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U.S. FDA approves first two-drug HIV regimen
November 21, 2017 / 8:12 PM / 23 days ago

U.S. FDA approves first two-drug HIV regimen

NEW YORK, Nov 21 (Reuters) - The U.S. Food and Drug Administration on Tuesday approved the first two-drug regimen to treat HIV, the virus that causes AIDS, aimed at easing the side effects for long-term patients who are on the standard treatment involving three or more drugs.

The treatment, called Juluca, is a fixed-dose tablet that combines two previously approved drugs, dolutegravir and rilpivirine, and is available to patients who have been on a stable regimen for at least six months.

Juluca belongs to GlaxoSmithKline Plc’s majority-owned ViiV Healthcare, in which Pfizer and Shionogi also have small stakes. ViiV’s dolutegravir is part of GSK’s traditional triple-therapy used to control the AIDS virus.

The approval puts GSK ahead of rival Gilead Sciences in the race to market with two-drug combinations for HIV treatments, although uptake could be slow because rilpivirine has the downside that it must be taken with a meal at the same time every day.

The FDA has a February deadline to decide on Gilead’s competing combination.

GSK is also working on a second two-drug combination that will replace rilpivirine with a common off-patent drug called 3TC that could reach the market in the second half of 2019 if clinical trials are successful. (Reporting by Caroline Humer; Editing by Bernadette Baum)

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