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Twice-Yearly HIV prevention shot shows promise in women

NCT ID NCT06101329

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Aug 18, 2026 · Updated 2 times

Summary

This study tests a new long-acting injection called lenacapavir, given every 6 months, to prevent HIV in cisgender women in the US. About 253 women will receive either the injection or daily pills (Truvada) to compare how well the drug works in the body, its safety, and how acceptable it is. The goal is to see if a twice-yearly shot could be a convenient alternative to daily medication for HIV prevention.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
lenacapavir (injection and tablet) and emtricitabine/tenofovir disoproxil fumarate (Truvada)
What this could lead to
If successful, this could offer a convenient twice-yearly injection option for HIV prevention, reducing the need for daily pills.
What could go wrong
This is an early phase 2 study with only 253 women, so results may not apply to everyone. Side effects or low acceptability could limit its use.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

253 people

The number who actually took part.

Started

Nov 2023

Expected to finish

Jan 2028

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Key Inclusion Criteria: * Report at least 1 episode of condomless vaginal or anal sex with a cisgender man in the 12 months before enrollment. * Hepatitis B virus (HBV) surface antigen (HBsAg) negative. * Self-report one or more of the following in the past 12 months (except for incarceration, which could have occurred in the past 5 years): 1\) Noninjection recreational drug use (ecstasy, cocaine, crack cocaine, methamphetamine, ketamine, 3,4-methylenedioxy-methamphetamine, or prescription drugs apart from those prescribed by a licensed provider); 2) Alcohol dependence (defined as Cut Down, Annoyed, Guilty, and Eye Opener score of 2); binge-drinking, defined as 4 or more drinks at a time; 3) History of STIs, such as gonorrhea, chlamydia, or syphilis; 4) Exchange of sex for commodities, such as drugs, money, or shelter; 5) Incarceration (jail or prison \> 24 hours within the past 5 years); 6) Two or more sexual partners who were assigned male at birth; 7) Sexual partner assigned male at birth with history of either injection or noninjection recreational drug use, sexually transmitted infections (STIs), human immunodeficiency virus (HIV) diagnosis or unknown HIV status, additional sex partners during the course of his sexual relationship with the individual, or incarceration (jail or prison \> 24 hours within the past 5 years) * Negative local rapid HIV-1/2 antibody (Ab)/antigen (Ag) test, central HIV-1/2 Ab/Ag, and HIV-1 RNA quantitative nucleic acid amplification testing (NAAT). * Estimated glomerular filtration rate (GFR) at least 60 mL/min at screening according to the Cockcroft-Gault formula for creatinine clearance (CLcr). Key Exclusion Criteria: * Self-reported history of previous positive results on an HIV test. * One or more reactive or positive HIV test result at screening or enrollment, even if HIV infection is not confirmed. * Past or current participation in HIV vaccine or HIV broadly neutralizing antibody study unless individual provides documentation of receipt of placebo (ie, not active product). * Prior use of long-acting systemic pre-exposure prophylaxis (PrEP) (including cabotegravir (CAB) or islatravir studies). * Acute viral hepatitis A or acute or chronic hepatitis B or C infection. * Severe hepatic impairment or a history of or current clinical decompensated liver cirrhosis (eg, ascites, encephalopathy, variceal bleeding, etc). Note: Other protocol defined Inclusion/Exclusion criteria may apply.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Cornell Clinical Trials Unit, New York Presbyterian Hospital - Weill Cornell Medicine

    New York, New York, 10010, United States

  • Fenway Health

    Boston, Massachusetts, 02215, United States

  • George Washington University Medical Faculty Associates

    Washington D.C., District of Columbia, 20037, United States

  • Harlem Prevention Center CRS

    New York, New York, 10027, United States

  • ICAP at Columbia University - Bronx Prevention Center

    The Bronx, New York, 10451, United States

  • NC TraCS Institute - CTRC; University of North Carolina at Chapel Hill

    Chapel Hill, North Carolina, 27599, United States

  • Penn Prevention Research Unit

    Philadelphia, Pennsylvania, 19104, United States

  • Ponce de Leon Center Clinical Research Site

    Atlanta, Georgia, 30303, United States

  • Rutgers New Jesey Medical School - Clinical Research Center

    Newark, New Jersey, 07103, United States

  • UAB, 1917 Research Clinic

    Birmingham, Alabama, 35222, United States

  • UCSD Antiviral Research Center (AVRC)

    San Diego, California, 92103, United States

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