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Significant itch improvement

PRIME 18+ YEARS

Proportion of patients with ≥4-point
improvement in WI-NRS AT WEEK 24

(primary endpoint)1-3,a
  • A nominal difference was observed at Week 4 (19% with DUPIXENT vs 4% with placebo)3

PRIME2 18+ YEARS

  • A nominal difference was observed at Week 11 (33% with DUPIXENT vs 17% with placebo), with a significantly greater proportion of DUPIXENT patients achieving a meaningful response at Week 12 (37% with DUPIXENT vs 22% with placebo; P=0.022, primary endpoint). At Week 24, 58% of DUPIXENT patients achieved significant itch relief vs 20% with placebo (P <0.001, secondary endpoint)1-3
PRIME and PRIME2
Pooled analysis
Itch improvement observed after first dose (as measured at Week 2)4
  • 7.8% of DUPIXENT patients had ≥4-point improvement in WI-NRS at Week 2 vs 1.9% with placebo3,4
  • 59% of DUPIXENT patients had ≥4-point improvement in WI-NRS at Week 24 vs 19% with placebo3,4

Definitive conclusions cannot be made for these results as the data were not multiplicity controlled and P values were nominal.

DUPIXENT showed consistent efficacy regardless of patients’ atopic background1,5

PRIME and PRIME2
Pooled analysis

Itch improvement regardless of patients’ history of atopy

Proportion of patients with ≥4-point improvement in WI-NRS at Week 241,5

Definitive conclusions cannot be made for these results as the data were not
multiplicity controlled and P values were nominal.

In the PRIME trials, patients were stratified by their history of atopy.

PN is a chronic and distinct dermatologic disease
57 percent
of patients across PRIME and PRIME2 did not have a history of atopy (defined as having a medical history of atopic dermatitis, allergic rhinitis/rhinoconjunctivitis, asthma, or food allergy)1

IGA PN-S, Investigator’s Global Assessment PN-Stage; PN, prurigo nodularis; Q2W, once every 2 weeks; SD, standard deviation; WI-NRS, Worst Itch numerical rating scale.