Long-term follow-up of patients with relapsing multiple sclerosis from the CLARITY/CLARITY Extension cohort of CLASSIC-MS: An ambispective study

Author:

Giovannoni Gavin1,Boyko Alexey2,Correale Jorge3,Edan Gilles4,Freedman Mark S5,Montalban Xavier6,Rammohan Kottil7,Stefoski Dusan8,Yamout Bassem9,Leist Thomas10,Aydemir Aida11,Borsi Laszlo12,Verdun di Cantogno Elisabetta11

Affiliation:

1. Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK

2. Department of Neurology, Neurosurgery and Medical Genetics, Federal Center of Brain Research and Neurotechnologies, Pirogov Russian National Research Medical University, Moscow, Russia

3. Department of Neurology, FLENI Institute, Buenos Aires, Argentina

4. Department of Neurology, University Hospital of Rennes, Rennes, France

5. Department of Medicine and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada

6. Department of Neurology-Neuroimmunology, Centre d’Esclerosi Múltiple de Catalunya (Cemcat), Hospital Universitario Vall d’Hebron, Barcelona, Spain

7. MS Research Center, School of Medicine, University of Miami, Miami, FL, USA

8. Department of Neurological Sciences, Rush Medical College, Chicago, IL, USA

9. Neurology Institute, Harley Street Medical Center, Abu Dhabi, UAE/American University of Beirut Medical Center, Beirut, Lebanon

10. Division of Clinical Neuroimmunology, Comprehensive MS Center, Jefferson University, Philadelphia, PA, USA

11. EMD Serono Research & Development Institute, Inc., Billerica, MA, USA, an affiliate of Merck KGaA

12. Merck Healthcare KGaA, Darmstadt, Germany

Abstract

Background: CLASSIC-MS evaluated the long-term efficacy of cladribine tablets in patients with relapsing multiple sclerosis. Objective: Report long-term mobility and disability beyond treatment courses received in CLARITY/CLARITY Extension. Methods: This analysis represents CLASSIC-MS patients who participated in CLARITY with/without participation in CLARITY Extension, and received ⩾1 course of cladribine tablets or placebo ( N = 435). Primary objective includes evaluation of long-term mobility (no wheelchair use in the 3 months prior to first visit in CLASSIC-MS and not bedridden at any time since last parent study dose (LPSD), i.e. Expanded Disability Status Scale (EDSS) score <7). Secondary objective includes long-term disability status (no use of an ambulatory device (EDSS < 6) at any time since LPSD). Results: At CLASSIC-MS baseline, mean ± standard deviation EDSS score was 3.9 ± 2.1 and the median time since LPSD was 10.9 (range = 9.3–14.9) years. Cladribine tablets–exposed population: 90.6% ( N = 394), including 160 patients who received a cumulative dose of 3.5 mg/kg over 2 years. Patients not using a wheelchair and not bedridden: exposed, 90.0%; unexposed, 77.8%. Patients with no use of an ambulatory device: exposed, 81.2%; unexposed, 75.6%. Conclusion: With a median 10.9 years’ follow-up after CLARITY/CLARITY Extension, findings suggest the sustained long-term mobility and disability benefits of cladribine tablets.

Funder

Merck

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. Relapses and Progression of Disability in Multiple Sclerosis

2. Multiple Sclerosis: Current Knowledge and Future Outlook

3. The Multiple Sclerosis International Federation. Atlas of MS: 3rd edition, 2020, https://www.msif.org/wp-content/uploads/2020/12/Atlas-3rd-Edition-Epidemiology-report-EN-updated-30-9-20.pdf (accessed 29 April 2022).

4. Effect of relapses on development of residual deficit in multiple sclerosis

5. A Placebo-Controlled Trial of Oral Cladribine for Relapsing Multiple Sclerosis

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