treated with Cosentyx®worldwide since its launch in 2015, and we are proud that is now available inCanadaas a much-needed treatment to those suffering with HS,” saidMark Vineis, Country President Novartis Pharmaceuticals Canada Inc. “This approval is another example of Novartis’ commitment to bringing innovative medicines to improve patient outcomes inCanada.”
About NovartisNovartis is a focused innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. Reimagine medicine with us: Visit us athttps://www.novartis.comand connect with us onLinkedIn,Facebook,X/TwitterandInstagram.
InCanada, Novartis Pharmaceuticals Canada Inc. employs approximately 600 people to serve the evolving needs of patients and the healthcare system, and invests over$30 millionin R&D yearly in the country. For more information visitwww.novartis.ca.
About the SUNSHINE and SUNRISE trials6,7,8The SUNSHINE (NCT03713619) and SUNRISE (NCT03713632) trials comprise the largest Phase III program in hidradenitis suppurativa (HS), with a combined enrollment of more than 1,000 patients in 40 countries. SUNSHINE and SUNRISE evaluated the short- (16 weeks) and long-term (up to 52 weeks) efficacy, safety and tolerability of two dose regimens of Cosentyx®(secukinumab) in adults with moderate to severe HS.
About Cosentyx®(secukinumab)
Cosentyx®is the first and only fully human biologic that directly inhibits interleukin-17A, an important cytokine involved in the inflammation of psoriatic arthritis (PsA), moderate to severe plaque psoriasis, ankylosing spondylitis (AS) and non-radiographic axial spondyloarthritis (nr-axSpA).9,10Cosentyx®is a proven medicine and has been studied clinically for more than 14 years. The medicine is backed by robust evidence, including 5years of clinical data in adults supporting long-term safety and efficacy across moderate to severe plaque psoriasis, PsA and AS.11,12,13,14,15,16,17These data strengthen the position of Cosentyx®as a treatment across AS, nr-axSpA, PsA, moderate to severe plaque psoriasis (adult and pediatric) and two subtypes of juvenile idiopathic arthritis (JIA), enthesitis-related arthritis and juvenile psoriatic arthritis.9More than 1 million patients have been treated with Cosentyx®worldwide since its launch in 2015.
Media Contact:
Karla Fuentes Arellano
Communications & Engagement Lead
E-mail:camlph.communications@novartis.com
M +1 514 633 7873
426329E
References
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1Cosentyx®Product Monograph. May 21, 2024. |
2NHS. Hidradenitis Suppurativa (HS). Accessed on March 2, 2024. Available at:https://www.nhs.uk/conditions/hidradenitis-suppurativa/. |
3American Academy of Dermatology. Hidradenitis Suppurativa: Overview. Accessed on March 2, 2024. Available at:https://www.aad.org/public/diseases/a-z/hidradenitis-suppurativa-overview#:~:text=Hidradenitis%20suppurativa%20(HS)%20is%20a,and%20treatment%20of%20this%20condition. |
4HS Heros. What is HS? Accessed on March 2, 2024. Available at:https://hsheroes.ca/what-is-hs/. |
5Canadian Dermatology Association. Hidradenitis Suppurativa. Accessed on March 2, 2024. Available at:https://dermatology.ca/public-patients/skin/hidradenitis-suppurativa/#:~:text=Fifty%20to%20300%20million%20people,people%20in%20Canada%20 |
have%20HS.&text=Hidradenitis%20suppurativa%20(HS)%20is%20a%20chronic%2C%20painful%20skin%20condition,hair%20follicles%20in%20the%20skin. |
6Kimball AB, Jemec GBE, Alavi A, et al. Secukinumab in moderate to severe hidradenitis suppurativa (SUNSHINE and SUNRISE): week 16 and 52 results of two identical, double-blind, placebo-controlled, phase 3 randomised trials. Lancet 2023; published online Feb 3. Accessed on March 2, 2024. Available at:https://doi.org/10.1016/S0140-6736(23)00022-3. |
7ClinicalTrials.gov. Study of Efficacy and Safety of Two Secukinumab Dose Regimens in Subjects With Moderate to Severe Hidradenitis Suppurativa (HS) (SUNRISE). NCT03713632. Accessed on March 2, 2024. Available at:https://clinicaltrials.gov/ct2/show/NCT03713632. |
8ClinicalTrials.gov. This is a Study of Efficacy and Safety of Two Secukinumab Dose Regimens in Subjects With Moderate to Severe Hidradenitis Suppurativa (HS). (SUNSHINE). NCT03713619. Accessed on March 2, 2024. Available at:https://clinicaltrials.gov/ct2/show/NCT03713619. |
9Novartis Europharm Limited. Cosentyx®(secukinumab): Summary of Product Characteristics. Accessed on March 2, 2024. Available at:https://www.ema.europa.eu/en/documents/product-information/cosentyx-epar-product-information_en.pdf. |
10Girolomoni G, Mrowietz U and Paul C. Psoriasis: rationale for targeting interleukin-17. Br J Dermatol 2012; 167: 717-724. Accessed on March 2, 2024. Available at:https://pubmed.ncbi.nlm.nih.gov/22716185/. |
11Baraliakos X, Braun J, Deodhar A, et al. Long-term efficacy and safety of secukinumab 150 mg in ankylosing spondylitis: 5-year results from the phase III MEASURE 1 extension study. RMD Open 2019; 5: e001005. |
12Bissonnette R, Luger T, Thaçi D, et al. Secukinumab demonstrates high sustained efficacy and a favourable safety profile in patients with moderate-to-severe psoriasis through 5 years of treatment (SCULPTURE Extension Study). J Eur Acad Dermatol Venereol 2018; 32: 1507-1514. |
13Mease PJ, Kavanaugh A, Reimold A, et al. Secukinumab Provides Sustained Improvements in the Signs and Symptoms of Psoriatic Arthritis: Final 5-year Results from the Phase 3 FUTURE 1 Study. ACR Open Rheumatol 2020; 2: 18-25. |
14Data on file. CAIN457F2310 (MEASURE 1 and 2): Pooled Safety Data. Novartis Pharmaceuticals Corp; July 23, 2018. |
15Data on file. CAIN457F2310 and CAIN457F2305 summary of 5-year clinical safety in (ankylosing spondylitis). Novartis Pharmaceuticals Corp; May 2019. |
16Data on file. CAIN457F2312 (FUTURE 2): 5 year-interim report. Novartis Pharmaceuticals Corp; May 2019. |
17McInnes IB, Mease PJ, Kirkham B, et al. Secukinumab, a human anti-interleukin-17A monoclonal antibody, in patients with psoriatic arthritis (FUTURE 2): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet 2015; 386: 1137-1146. |
Original source here.
