US FDA approves ViiV's Triumeq PD for children

31 March 2022

Specialist HIV company ViiV Healthcare, which is majority-owned by GlaxoSmithKline (LSE: GSK), says that the US Food and Drug Administration has approved a new drug application (NDA) for a dispersible tablet formulation of the fixed dose combination of abacavir, dolutegravir and lamivudine for the treatment of pediatric patients weighing 10kgs to <25 kgs with human immunodeficiency virus type 1 (HIV-1).

In addition, a supplemental new drug application (sNDA) has been approved for Triumeq, tablet, lowering the minimum weight that a child with human immunodeficiency virus type 1 (HIV-1) can be prescribed this medicine to 25kgs from 40kgs.

The news comes just a day after the FDA cleared ViiV’s Cabenuva (cabotegravir/rilpivirine) for a new indication.

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