FDA Approves SOTYKTU — E.R. Squibb & Sons, L.L.C.
The FDA has granted approval to Squibb’s oral drug SOTYKTU (deucravacitinib) for the treatment of moderate-to-severe plaque psoriasis, a development that may allow the pharmaceutical giant to accelerate its entry into the highly competitive biologic segment while diversifying its revenue streams beyond the oncology niche.
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.
Get real-time financial news in your trading bot or app
GET FREE KEY — 10,000 calls/day