Dolutegravir: A New Integrase Strand Transfer Inhibitor for the Treatment of HIV
The first two integrase strand transfer inhibitors (INSTIs) approved for treatment of patients infected with human immunodeficiency virus (HIV) were raltegravir and elvitegravir. Both raltegravir and elvitegravir are now guideline‐preferred agents as part of an antiretroviral regimen for treatment‐n...
Saved in:
Published in: | Pharmacotherapy Vol. 34; no. 5; pp. 506 - 520 |
---|---|
Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Boston, MA
Blackwell Publishing Ltd
01-05-2014
Pharmacotherapy Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The first two integrase strand transfer inhibitors (INSTIs) approved for treatment of patients infected with human immunodeficiency virus (HIV) were raltegravir and elvitegravir. Both raltegravir and elvitegravir are now guideline‐preferred agents as part of an antiretroviral regimen for treatment‐naive patients. However, raltegravir is dosed twice/day. Elvitegravir is available in a single‐tablet regimen and dosed once/day because it is administered with the pharmacokinetic booster cobicistat, a potent CYP3A4 inhibitor that can lead to clinically significant drug–drug interactions. In addition, raltegravir and elvitegravir have a low genetic barrier to resistance and are associated with cross‐resistance. Dolutegravir is a new‐generation INSTI administered once/day without a pharmacokinetic booster and can be coformulated in a single‐tablet regimen. Phase III studies have demonstrated the efficacy and safety of dolutegravir for treatment‐naive and treatment‐experienced patients. Compared with other INSTIs, dolutegravir has a higher genetic barrier to resistance. Dolutegravir was approved by the U.S. Food and Drug Administration in August 2013 and joins raltegravir and elvitegravir as guideline‐preferred agents for the management for HIV‐infected treatment‐naive patients. |
---|---|
Bibliography: | ArticleID:PHAR1386 ark:/67375/WNG-BJVZ65S3-J istex:03EEC2D3636B445ED202B1508E4A3CAC16C3FF21 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0277-0008 1875-9114 |
DOI: | 10.1002/phar.1386 |