Oral ponesimod in patients with chronic plaque psoriasis: a randomised, double-blind, placebo-controlled phase 2 trial
Abstrakt
Background We assessed the efficacy, safety, and tolerability of ponesimod, an oral, selective, reversible modulator of sphingosine 1-phosphate receptor 1, in patients with moderate to severe chronic plaque psoriasis. Methods Between Sept 22, 2010, and Oct 24, 2012, patients with psoriasis area and severity index (PASI) scores higher than 10 were enrolled into this multicentre double-blind, phase 2 study.
They received 20 mg or 40 mg ponesimod or placebo once daily for 16 weeks. Those with at least 50% reduction in PASI score at 16 weeks and who were receiving ponesimod were rerandomised to receive maintenance ponesimod therapy or placebo until week 28.
The primary endpoint was reduction in PASI score from baseline of at least 75% (PASI75) at week 16. This study is registered with ClinicalTrials.gov, number NCT01208090.
Findings Of 326 patients initially randomised (20 mg ponesimod n=126, 40 mg ponesimod n=133, and placebo n=67) PASI75 was achieved at week 16 in 58 (46.0%), 64 (48.1%), and nine (13.4%), respectively. The treatment effect was significant for the two ponesimod doses (both p < 0.0001).
Of 219 patients who entered the maintenance period, PASI75 was achieved by week 28 in 35 (71.4%) of 49 who continued on 20 mg ponesimod and 41 (77.4%) of 53 on 40 mg ponesimod, and in 19 (42.2%) of 45 who swapped from 20 mg to placebo and 19 (40.4%) of 47 from 40 mg to placebo. Ponesimod was associated with dyspnoea, raised liver enzyme concentrations, and dizziness.
Interpretation Significant clinical benefit was seen at week 16 that increased with maintenance therapy.