Impact of Natalizumab on Ambulatory Improvement in Secondary Progressive and Disabled Relapsing-remitting Multiple Sclerosis
Overview
Affiliations
Background: There is an unmet need for disease-modifying therapies to improve ambulatory function in disabled subjects with multiple sclerosis.
Objectives: Assess the effects of natalizumab on ambulatory function in disabled subjects with relapsing-remitting multiple sclerosis (RRMS) or secondary progressive multiple sclerosis (SPMS).
Methods: We retrospectively reviewed ambulatory function as measured by timed 25-foot walk (T25FW) in clinical trial subjects with an Expanded Disability Status Scale score ≥3.5, including RRMS subjects from the phase 3 AFFIRM and SENTINEL trials, relapsing SPMS subjects from the phase 2 MS231 study, and nonrelapsing SPMS subjects from the phase 1b DELIVER study. For comparison, SPMS subjects from the intramuscular interferon beta-1a (IM IFNβ-1a) IMPACT study were also analyzed. Improvement in ambulation was measured using T25FW responder status; response was defined as faster walking times over shorter (6-9-month) or longer (24-30-month) treatment periods relative to subjects' best predose walking times.
Results: There were two to four times more T25FW responders among disabled MS subjects in the natalizumab arms than in the placebo or IM IFNβ-1a arms. Responders walked 25 feet an average of 24%-45% faster than nonresponders.
Conclusion: Natalizumab improves ambulatory function in disabled RRMS subjects and may have efficacy in disabled SPMS subjects. Confirmation of the latter finding in a prospective SPMS study is warranted.
Drug Delivery to the Brain: Recent Advances and Unmet Challenges.
Bhunia S, Kolishetti N, Vashist A, Arias A, Brooks D, Nair M Pharmaceutics. 2023; 15(12).
PMID: 38139999 PMC: 10747851. DOI: 10.3390/pharmaceutics15122658.
Pardridge W Front Drug Deliv. 2023; 3.
PMID: 37583474 PMC: 10426772. DOI: 10.3389/fddev.2023.1227816.
Protein and Gene Delivery Systems for Neurodegenerative Disorders: Where Do We Stand Today?.
Siafaka P, Okur M, Erim P, Caglar E, Ozgenc E, Gundogdu E Pharmaceutics. 2022; 14(11).
PMID: 36365243 PMC: 9698227. DOI: 10.3390/pharmaceutics14112425.
What Have Failed, Interrupted, and Withdrawn Antibody Therapies in Multiple Sclerosis Taught Us?.
Kramer J, Wiendl H Neurotherapeutics. 2022; 19(3):785-807.
PMID: 35794296 PMC: 9294122. DOI: 10.1007/s13311-022-01246-3.
Involvement of cytotoxic Eomes-expressing CD4 T cells in secondary progressive multiple sclerosis.
Raveney B, Sato W, Takewaki D, Zhang C, Kanazawa T, Lin Y Proc Natl Acad Sci U S A. 2021; 118(11).
PMID: 33836594 PMC: 7980371. DOI: 10.1073/pnas.2021818118.