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US approves Gilead’s twice-yearly injection to prevent HIV

Gilead's twice-yearly injection to prevent HIV has received approval from the US Food and Drug Administration
Gilead's twice-yearly injection to prevent HIV has received approval from the US Food and Drug Administration - Copyright GETTY IMAGES NORTH AMERICA/AFP/File JUSTIN SULLIVAN
Gilead's twice-yearly injection to prevent HIV has received approval from the US Food and Drug Administration - Copyright GETTY IMAGES NORTH AMERICA/AFP/File JUSTIN SULLIVAN
Issam AHMED

The US Food and Drug Administration on Wednesday approved Gilead Sciences’ twice-yearly injection to prevent HIV — a move the company hailed as a major breakthrough in the fight against the sexually transmitted virus.

Drugs to prevent HIV transmission, known as pre-exposure prophylaxis or PrEP, have existed for more than a decade. But because they typically require taking a daily pill, they have yet to make a significant dent in global infections.

“This is a historic day in the decades-long fight against HIV,” Gilead chairman and chief executive Daniel O’Day said in a statement.

Lenacapavir, marketed under the brand name Yeztugo, has been shown to reduce the risk of HIV transmission by more than 99.9 percent in adults and adolescents — making it functionally akin to a powerful vaccine.

The company conducted two large clinical trials. The first, involving more than 2,000 women in sub-Saharan Africa, resulted in a 100 percent reduction in infections and demonstrated superiority over the daily oral pill Truvada.

In the second trial, involving over 2,000 men and gender-diverse individuals, only two infections were recorded — a 99.9 percent prevention rate, again surpassing Truvada.

Reported side effects included injection site reactions, headache, and nausea.

Results from both trials were published in The New England Journal of Medicine, and the journal Science named lenacapavir its 2024 “Breakthrough of the Year.”

– Price concerns dampen hope –

Despite the impressive results, optimism may be tempered by the drug’s expected high cost.

An earlier long-acting HIV prevention shot — cabotegravir, which is injected every two months and was approved by the FDA in 2021 — costs tens of thousands of dollars per year and has yet to make a major global impact.

While Gilead hasn’t disclosed a price for Yeztugo, analysts estimate the US launch cost could reach $25,000 per year. Lenacapavir’s current list price for its previously approved use as a treatment for HIV is $39,000 annually, though that is expected to drop when used as a preventive.

Activists are urging Gilead to drastically cut the price to help end the HIV pandemic.

“Even high-income countries will not be able to afford widescale use of lenacapavir at prices above US $20,000 per year,” said Andrew Hill of Liverpool University, who led a team of chemists and scientists that found it could be mass-produced and sold for as little as $25 per person per year.

“To charge one thousand times more for a medicine with pandemic-ending potential would be abhorrent,” added Winnie Byanyima, under-secretary-general of the United Nations. “We cannot end AIDS with medicines that are so costly.”

The approval also comes as President Donald Trump’s administration has slashed funding for HIV treatment and prevention programs both abroad and within the United States.

AFP
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With 2,400 staff representing 100 different nationalities, AFP covers the world as a leading global news agency. AFP provides fast, comprehensive and verified coverage of the issues affecting our daily lives.

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