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EMA Product

Dovato

Product approved by European Medicines Agency (EU)

Basic Information

Dovato

Regulatory Information

EMEA/H/C/004909

Authorised

June 10, 2022

April 26, 2019

17

December 10, 2024

Company Information

the netherlands

Van Asch van Wijckstraat 55 H 3811 LP Amersfoort

ViiV Healthcare BV

Active Substances Detail

dolutegravir sodiumlamivudine

Detailed Information

Therapeutic Indication

### Therapeutic indication Dovato is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in adults and adolescents above 12 years of age weighing at least 40 kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine.

Overview Summary

Dovato is a medicine for treating infection with human immunodeficiency virus type 1 (HIV-1), a virus that causes acquired immune deficiency syndrome (AIDS). It is used to treat adults and adolescents over 12 years old who weigh at least 40 kg. This medicine contains the active substances dolutegravir and lamivudine and is used to treat infections that are not resistant to medicines of the same class as dolutegravir or to lamivudine.

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