in the absence of a submission from the holder of the marketing authorisation:
raltegravir (Isentress®) is not recommended for use within NHSScotland.
Indication under review: in combination with other anti-retroviral medicinal products in the treatment of human immunodeficiency virus in neonates.
The holder of the marketing authorisation has not made a submission to SMC regarding this product in this setting. As a result we cannot recommend its use within NHSScotland.
From January 2020, ADTCs may make formulary decisions on paediatric licence extensions for medicines previously accepted for use (or restricted use) for the corresponding indication in adults, taking account of relevant restrictions. This approach may also be applied retrospectively to medicines accepted for use in adults but not recommended in the corresponding indication in children due to absence of submission. PASAG liaises with companies to extend any PAS to include the younger age group and confirms arrangements with Boards.
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- Medicine name:
- raltegravir (Isentress)
- SMC ID:
in combination with other anti-retroviral medicinal products in the treatment of human immunodeficiency virus in neonates.
- Pharmaceutical company
- BNF chapter
- Submission type
- Non submission
- Not recommended
- Date advice published
- 09 July 2018