Global specialist HIV company ViiV Healthcare, which is majority owned by GSK (LSE: GSK) , has been granted marketing authorization by the European Medicines Agency (EMA) for Triumeq PD; a dispersible tablet of the fixed dose combination of abacavir, dolutegravir and lamivudine for children living with HIV-1 weighing 14kg to <25kg.
The authorization also includes the label extension of Triumeq tablet, lowering the minimum weight that a child with HIV-1 can be prescribed this medicine from 40kg to 25kg.
The EU approval comes nearly a year after the US Food and Drug Administration (FDA) approved the pediatric version of Triumeq in March 2022.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze