Table 3

Improvement from baseline scores in SPARCC (SI joints) and Berlin (spine) at weeks 48 and 96 of the RAPID-axSpA trial for all patients in the imaging set (observed data)

All CZP (dose combined)
NMean score at baseline (SD)*Mean score (SD)Mean change from baseline (SD)
SPARCC (SI joints)
Week 48
 axSpA1139.0 (13.3)2.7 (5.7)−6.3 (12.7)
 r-axSpA619.6 (14.9)2.0 (4.5)−7.6 (13.0)
 nr-axSpA528.3 (11.3)3.5 (6.9)−4.8 (12.2)
Week 96
 axSpA1259.2 (13.1)2.1 (6.2)−7.2 (12.6)
 r-axSpA779.5 (14.1)1.4 (5.6)−8.1 (12.7)
 nr-axSpA488.8 (11.4)3.2 (7.0)−5.6 (12.4)
Berlin (spine)
Week 48
 axSpA1143.8 (5.7)1.4 (2.6)−2.4 (4.4)
 r-axSpA624.6 (5.6)1.7 (3.2)−2.9 (4.0)
 nr-axSpA522.9 (5.7)1.0 (1.5)−1.9 (4.7)
Week 96
 axSpA1264.7 (6.2)1.4 (2.5)−3.3 (5.1)
 r-axSpA785.6 (6.3)1.6 (2.9)−4.0 (5.1)
 nr-axSpA483.3 (5.9)1.0 (1.7)−2.3 (5.0)
  • Patients randomised to placebo at baseline received CZP from week 16 (if escaping early), or week 24 (if completing double-blind phase) and are included in weeks 48 and 96 results.

  • *Matched baseline readings; in the week 96 reading campaign, MRIs from each previous visit were re-read.

  • axSpA, axial spondyloarthritis; CZP, certolizumab pegol; nr-axSpA, non-radiographic axial spondyloarthritis; r-axSpA, radiographic axial spondyloarthritis; SI, sacroiliac; SPARCC, Spondyloarthritis Research Consortium of Canada.