Novartis publicerar studien PARADIGM på barn och ungdomar med MS i NEJM

Novartis publicerar studie på barn och ungdomar med MS i NEJM
Novartis meddelade idag att TheNew England Journal of Medicine (NEJM)har publicerat resultatet från Fas III studien PARADIGM,  på Gilenya (fingolimod). Den första randomiserade studien speciellt designad för barn och ungdomar (10-17 år) med RMS.

 

Novartis today announced that TheNew England Journal of Medicine (NEJM) has published full results from the landmark Phase III Gilenya® (fingolimod) PARADIGMS study, the first-ever controlled, randomized study specifically designed for children and adolescents (aged 10 to 17) with relapsing forms of MS (RMS). Children and adolescents with MS experience more frequent and often more severe relapses than those seen in adults with MS[1]. The negative effect of relapses on movement, memory and thinking prevents patients from enjoying their childhood and adolescent years to the full, often leaving them feeling isolated and anxious[2]. PARADIGMS met the primary endpoint of significantly reducing the rate of relapses when compared to interferon beta-1a intramuscular injections over a period of up to two years[3]. The study also met several secondary clinical and imaging endpoints[3].

”I’d like to thank all the children who participated in the PARADIGMS study, and their families, who have helped transform the outlook for pediatric patients living with relapsing MS,” said Dr. Tanuja Chitnis, Principle Investigator for PARADIGMS and Director of the Partners Pediatric Multiple Sclerosis Center, Massachusetts General Hospital, Boston, US, and Scientist, Ann Romney Center, Brigham and Women’s Hospital, Boston, US. ”These data, published today, will go a long way in helping to advance knowledge and understanding amongst the MS community of how to evaluate and treat pediatric patients with MS.”

Results from PARADIGMS show that, compared to interferon beta-1a, Gilenya[3]:

  • Significantly reduced relapse rates by 82% (p<0.001) and delayed the time to first relapse; an estimated 85.7% of patients treated with Gilenya were relapse-free at 24 months, versus 38.8% of patients treated with interferon beta-1a (p<0.001)
  • Significantly reduced the number of new or newly enlarged T2 lesions up to 24 months by 53% (p<0.001). Also, it significantly reduced the average number of gadolinium enhancing T1 (Gd+) lesions per scan at 24 months by 66.0% (p<0.001). The number and volume of lesions are associated with increased relapse rates and disability progression
  • In additional analyses, significantly reduced the annualized rate of brain volume loss (brain shrinkage) by 40%

The safety profile of Gilenya in this study was overall consistent with that seen in previous clinical trials in adults[3].

”PARADIGMS exemplifies Novartis’ commitment to reimagining care for young patients with neurological conditions,” said Danny Bar-Zohar, Global Head, Neuroscience Development for Novartis. ”It is pioneering in every sense of the word, demonstrating the collaborative approach taken with all stakeholders and disciplines to bring the understanding of the unique attributes of pediatric MS to the next level. Our priority now is to continue discussions with worldwide health authorities to bring Gilenya to young patients in need, as soon as possible.”

Gilenya is a well-established treatment for MS in the adult population, having been used to treat more than 255,000 patients in both clinical trials and the post-marketing setting, with approximately 566,000 years of patient experience[4].

About the Phase III PARADIGMS study

The Phase III PARADIGMS study (NCT01892722) is a flexible duration (up to two years), double-blind, randomized, multi-center study to evaluate the safety and efficacy of oral Gilenya® (fingolimod) compared to interferon beta-1a in children and adolescents with a confirmed diagnosis of multiple sclerosis (MS), followed by a five-year open label extension phase[3]. The study enrolled 215 children and adolescents with MS, 10 to less than 18 years of age with an Expanded Disability Status Scale (EDSS) score between 0 and 5.5[3]. Patients were randomized to receive once-daily oral Gilenya (0.5 mg or 0.25 mg, dependent on patients’ body weight) or intramuscular interferon beta-1a once weekly[3].

The primary endpoint of the study was the frequency of relapses in patients treated up to 24 months (annualized relapse rate)[3]. Secondary endpoints include the number of new or newly enlarged T2 lesions, gadolinium-enhancing T1 lesions, safety and the pharmacokinetic properties of Gilenya, all measured throughout the treatment period[3].

The Phase III PARADIGMS study was conducted in 80 centers in 25 countries, and was designed in partnership with the US Food and Drug Administration, the European Medicines Agency and the International Pediatric Multiple Sclerosis Study Group[3].

References

[1]    Waldman A et al. Pediatric multiple sclerosis. Neurology. 2016; 87(9): S74-S81.

[2]    MS Society. Children and MS. https://www.mssociety.org.uk/what-is-ms/types-of-ms/ms-in-children#MS%20and%20school (link is external). Accessed September 2018.

[3]    Chitnis T et al. Trial of Fingolimod versus Interferon Beta-1a in Pediatric Multiple Sclerosis. NEJM 2018; 379(11): 1017-1027.

[4]    Novartis data on file.

[5]    PubMed Heath. Multiple Sclerosis (MS). http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001747/ (link is external). Accessed September 2018.

[6]    MS Society. Types of MS. https://www.mssociety.org.uk/what-is-ms/types-of-ms (link is external). Accessed September 2018.

[7]    Multiple sclerosis International Federation. Atlas of MS 2013. https://www.msif.org/wp-content/uploads/2014/09/Atlas-of-MS.pdf (link is external). Accessed September 2018.

[8]    Patel Y et al. Pediatric multiple sclerosis. Ann Indian Acad Neurol. 2009; 12(4): 238-245.

[9]    Gilenya US Prescribing Information. https://www.pharma.us.novartis.com/sites/www.pharma.us.novartis.com/files/gilenya.pdf (link is external). Accessed September 2018.

[10]  Brinkmann V et al. FTY720 (fingolimod) in Multiple Sclerosis: therapeutic effects in the immune and the central nervous system. Br J Pharmacol. 2009; 158(5): 1173-1182.

[11]  De Stefano N et al. Effect of fingolimod on diffuse brain tissue damage in relapsing-remitting multiple sclerosis patients. Mult Scler Relat Disord. 2016; 7: 98-101.

[12]  Warrender-Sparkes M et al. The effect of oral immunomodulatory therapy on treatment uptake and persistence in multiple sclerosis. Mult Scler. 2016; 22(4): 520-532.

[13]  Khatri B et al. Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study. Lancet Neurol. 2011; 10(6): 520-529.

[14]  Giovannoni G et al. ”No evident disease activity”: The use of combined assessments in the management of patients with multiple sclerosis. Mult Scler. 2017. Doi 10.1177/1352458517703193.

[15]  De Stefano N et al. Effect of Fingolimod on Brain Volume Loss in Patients with Multiple Sclerosis. CNS Drugs. 2017; 31(4): 289-305.

[16]  Kappos L et al. Inclusion of brain volume loss in a revised measure of ‘no evidence of disease activity’ (NEDA-4) in relapsing-remitting multiple sclerosis. Mult Scler. 2016; 22(10): 1297-1305.

[17]  Lizac N et al. Highly active immunomodulatory therapy ameliorates accumulation of disability in moderately advanced and advanced multiple sclerosis. J Neurol Neurosurg Psychiatry. 2017; 88(3): 196-203.

[18]  Gilenya EMA Summary of Product Characteristics.  http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Product_Information/human/002202/WC500104528.pdf (link is external). Accessed September 2018.