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U.S. FDA Approves Bristol Myers Squibb’s Sotyktu® (deucravacitinib) for the Treatment of Adults with Active Psoriatic Arthritis
Bristol-Myers Squibb Company (BMY)
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Source: Business Wire
Last bristol-myers squibb company earnings: 2/6 07:05 am
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US:NYSE Investor Relations: bms.com/investors.html
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Significantly more patients treated with once-daily, oral Sotyktu achieved an ACR20 response compared with placebo at Week 16 in the pivotal Phase 3 POETYK PsA-1 and POE
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