Two injections every six months after starter dosing
The official patient site describes one office visit every six months after the day-1 and day-2 starter sequence is completed.
Plan for both required initiation days: the first day includes professional injections and oral tablets, and the next day includes oral tablets. Confirm that both tablet doses can be obtained before starting. Continuation injections are every 26 weeks, with a two-week window on either side, and HIV testing is required before each injection. Tell the team about travel and supply problems before the date is missed. The label includes prescribed weekly oral bridging for some delays, up to its defined duration; it is not a general self-directed weekly PrEP replacement. A gap longer than 28 weeks without the required oral bridge can require repeating initiation after HIV reassessment. Contact the prescriber rather than guessing from a calendar or residual drug levels. Keep the long-tail testing and alternative-prevention plan if you stop.
Call the prescriber before the 26-week target when possible and provide the last injection date and all bridging tablets taken. If a delay exceeds the two-week allowance, a prescribed oral bridge or a different restart may be needed. The label's pathway after more than 28 weeks without oral bridging includes HIV reassessment and repeating initiation. Do not replace that decision with a self-designed weekly tablet regimen. If a qualifying HIV exposure has occurred within 72 hours during uncertain protection, seek urgent PEP assessment. Book the next injection, testing and any required initiation tablets as a complete plan.
Yeztugo is lenacapavir for prevention of sexually acquired HIV-1 in people who do not have HIV. Treatment starts with injections and tablets, then continues with injections about every six months. It can suit someone who prefers fewer medication visits, provided testing and follow-up remain reliable. Twice-yearly medication does not mean twice-yearly attention to every health concern: a new exposure, symptoms, STI screening or a medication change can require contact sooner.
The approved PrEP indication is for adults and adolescents weighing at least 35 kg who are at risk of acquiring HIV through sex. HIV-negative status must be established. Recent exposure, acute viral symptoms, past PrEP/PEP, pregnancy or breastfeeding and all current medicines belong in the evaluation. HIV testing is required before starting and before each injection. A positive or unknown HIV status prevents use as PrEP.
At initiation, a negative antigen/antibody test is confirmed with HIV RNA testing, even if RNA returns after treatment starts. Before continuation, a negative rapid antigen/antibody test requires confirmation with a more sensitive assay. The clinician determines the complete testing approach and reviews symptoms and any ambiguous results.
Provide every prescription, over-the-counter medicine and supplement. Some strong or moderate CYP3A inducers require additional clinician-directed dosing under the August 2026 label; other starting combinations have no recommended regimen. Your prescriber must review the actual medicines and sequence.
The labeled start includes two subcutaneous injections and oral tablets on the first day, followed by oral tablets the next day. Those tablets are part of required initiation, not an optional tolerability trial. A trained professional administers the injections.
Continuation injections are scheduled every 26 weeks with a two-week allowance on either side. Agree on HIV testing, STI screening and what to do before travel or an access delay.
Bring previous HIV and STI results, your current prevention regimen, last injection date if applicable and insurance information. Ask how the next-day tablets will be obtained and how to contact the team if you cannot take them. Confirm medication receipt and testing arrangements before an administration visit. The label describes abdominal injections and an alternative thigh site; the administrator chooses an appropriate site using the current instructions.
The boxed warning concerns resistance if Yeztugo is used during undetected HIV. Report possible acute HIV symptoms immediately rather than waiting for a routine dose. Injection pain, swelling or nodules can occur; some nodules last a long time. Seek urgent care for severe allergic symptoms or a rapidly worsening injection-site reaction. Lenacapavir can affect other medicines long after the last injection, so tell future prescribers when you received it.
Call before an injection is overdue. An authorized oral bridge may be used for some planned delays, but the tablets are not a patient-designed substitute for injections. Longer gaps without bridging can require repeating initiation after reassessment. After stopping, residual drug may remain for 12 months or longer. Your clinician plans ongoing HIV testing and alternative prevention while levels decline.
Ask separately about tablet coverage, injectable medication coverage, laboratory testing and administration charges. The supply may require authorization and shipment to an administration site. Assistance programs have eligibility rules and do not prove that a particular clinic or insurer participates. Keep a written transition plan while these steps are completed; confirm actual availability before traveling to a listed location.
Yeztugo is lenacapavir for prevention of sexually acquired HIV-1 in people who do not have HIV. Treatment starts with injections and tablets, then continues with injections about every six months. It can suit someone who prefers fewer medication visits, provided testing and follow-up remain reliable. Twice-yearly medication does not mean twice-yearly attention to every health concern: a new exposure, symptoms, STI screening or a medication change can require contact sooner.
The approved PrEP indication is for adults and adolescents weighing at least 35 kg who are at risk of acquiring HIV through sex. HIV-negative status must be established. Recent exposure, acute viral symptoms, past PrEP/PEP, pregnancy or breastfeeding and all current medicines belong in the evaluation. HIV testing is required before starting and before each injection. A positive or unknown HIV status prevents use as PrEP.
At initiation, a negative antigen/antibody test is confirmed with HIV RNA testing, even if RNA returns after treatment starts. Before continuation, a negative rapid antigen/antibody test requires confirmation with a more sensitive assay. The clinician determines the complete testing approach and reviews symptoms and any ambiguous results.
Provide every prescription, over-the-counter medicine and supplement. Some strong or moderate CYP3A inducers require additional clinician-directed dosing under the August 2026 label; other starting combinations have no recommended regimen. Your prescriber must review the actual medicines and sequence.
The labeled start includes two subcutaneous injections and oral tablets on the first day, followed by oral tablets the next day. Those tablets are part of required initiation, not an optional tolerability trial. A trained professional administers the injections.
Continuation injections are scheduled every 26 weeks with a two-week allowance on either side. Agree on HIV testing, STI screening and what to do before travel or an access delay.
YEZTUGO is not available at retail pharmacies. The prescribing office may have it or arrange it through a specialty pharmacy. Confirm the actual administration address, shipment receipt, HIV testing and starter tablets with the team before traveling. The injections are administered by a healthcare professional. This is not a retail self-injection kit.
No. Oral tablets on both initiation days are part of the labeled regimen. Contact your clinician immediately if the second-day tablets are unavailable, missed or vomited; do not improvise replacement doses.
The exact plan must be checked for both formulations, the dispensing route and administration site. Also ask about visits and laboratory charges. Another person’s approval or copay is not a reliable estimate of yours.
A clinician can compare options and make a transition plan based on HIV results, last doses, exposure and interactions. Keep the existing prevention plan until you receive explicit instructions; changing products without coordination can leave a gap.
Book a Yeztugo first visit Call (917) 310-3371
Eligibility, testing and what to bring · Side effects and safety · Starter doses and return visits
The official patient site describes one office visit every six months after the day-1 and day-2 starter sequence is completed.
On day 1, the patient receives two injections and two oral tablets. On day 2, two more oral tablets are taken at home before the every-six-months continuation cadence begins.
Official materials state that YEZTUGO is injected by a healthcare professional in a medical setting rather than obtained from a retail pharmacy.
YEZTUGO is not a retail-pharmacy medication. Official patient materials say the provider may carry it in office or obtain it another way, such as through a specialty pharmacy, and delivery can take about 30 days once a prescription is ordered.
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30-07 36th Ave, Astoria, NY 11106
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Long Island
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Manhattan
259 1st Ave, New York, NY 10003
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Brooklyn
308 Graham Ave, Brooklyn, NY 11211
A Brooklyn clinic that can help patients ask about YEZTUGO availability, coverage support, and PrEP follow-up, serving patients in Williamsburg, Greenpoint, Bushwick, and nearby Brooklyn neighborhoods.
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