- Primary Endpoint: The study met its primary endpoint, with 48.5% of patients achieving a scalp-specific Physician’s Global Assessment response of zero or one (clear/almost clear) at week 16, compared to 13.7% on placebo.
- Key Secondary Endpoints: At week 16, a significantly higher percentage of patients achieved at least a 90% improvement in Psoriasis Scalp Severity Index response and a notable change from baseline in scalp-specific itch with Sotyktu treatment compared to placebo.
Bristol Myers Squibb Announces Positive Data for Sotyktu in Moderate to Severe Psoriasis
Bristol Myers Squibb has revealed encouraging results from a phase 3b/4 study of Sotyktu, an oral TYK2 inhibitor, for treating moderate-to-severe scalp psoriasis. The study showed significant improvements in scalp-specific Physician’s Global Assessment response and Psoriasis Scalp Severity Index, with Sotyktu outperforming placebo. The findings were presented at the European Academy of Dermatology and Venereology Congress, highlighting Sotyktu's potential as a systemic therapy for psoriasis, particularly in cases involving the scalp.

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Bristol Myers Squibb's Sotyktu showed positive results in treating moderate-to-severe scalp psoriasis in the PSORIATYK S...