Ilumya / Ilumetri phase 3 for psoriatic arthritis

[Fred]

Sun Pharma today announced top-line results from two Phase 3 clinical studies evaluating the efficacy and safety of Ilumya / Ilumetri (tildrakizumab) 100 mg administered over 24 weeks for treatment of active psoriatic arthritis.

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Treatment with tildrakizumab 100 mg resulted in greater improvements in PsA signs and symptoms at week 24 compared to treatment with placebo.

Both the INSPIRE-1 and INSPIRE-2 studies achieved the primary endpoint, with a higher proportion of patients in the INSPIRE-1 and INSPIRE-2 studies treated with tildrakizumab achieving ACR20 responses at week 24, compared to those receiving placebo (p < 0.05).

"We are excited to share that both the INSPIRE-1 and INSPIRE-2 clinical trials have successfully met their primary endpoints. These top-line results reinforce the therapeutic potential of tildrakizumab as a treatment option for patients with active psoriatic arthritis. We extend our sincere gratitude to the patients, healthcare professionals and administrators whose contributions made the studies possible. We look forward to sharing the complete clinical data in the near future"

Safety data in the studies was consistent with the well-documented safety profile of tildrakizumab, which is approved for the treatment of adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or
phototherapy.

No new safety signals were identified in the INSPIRE-1 and INSPIRE-2 studies. Findings from the INSPIRE studies will be presented at upcoming medical conferences and published in a peer-reviewed medical journal. Use of tildrakizumab 100 mg in psoriatic arthritis is not approved, and its safety and efficacy have not been evaluated by regulatory authority

Source: sunpharma.com

Ilumetri / Ilumya (tildrakizumab)