U.S approves first injectable PrEP medication to lower HIV risk

The
US Food and Drug Administration has approved the first injectable medication
for pre-exposure prophylaxis (PrEP) to lower the risk of getting HIV through
sex, it announced Monday.
Apretude
is approved for adults and teens who are at risk of getting HIV through sex and
who weigh at least 77 pounds. It's given first as two shots a month apart, and
every two months afterward.
PrEP
was previously available only in the form of pills, Truvada and Descovy.
"Today's
approval adds an important tool in the effort to end the HIV epidemic by
providing the first option to prevent HIV that does not involve taking a daily
pill," said Dr. Debra Birnkrant, director of the Division of Antivirals in
the FDA's Center for Drug Evaluation and Research.
Approval
of the new drug "will be critical to addressing the HIV epidemic in the
U.S., including helping high-risk individuals and certain groups where
adherence to daily medication has been a major challenge or not a realistic
option," Birnkrant added.
An
estimated 34,800 new cases of HIV were diagnosed in 2019, the latest year for
which federal statistics are available. That's down from 37,800 in 2015. Data
from the Centers for Disease Control and Prevention show that in 2020, PrEP was
recommended for about 1.2 million people, but only a quarter got a prescription
for it.
Two
double-blind clinical trials comparing Apretude with Truvada found
significantly lower HIV risk in people getting the injection, the FDA noted.
The risk was 69% lower in the first trial, of HIV-negative cisgender men and
transgender women who have sex with men, and 90% lower in the second trial,
which involved cisgender women.
Research
also found that Apretude was more likely than Truvada to cause side effects
such as injection site reactions, headache, fatigue, back pain, myalgia and
rash.
Because
of a risk of drug-resistant HIV variants, Apretude is only for people who test
negative for HIV immediately before starting the drug and before each
injection. The label also includes warnings about hypersensitivity reactions,
liver damage and depressive disorders.
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