TY - JOUR
T1 - Repurposing Licensed Drugs with Activity Against Epstein–Barr Virus for Treatment of Multiple Sclerosis
T2 - A Systematic Approach
AU - Li, Vivien
AU - McKay, Fiona C.
AU - Tscharke, David C.
AU - Smith, Corey
AU - Khanna, Rajiv
AU - Lechner-Scott, Jeannette
AU - Rawlinson, William D.
AU - Lloyd, Andrew R.
AU - Taylor, Bruce V.
AU - Morahan, Julia M.
AU - Steinman, Lawrence
AU - Giovannoni, Gavin
AU - Bar-Or, Amit
AU - Levy, Michael
AU - Drosu, Natalia
AU - Potter, Andrew
AU - Caswell, Nigel
AU - Smith, Lynne
AU - Brady, Erin C.
AU - Frost, Bruce
AU - Hodgkinson, Suzanne
AU - Hardy, Todd A.
AU - Broadley, Simon A.
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2025.
PY - 2025
Y1 - 2025
N2 - Background: Epstein–Barr virus (EBV) is implicated as a necessary factor in the development of multiple sclerosis (MS) and may also be a driver of disease activity. Although it is not clear whether ongoing viral replication is the driver for MS pathology, MS researchers have considered the prospect of using drugs with potential efficacy against EBV in the treatment of MS. We have undertaken scientific and lived experience expert panel reviews to shortlist existing licensed therapies that could be used in later-stage clinical trials in MS. Methods: A list of therapies with anti-EBV effects was developed from existing reviews. A detailed review of pre-clinical and clinical data was undertaken to assess these candidates for potential usefulness and possible harm in MS. A ‘drug-CV’ and a plain language version focusing on tolerability aspects was created for each candidate. We used validated criteria to score each candidate with an international scientific panel and people living with MS. Results: A preliminary list of 11 drug candidates was generated. Following review by the scientific and lived experience expert panels, six yielded the same highest score. A further review by the expert panel shortlisted four drugs (famciclovir, tenofovir alafenamide, maribavir and spironolactone) deemed to have the best balance of efficacy, safety and tolerability for use in MS. Conclusions: Scientific and lived experience expert panel review of anti-EBV therapies selected four candidates with evidence for efficacy against EBV and acceptable safety and tolerability for potential use in phase III clinical trials for MS.
AB - Background: Epstein–Barr virus (EBV) is implicated as a necessary factor in the development of multiple sclerosis (MS) and may also be a driver of disease activity. Although it is not clear whether ongoing viral replication is the driver for MS pathology, MS researchers have considered the prospect of using drugs with potential efficacy against EBV in the treatment of MS. We have undertaken scientific and lived experience expert panel reviews to shortlist existing licensed therapies that could be used in later-stage clinical trials in MS. Methods: A list of therapies with anti-EBV effects was developed from existing reviews. A detailed review of pre-clinical and clinical data was undertaken to assess these candidates for potential usefulness and possible harm in MS. A ‘drug-CV’ and a plain language version focusing on tolerability aspects was created for each candidate. We used validated criteria to score each candidate with an international scientific panel and people living with MS. Results: A preliminary list of 11 drug candidates was generated. Following review by the scientific and lived experience expert panels, six yielded the same highest score. A further review by the expert panel shortlisted four drugs (famciclovir, tenofovir alafenamide, maribavir and spironolactone) deemed to have the best balance of efficacy, safety and tolerability for use in MS. Conclusions: Scientific and lived experience expert panel review of anti-EBV therapies selected four candidates with evidence for efficacy against EBV and acceptable safety and tolerability for potential use in phase III clinical trials for MS.
UR - http://www.scopus.com/inward/record.url?scp=85217547943&partnerID=8YFLogxK
U2 - 10.1007/s40263-024-01153-5
DO - 10.1007/s40263-024-01153-5
M3 - Article
C2 - 39792343
AN - SCOPUS:85217547943
SN - 1172-7047
VL - 39
SP - 305
EP - 320
JO - CNS Drugs
JF - CNS Drugs
IS - 3
M1 - e12496
ER -