The OTEZLA® international website

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Sustained resolution of preexisting dactylitis up to 3 years1,a

aPALACE 1-3 pooled analysis. Data as observed; includes all patients who received OTEZLA 30 mg BID, regardless of whether they were initially randomized to OTEZLA 30 mg BID or placebo patients who were re-randomized to OTEZLA at week 16 or week 24.

Patients treated with OTEZLA 30 mg BID achieved significantly greater improvement vs placebo in dactylitis count (mean change of -1.8 vs -1.3, P = 0.0097) at week 241†

*Pooled patient data from PALACE 1-3; includes all randomized patients with dactylitis (baseline dactylitis count >0; n = 633). Resolution was defined as a dactylitis count of 0.

LOCF; for patients who qualified for early escape at week 16, the week 16 value was carried forward.

BID, twice daily; LOCF, last observation carried forward; PALACE, Psoriatic Arthritis Long-Term Assessment of Clinical Efficacy.


Resolution of preexisting dactylitis at months 1 and 42,a

aLAPIS-PsA study, interim analysis at 4 months. Data as observed among patients with value available at specified time point.

In a real-world clinical setting, OTEZLA led to complete resolution of dactylitis2†

*Among patients with dactylitis count >0 at baseline (n = 32/110, 29.9%).

Defined as dactylitis count = 0.

LAPIS-PsA, Study of Apremilast Use in Patients with Psoriatic Arthritic in Practice Conditions.


  1. Gladman DD, et al. Apremilast treatment and long-term (up to 156 weeks) improvements in dactylitis and enthesitis in patients with psoriatic arthritis: analysis of a large database of the phase III clinical development program. Ann Rheum Dis. 2017;76 (suppl 2): Abstract SAT0448.
  2. Wollenhaupt J, Vollmer M, Berger S, et al. Real-world insights on apremilast treatment in psoriatic arthritis patients: interim analysis of the multicenter LAPIS-PsA study. Presented at: the 45th Congress of the German Society of Rheumatology (DGRh); 6-9 September 2017; Stuttgart, Germany.
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