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. 2019 Apr-Jun;22(2):131–136. doi: 10.4103/aian.AIAN_345_18

Table 1.

Drugs in secondary progressive multiple sclerosis

Drug Year Studies Number of patients  MS type RRR Reduction in disease progression Decrease in Gd+/new T2 lesions   Conclusion
Drugs used in RRMS
 Beta IFN[13] 2012 5 1829: IFN beta
1293: Placebo
SPMS 0.91 (0.84–0.97) 0.88 (0.80–0.97) (NS) No May be used in early SPMS
 Glatiramer acetate[14] 2010 6 1049 PMS 0.81 (0.5–1.29) −0.45 (NS) No May be used in early SPMS
Immune suppressive drugs
 Mitoxantrone[15] 2013 1 194 RRMS
SPMS
−0.85 (–1.47–−0.23) 0.23 (0.09–0.59) Yes(S) Is approved in SPMS with ongoing inflammation
 Azathioprine[16] 2007 5 698 RRMS
SPMS
−0.26 (−0.43–−0.10) 0.42 (0.07–0.64) No Limited evidence
 Cyclosporine[17] 1990 1 273: CSA
274: Placebo
PMS 0.765 0.17±0.39 (NS) No Limited evidence
 MTX[18] 2004 1 31: MTX
29: Placebo
PMS NA 11/31: MTX, 15/29: Placebo (NS) No May be used in financial constraints or those with other rheumatological disorders
 CPP[19,20] 2007 4 152 SPMS NA 1.05 (0.79–1.41) No May be used
2017 1 72: CPP
66: MPS
SPMS NA 0.61 (0.31–1.22) (NS) - -
 Linomide[21] 2000 1 715 SPMS Terminated early due to ADR No evidence
 Cladiribine[22] 2000 1 Cladiribine: 105
Placebo: 54
SPMS NA 24% versus 33% (NS) Yes(S) No clinical evidence
Monoclonal antibodies
 NTZ[23] 2018 1 439: NTZ
449: Placebo
SPMS NA 0.86 (0.66–0.13) (NS) No Limited evidence
 RTX[24] - 1 RTX: 292 Placebo: 147 PMS NA Mean change in EDSS 0.33 versus 0.45 (NS) Yes(S) Limited evidence
 Alemtuzumab[25] 2017 1 15 SPMS NA −0.5 No Limited evidence
 IVIg[26,27] 2004 1 159: IVIg
159: Placebo
SPMS 0.46 1.11 (0.80–1.53) No Limited evidence
 - 2007 1 99: SPMS
98: Placebo
SPMS 0.50 versus 0.49 (NS) 48% versus 39% (NS) - -

Gd=Gadolinium, MS=Multiple sclerosis, RRMS=Relapsing-remitting MS, SPMS=Secondary progressive MS, PMS=Progressive MS, MTX=Methotrexate, CPP=Cyclophosphamide, MPS=Methylprednisolone, S=Significant, NS=Nonsignificant, IVIg=Intravenous immune globulin, RTX=Rituximab, RRR=Relative risk reduction, IFN=Interferon, CSA=Cambridge Scientific Abstracts, ADR=Adverse drug reaction, NA=Not available, NTZ=Natalizumab, EDSS=Expanded Disability Status Scale