| Ticker | Status | Jurisdiction | Filing Date | CP Start | CP End | CP Loss | Deadline |
|---|
| Ticker | Case Name | Status | CP Start | CP End | Deadline | Settlement Amt |
|---|
| Ticker | Name | Date | Analyst Firm | Up/Down | Target ($) | Rating Change | Rating Current |
|---|
New data from the pivotal Phase 3 POETYK PsA-1 trial demonstrated that Sotyktu improved and maintained meaningful clinical responses, inhibition of radiographic progression and patient-reported outcomes through Week 52 in adults with active psoriatic arthritis
Safety in POETYK PsA-1 through Week 52 was consistent with the known Sotyktu profile, with no new signals identified
In the Phase 2 PAISLEY-SLE and PAISLEY long-term extension studies, sustained efficacy and consistent safety were observed with up to four years of Sotyktu treatment for moderate-to-severe systemic lupus erythematosus
Bristol Myers Squibb (NYSE:BMY) today announced Week 52 data from the pivotal Phase 3 POETYK PsA-1 trial further confirming the efficacy and safety of Sotyktu (deucravacitinib) in adults with active psoriatic arthritis (PsA) who were not previously treated with a biologic disease-modifying antirheumatic drug (bDMARD). The company also announced new findings from an integrated analysis of the Phase 2 PAISLEY-SLE and PAISLEY long-term extension (LTE) studies supporting the safety and efficacy with up to four years of Sotyktu treatment for moderate-to-severe systemic lupus erythematosus (SLE).
These data will be presented as late-breaking abstracts (POETYK PsA-1 abstract #LB20 and PAISLEY abstract #LB10) at the American College of Rheumatology (ACR) Convergence in Chicago, Illinois taking place from October 24-29, 2025.
Posted In: BMY
