Ustekinumab biosimilar for treating inflammatory conditions
Gastrointestinal tract
6 February 2026
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Guidance Recommendations
The Ministry of Health’s Drug Advisory Committee has recommended ustekinumab biosimilar (Steqeyma) 45 mg/0.5 mL pre-filled syringe, 90 mg/1 mL pre-filled syringe, and 130 mg/26 mL vial for listing on the MOH Standard Drug List (SDL). The decision was based on the acceptable pricing proposal from the company.
Funding status
SDL subsidy will apply from 1 April 2026 to all registered indications of ustekinumab biosimilar (Steqeyma) 45 mg/0.5 mL pre-filled syringe, 90 mg/1 mL pre-filled syringe, and 130 mg/26 mL vial in Singapore.
SDL subsidy does not apply to other brand(s), formulation(s) or strength(s) of ustekinumab
Guidance_Ustekinumab biosimilar for treating inflammatory conditions (6 February 2026)
