Highlights
- •The phase 4 Evaluate Patient OutComes study was conducted in North America.
- •Patients switched directly from an injectable DMT to fingolimod without a washout.
- •Most self-reported outcomes significantly improved 6 months after the switch.
- •The EPOC study broadens knowledge of fingolimod use in a real-world scenario.
Abstract
Background
Methods
Results
Conclusion
Keywords
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Multiple Sclerosis and Related DisordersReferences
- Cost-effectiveness of early initiation of fingolimod versus delayed initiation after 1 year of intramuscular interferon beta-1a in patients with multiple sclerosis.Clin Ther. 2012; 34: 1583-1590
- Psychometric evaluation of the Beck Depression Inventory-II with primary care medical patients.Health Psychol. 2001; 20: 112-119
- Validation of a general measure of treatment satisfaction, the Treatment Satisfaction Questionnaire for Medication (TSQM), using a national panel study of chronic disease.Health Qual Life Outcomes. 2004; 2: 12
- Improving adherence to injectable disease-modifying drugs in multiple sclerosis.Expert Opin Drug Deliv. 2013; 10: 285-287
- The validity of the CGI severity and improvement scales as measures of clinical effectiveness suitable for routine clinical use.J Eval Clin Pract. 2008; 14: 979-983
- A review of disease-modifying therapies for MS: maximizing adherence and minimizing adverse events.Curr Med Res Opin. 2009; 25: 77-92
- Fingolimod (FTY720): discovery and development of an oral drug to treat multiple sclerosis.Nat Rev Drug Discov. 2010; 9: 883-897
- What do effective treatments for multiple sclerosis tell us about the molecular mechanisms involved in pathogenesis?.Int J Mol Sci. 2012; 13: 12665-12709
- Safety and efficacy of fingolimod in patients with relapsing-remitting multiple sclerosis (FREEDOMS II): a double-blind, randomised, placebo-controlled, phase 3 trial.Lancet Neurol. 2014; 13: 545-556
- Randomized, open-label study to evaluate patient-reported outcomes with fingolimod after changing from prior disease-modifying therapy for relapsing multiple sclerosis: EPOC study rationale and design.J Med Econ. 2013; 16: 859-865
- Oral fingolimod (FTY720) treatment improves the performance of daily activities compared with intramuscular interferon α-1a: patient-reported indices for multiple sclerosis (PRIMUS)-activities results from a phase III study (TRANSFORMS).Neurology. 2010; 74: A543
- Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis.N Engl J Med. 2010; 362: 402-415
- The development of patient-reported outcome indices for multiple sclerosis (PRIMUS).Mult Scler. 2009; 15: 1092-1102
Francis G., Kappos L., O’Connor P., Collins W., Zhang-Auberson L., de Vera A., et al. Lymphocytes and fingolimod - temporal pattern and relationship with infections. 2010; P442: Poster presented at the 26th Congress of the European Committee for Treatment and Research in Multiple Sclerosis, 13–16 October 2010, Gothenburg, Sweden
- FTY720 preferentially depletes naive T cells from peripheral and lymphoid organs.Int Immunopharmacol. 2006; 6: 1902-1910
ICH. ICH harmonised tripartite guidelines for good clinical practice E6(R1). In: Proceedings of the International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use, Geneva 〈http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E6_R1/Step4/E6_R1__Guideline.pdf〉 [accessed 27.02.14] 1996.
ICH. In: Proceedings of the international conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (ICH) 〈http://www.ich.org/products/guidelines.html〉 [27.02.14] 2013.
- Quality of life in patients with multiple sclerosis: the impact of fatigue and depression.J Neurol Sci. 2002; 205: 51-58
- Assessment of the SF-36 version 2 in the United Kingdom.J Epidemiol Community Health. 1999; 53: 46-50
- Randomized cross-over study of patient preference for oral or intravenous vinorelbine in combination with carboplatin in the treatment of advanced NSCLC.Lung Cancer. 2008; 62: 85-91
- A placebo-controlled trial of oral fingolimod in relapsing multiple sclerosis.N Engl J Med. 2010; 362: 387-401
- Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS).Neurology. 1983; 33: 1444-1452
- Glatiramer acetate for multiple sclerosis.Cochrane Database Syst Rev. 2010; : CD004678
- Randomized crossover trial of intravenous 5-FU versus oral UFT both modulated by leucovorin: a one-centre experience.Eur J Cancer Care. 2005; 14: 151-154
- A meta-analysis of the efficacy and tolerability of interferon-beta in multiple sclerosis, overall and by drug and disease type.Clin Ther. 2010; 32: 1871-1888
- Interferon therapy in relapsing-remitting multiple sclerosis: a systematic review and meta-analysis of the comparative trials.J Neurol Sci. 2011; 302: 96-105
- Quality of life related to oral versus subcutaneous iron chelation: a time trade-off study.Value Health J Int Soc Pharmacoecon Outcomes Res. 2007; 10: 451-456
- [Adherence to and satisfaction with oral outpatient thromboembolism prophylaxis compared to parenteral: SALTO study].Rev Esp Cir Ortop Traumatol. 2013; 57: 53-60
- Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria".Ann Neurol. 2005; 58: 840-846
- Benefit-risk analysis of glatiramer acetate for relapsing-remitting and clinically isolated syndrome multiple sclerosis.Clin Ther. 2012; 34 (, e5): 159-176
- Interferon in relapsing-remitting multiple sclerosis.Cochrane Database Syst Rev. 2001; : CD002002
- Immunology of multiple sclerosis.Annu Rev Immunol. 2005; 23: 683-747
- Impact of adherence to disease-modifying therapies on clinical and economic outcomes among patients with multiple sclerosis.Adv Ther. 2011; 28: 51-61
- Factors that influence adherence with disease-modifying therapy in MS.J Neurol. 2009; 256: 568-576
- Factors that influence adherence with disease-modifying therapy in MS.J Neurol. 2009; 256: 568-576
- A randomised cross-over trial comparing patient preference for oral capecitabine and 5-fluorouracil/leucovorin regimens in patients with advanced colorectal cancer.Ann Oncol Off J Eur Soc Med Oncol / ESMO. 2006; 17: 239-245
US prescribing information. Gilenya prescribing information. 〈https://www.pharma.us.novartis.com/product/pi/pdf/gilenya.pdff〉 [accessed 03.14]2014.
- Validation of the fatigue severity scale in a Swiss cohort.Sleep. 2008; 31: 1601-1607
- The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course.Brain. 1989; 112: 1419-1428
World Medical Association. Declaration of Helsinki: Ethical principles for medical research involving human subjects. www.wma.net/en/30publications/10policies/b3/index.html [27.02.14] 2014
- Interim results of the PANGAEA and PEARL studies, comparing treatment satisfaction and pharmaco-economic data of fingolimod (Gilenya®) and first-line therapies in multiple sclerosis patients in Germany.Neurology. 2013; 80 P03: 220
Article info
Publication history
Identification
Copyright
ScienceDirect
Access this article on ScienceDirectLinked Article
- First-dose effects of fingolimod after switching from injectable therapies in the randomized, open-label, multicenter, Evaluate Patient OutComes (EPOC) study in relapsing multiple sclerosisMultiple Sclerosis and Related DisordersVol. 3Issue 5