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Adalimumab [Humira]
No
Yes
No
No
General information
Subsidy Information and Financing Scheme
Not Applicable
Drug Guidance for Subsidy
01/09/2020 Adalimumab for treating inflammatory conditions
The Ministry of Health’s Drug Advisory Committee has recommended:
Adalimumab biosimilar (Amgevita) 20 mg/0.4 ml prefilled syringe and 40 mg/0.8 ml prefilled autoinjector and syringe for treating the following inflammatory conditions in line with its registered indications in Singapore:
Adults with moderately to severely active rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, chronic plaque psoriasis, ulcerative colitis, Crohn’s disease or hidradenitis suppurativa;
Adults with non-infectious intermediate, posterior and panuveitis;
Children aged 2 years or older with chronic non-infectious anterior uveitis or polyarticular juvenile idiopathic arthritis;
Children aged 4 years or older with severe chronic plaque psoriasis;
Children aged 6 years or older with moderately to severely active Crohn’s disease or enthesitis-related arthritis; and
Children aged 12 years or older with moderate to severe hidradenitis suppurativa;
The removal of adalimumab reference biologic (Humira) 40 mg/0.8 ml prefilled autoinjector from the Medication Assistance Fund (MAF) for all indications; and
Not to list new formulations of Humira (20 mg/0.2 ml or 40 mg/0.4 ml prefilled syringe and pen) on SDL or MAF in view of unfavourable cost effectiveness compared with Amgevita at the price proposed by the manufacturer.
Subsidy status
[R] Adalimumab biosimilar (Amgevita) 20 mg/0.4 ml prefilled syringe and 40 mg/0.8 ml prefilled autoinjector and syringe are recommended for inclusion on the MOH Standard Drug List (SDL) for the abovementioned indications from 1 September 2020. The MAF listing of Humira will cease on 1 March 2021.
[NR] SDL subsidy does not apply to any formulations or strengths of Humira.
Legend
This section displays recommendation from the MOH Drug Advisory Committee for subsidy and appropriate use of the drug as extracted from the Agency for Care Effectiveness (ACE) Drug Guidances. As this website is updated monthly, please refer to the ACE website for the most updated information.
Legend list
Indicator | Legend |
|---|---|
R | Recommended for subsidy |
NR | Not recommended for subsidy |
Registered Product(s) Information
Clinical and product info
Clinical info | Product Info |
|---|---|
Information under the Indication, Dosage and Contraindication sections are extracted from the relevant Package Insert/Patient Information Leaflet of the product available on HSA Infosearch. For more information, please refer to the product's Package Insert/ Patient Information Leaflet available on HSA Infosearch. The information provided is for informational purposes only, and is not exhaustive. The information provided is not a substitute for professional medical advice. Please consult a qualified healthcare provider for any medical advice. | Information available here are product details as registered with the HSA. As this website is updated monthly, please refer to HSA Infosearch for the most updated product information. |
Subcutaneous
HUMIRA SOLUTION FOR INJECTION 20MG/0.2ML (PRE-FILLED SYRINGE) [SIN15718P]
HUMIRA SOLUTION FOR INJECTION 40MG/0.4ML (PRE-FILLED PEN) [SIN15248P]
HUMIRA SOLUTION FOR INJECTION 80MG/0.8ML (PREFILLED PEN) [SIN15914P]
HUMIRA SOLUTION FOR INJECTION 80MG/0.8ML (PREFILLED SYRINGE) [SIN15915P]
HUMIRA SOLUTION FOR INJECTION 40MG/0.4ML (PRE-FILLED SYRINGE) [SIN15786P]
