Proper Use of HIV “Cocktail” Drugs Cuts Transmission To Effectively Zero: Study

The findings of a new study suggests that the proper use of antiviral HIV “cocktail” drugs cuts the risk of transmission from one person to another down to virtually zero.

In a study published this month in the medical journal The Lancet, researchers from across Europe indicate that virally suppressive antiretroviral therapy (ART) drugs not only significantly reduce the viral load of HIV, but they also appeared to eliminate the transmission of the virus from one partner to another when no other protection was used.

The researchers conducted two prospective observational studies at 75 sites in 14 European Countries from September 2010 to July 31, 2017. They looked at gay and heterosexual couples, where one partner was HIV positive and who reported condomless sex and the use of suppressive HIV drugs.

HIV DRUGS LAWSUITS

Did you suffer kidney injuries or bone fractures on Truvada or other TDF-based HIV drugs?

Gilead HIV drugs Truvada, Atripla, Stribild, Viread and Complera have been linked to increased risks of kidney and bones injuries, which lawsuits allege may have been avoided if safer formulations had not been withheld by the manufacturer.

Learn More See If You Qualify For Compensation

According to the findings, the only incidents of HIV transmission occurred when the non-infected partner had sex with an infected person outside of their relationship. In no cases did the infected partner taking antiretroviral drugs like Truvada, Atripla, Complera and Stribild, transmit the disease to their partners.

“Our results provide a similar level of evidence on viral suppression and HIV transmission risk for gay men to that previously generated for heterosexual couples and suggest that the risk of HIV transmission in gay couples through condomless sex when HIV viral load is suppressed is effectively zero,” the researchers concluded. “Our findings support the message of the U=U (undetectable equals untransmittable) campaign, and the benefits of early testing and treatment for HIV.”

HIV Drug Toxicity Concerns

The findings of this latest study come amid growing concerns that Giliead, who developed a number of HIV drugs known as tenofovir disoproxil fumarate (TDF) drugs, knew the medications were toxic and held out on less toxic alternatives until the patents on the more toxic drugs ran out, in order to increase its profits.

The widely used drugs include Truvada, Viread, Atripla and several others. Most are combinations of several drugs required to suppress the viral load in HIV and AIDs patients.

Gilead faces a growing number of HIV drug lawsuits filed nationwide by patients who say it is now pushing less toxic tenofovir alafenamide fumarate (TAF) drugs, even though it knew the drug was safer 10 years ago. The company shelved TAF in 2004 and did not begin selling TAF-designed drugs until 2015, plaintiffs argue. Patent protections for TDF drugs began expiring last year.

0 Comments

Share Your Comments

This field is hidden when viewing the form
I authorize the above comments be posted on this page
Post Comment
Weekly Digest Opt-In

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Schedule Leading to First BioZorb Lawsuit Jury Trial in September 2025 Outlined By Court
Schedule Leading to First BioZorb Lawsuit Jury Trial in September 2025 Outlined By Court (Posted yesterday)

A federal judge has issued pretrial schedules for the first two BioZorb lawsuits to go before juries starting in September, calling for the parties to outline all the issues of contention, witnesses and facts to be presented during the bellwether early test cases.

Covidien Hernia Mesh Settlement Talks To Get Underway After Parties Select Mediator Next Week
Covidien Hernia Mesh Settlement Talks To Get Underway After Parties Select Mediator Next Week (Posted 3 days ago)

A federal magistrate judge has accepted new deadlines for expert discovery in Covidien hernia mesh lawsuits, which will also result in the selection of a mediator by February 24, to shepherd the parties through settlement negotiations.