Abstract:
Objective. To assess non-inferiority of s.c. to i.v. CT-P13 in RA.
Methods. Patients with active RA and inadequate response to MTX participated in this phase I/III double-blind study at
76 sites. Patients received CT-P13 i.v. 3 mg/kg [week (W) 0 and W2] before randomization (1:1) at W6 to CT-P13 s.c. via
pre-filled syringe (PFS) 120mg biweekly until W28, or CT-P13 i.v. 3 mg/kg every 8 weeks until W22. Randomization was
stratified by country, W2 serum CRP and W6 body weight. From W30, all patients received CT-P13 s.c. In a usability substudy,
patients received CT-P13 s.c. via auto-injector (W46–54) then PFS (W56–64). The primary endpoint was change
(decrease) from baseline in disease activity score in 28 joints (DAS28)-CRP at W22 (non-inferiority margin: 0.6).
Results. Of 357 patients enrolled, 343 were randomized to CT-P13 s.c. (n¼167) or CT-P13 i.v. (n¼176) at W6. The
least-squares mean change (decrease) from baseline (standard error) in DAS28-CRP at W22 was 2.21 (0.22) for CT-P13
s.c. (n¼162) and 1.94 (0.21) for CT-P13 i.v. [n¼168; difference 0.27 (95% CI: 0.02, 0.52)], establishing non-inferiority.
Efficacy findings were similar between arms at W54. Safety was similar between arms throughout: 92 (54.8%; CT-P13
s.c.) and 117 (66.9%; CT-P13 i.v.) patients experienced treatment-emergent adverse events (from W6). There were no
treatment-related deaths or new safety findings. Usability was similar for CT-P13 s.c. via auto-injector or PFS.
Conclusion. CT-P13 s.c. was non-inferior to CT-P13 i.v. in active RA. The convenience of s.c. administration
could benefit patients.
Trial registration. ClinicalTrials.gov, https://clinicaltrials.gov/ct2/show/NCT03147248.
