Table 1.
Clinical trial | Drug | Patient population | NEDA-3 as endpoint | NEDA-4 as endpoint |
---|---|---|---|---|
CLARITY [15] | Cladribine | RRMS | Post hoc | – |
OPERA I/II [16] | Ocrelizumab | RMS | Secondary | – |
CASTING [17] | Ocrelizumab | RRMS | Primary | – |
CHORDS [18] | Ocrelizumab | RRMS | Primary | – |
ASCLEPIOS I/II [19, 20] | Ofatumumab | RMS | Exploratory | Secondary |
OPTIMUM [21] | Ponesimod | RMS | Exploratory | Exploratory |
ULTIMATE I/II [7] | Ublituximab | RMS | Secondary | – |
DEFINE/CONFIRM [22] | Dimethyl fumarate | RRMS | Post hoc | – |
AFFIRM [14] | Natalizumab | RRMS | Post hoc | – |
STRIVE [23] | Natalizumab | RRMS | Primary | – |
FREEDOMS [24] | Fingolimod | RRMS | Exploratory | Post hoc |
PANGAEA 2.0 [25] | Fingolimod | RRMS | – | |
ADVANCE/ATTAIN [26, 27] | Peginterferon-β1a | RRMS | Post hoc | – |
PRISMS [28] | Interferon-β1a | RRMS | Exploratory | – |
EVIDENCE [29] | Interferon-β1a | RRMS | Post hoc | – |
NEDA no evidence of disease activity, NEDA-3 3-parameter no evidence of disease activity, NEDA-4 4-parameter no evidence of disease activity, RMS relapsing multiple sclerosis, RRMS relapsing–remitting multiple sclerosis