Drug class
Antiviral-HIV-1 Integrase Strand Transfer Inhibitors
Antiviral HIV-1 integrase strand transfer inhibitors (INSTIs) are a key therapeutic drug class of antiretroviral agents used for the treatment and prevention of human immunodeficiency virus type 1 (HIV-1) infection. Read more about Antiviral-HIV-1 Integrase Strand Transfer Inhibitors
24 drugs in this class 7 manufacturers
Drugs in Antiviral-HIV-1 Integrase Strand Transfer Inhibitors
ISENTRESS (raltegravir potassium)
ISENTRESS (raltegravir potassium)
TIVICAY (dolutegravir sodium)
BIXLENVO (bictegravir sodium/lenacapavir sodium)
BIXLENVO-SUNLENCA (bictegravir sodium/lenacapavir sodium)
Antiviral HIV-1 integrase strand transfer inhibitors (INSTIs) are a key therapeutic drug class of antiretroviral agents used for the treatment and prevention of human immunodeficiency virus type 1 (HIV-1) infection.
These agents selectively bind to the active site of the virally encoded integrase enzyme, specifically preventing the strand transfer reaction necessary for integrating synthesized viral DNA into the host cell genome.
By halting viral replication, they lower plasma HIV-1 RNA levels and allow reconstitution of immune function.
Members of this class, such as dolutegravir, bictegravir, and cabotegravir, serve as core components in first-line combination regimens for managing HIV-1 and as agents for pre-exposure prophylaxis.
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nih.gov
Antiviral HIV-1 integrase strand transfer inhibitors (INSTIs) are a key therapeutic drug class of antiretroviral agents used for the treatment and prevention of human immunodeficiency virus type 1 (HIV-1) infection Members of this class, such as dolutegravir, bictegravir, and cabotegravir, serve as core components in first-line combination regimens for managing HIV-1 and as agents for pre-exposure prophylaxis
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hiv.gov
Antiviral HIV-1 integrase strand transfer inhibitors (INSTIs) are a key therapeutic drug class of antiretroviral agents used for the treatment and prevention of human immunodeficiency virus type 1 (HIV-1) infection Members of this class, such as dolutegravir, bictegravir, and cabotegravir, serve as core components in first-line combination regimens for managing HIV-1 and as agents for pre-exposure prophylaxis
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fda.gov
These agents selectively bind to the active site of the virally encoded integrase enzyme, specifically preventing the strand transfer reaction necessary for integrating synthesized viral DNA into the host cell genome
-
nih.gov
These agents selectively bind to the active site of the virally encoded integrase enzyme, specifically preventing the strand transfer reaction necessary for integrating synthesized viral DNA into the host cell genome
-
nih.gov
By halting viral replication, they lower plasma HIV-1 RNA levels and allow reconstitution of immune function
-
nih.gov
By halting viral replication, they lower plasma HIV-1 RNA levels and allow reconstitution of immune function Members of this class, such as dolutegravir, bictegravir, and cabotegravir, serve as core components in first-line combination regimens for managing HIV-1 and as agents for pre-exposure prophylaxis
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