Table 3.
Author (Year) | Design | Biosimilar Product | Indication | Switched Population | Baseline ADA n/N (%) | Follow-up (Weeks) |
---|---|---|---|---|---|---|
Double-blinded studies | ||||||
Griffiths et al. (2017)48 | MC PRO RCT | Erelzi | PsO | 100a 96b |
- | 40 |
Gerdes et al. (2017)49 | MC PRO RCT | Erelzi | PsO | 196c | - | 18 |
Open-label studies | ||||||
Emery et al. (2017)50 | MC PRO OBS | Brenzys | RA | 119 | 48 |
aPatients receiving GP2015 for period 1 then switched to etanercept→GP2015→etanercept, which continued into extension.
bPatients receiving etanercept for period 1 then switched to GP2015→etanercept→GP2015, which continued into extension.
cIncludes patients from Griffiths et al. (2017)48 who were either switched from a reference to biosimilar or biosimilar to reference product.
ADA = antidrug antibody; MC = multicenter; OBS = observational; PRO = prospective; PsO = psoriasis; RA = rheumatoid arthritis; RCT = randomized controlled trial.