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EMA Product

Tybost

Product approved by European Medicines Agency (EU)

Basic Information

Tybost

Regulatory Information

EMEA/H/C/002572

Authorised

September 19, 2013

15

February 14, 2023

Company Information

Ireland

Carrigtohill County Cork T45 DP77

GILEAD SCIENCES IRELAND UC

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (HIV-1) infected adults and adolescents aged 12 years and older: - weighing at least 35 kg co?administered with atazanavir or - weighing at least 40 kg co?administered with darunavir.

Overview Summary

Tybost is a medicine for treating adults and adolescents from 12 years of age (and over a certain weight) who are infected with HIV-1, a virus that causes acquired immune deficiency syndrome (AIDS). Tybost does not treat HIV directly but is given to boost the effects of atazanavir or darunavir, which are used with other standard medicines to treat HIV-1. It contains the active substance cobicistat.

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