Etravirine indications and usage: Difference between revisions

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==Indications and Usage==


INTELENCE®1, in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral treatment-experienced patients ages 6 years and older, who have evidence of viral replication and [[HIV-1]] strains resistant to a non-nucleoside reverse transcriptase inhibitor ([[NNRTI]]) and other antiretroviral agents.
The indication for adult use is based on Week 48 analyses from 2 randomized, double-blind, placebo-controlled trials of INTELENCE®. Both studies were conducted in clinically advanced, 3-class antiretroviral (NNRTI, N[t]RTI, PI) treatment-experienced adults. The indication for pediatric use is based on 24-week analyses of a single-arm, Phase 2 trial in antiretroviral treatment-experienced pediatric subjects 6 years to less than 18 years of age [seeUse in Specific Populations (8.4)].
In treatment-experienced adult and pediatric patients, the following points should be considered when initiating therapy with INTELENCE®:
Treatment history and resistance testing should guide the use of INTELENCE® due to concerns for potential cross-resistance.
In patients who have experienced virologic failure on an NNRTI-containing regimen, do not use INTELENCE® in combination with only N[t]RTIs [seeClinical Studies (14)].
The use of other active antiretroviral agents with INTELENCE® is associated with an increased likelihood of treatment response.
The safety and efficacy of INTELENCE® have not been established in pediatric patients less than 6 years of age or in treatment-naïve adult or pediatric patients.<ref name="dailymed.nlm.nih.gov">{{Cite web  | last =  | first =  | title = INTELENCE (ETRAVIRINE) TABLET [JANSSEN PRODUCTS LP] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a9cbc29-9f15-4b24-8d86-206b82887f3d | publisher =  | date =  | accessdate =  }}</ref>


==References==
==References==

Latest revision as of 17:01, 5 January 2014

Etravirine
INTELENCE® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2]

Indications and Usage

INTELENCE®1, in combination with other antiretroviral agents, is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral treatment-experienced patients ages 6 years and older, who have evidence of viral replication and HIV-1 strains resistant to a non-nucleoside reverse transcriptase inhibitor (NNRTI) and other antiretroviral agents.

The indication for adult use is based on Week 48 analyses from 2 randomized, double-blind, placebo-controlled trials of INTELENCE®. Both studies were conducted in clinically advanced, 3-class antiretroviral (NNRTI, N[t]RTI, PI) treatment-experienced adults. The indication for pediatric use is based on 24-week analyses of a single-arm, Phase 2 trial in antiretroviral treatment-experienced pediatric subjects 6 years to less than 18 years of age [seeUse in Specific Populations (8.4)].

In treatment-experienced adult and pediatric patients, the following points should be considered when initiating therapy with INTELENCE®:

Treatment history and resistance testing should guide the use of INTELENCE® due to concerns for potential cross-resistance.

In patients who have experienced virologic failure on an NNRTI-containing regimen, do not use INTELENCE® in combination with only N[t]RTIs [seeClinical Studies (14)]. The use of other active antiretroviral agents with INTELENCE® is associated with an increased likelihood of treatment response. The safety and efficacy of INTELENCE® have not been established in pediatric patients less than 6 years of age or in treatment-naïve adult or pediatric patients.[1]

References

  1. "INTELENCE (ETRAVIRINE) TABLET [JANSSEN PRODUCTS LP]".

Adapted from the FDA Package Insert.