- Takeda disclosed new Phase 3 data for investigational oral TYK2 inhibitor zasocitinib (TAK-279) in moderate-to-severe plaque psoriasis, already presented March 28 at 2026 American Academy of Dermatology Annual Meeting.
- Latitude PsO 3001 and 3002 showed about 70% of patients achieved sPGA 0/1 at week 16, versus about 11%–13% on placebo.
- Week 16 PASI 90 reached 61.3% in one study, 51.9% in other study, versus 5% or less on placebo.
- Latitude PsO 3002 showed PASI 75 at week 4 of 16.8%, versus 4.3% on placebo.
- Takeda targets New Drug Application submissions starting in fiscal 2026, with expected psoriasis launch timing shown as 2027 H1 pending regulatory review.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Takeda Pharmaceutical Co. Ltd. published the original content used to generate this news brief via Singapore Exchange Limited (SGX) (Ref. ID: FUO8M3WJPA1OR96Z) on March 30, 2026, and is solely responsible for the information contained therein.
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