Truvada (emtricitabine / tenofovir disoproxil) vs Vocabria (cabotegravir)

Truvada (emtricitabine / tenofovir disoproxil) vs Vocabria (cabotegravir)

Truvada (emtricitabine/tenofovir disoproxil) is an oral medication taken daily for pre-exposure prophylaxis (PrEP) to reduce the risk of HIV infection, and it's also used in combination with other medications to treat HIV. Vocabria (cabotegravir), on the other hand, is an injectable medication administered initially as an oral lead-in to assess tolerability, followed by intramuscular injections every two months for PrEP, offering an alternative to daily pill-taking. When deciding between the two, patients should consider factors such as their preference for daily versus less frequent dosing, potential side effects, kidney function, and their overall adherence to treatment regimens, in consultation with their healthcare provider.

Difference between Truvada and Vocabria

Metric Truvada (emtricitabine / tenofovir disoproxil) Vocabria (cabotegravir)
Generic name Emtricitabine / Tenofovir disoproxil Cabotegravir
Indications HIV-1 infection prevention and treatment HIV-1 infection treatment (as part of a combination therapy)
Mechanism of action Reverse transcriptase inhibitors Integrase strand transfer inhibitor (INSTI)
Brand names Truvada Vocabria
Administrative route Oral Oral, Injectable (long-acting formulation)
Side effects Nausea, diarrhea, headache, fatigue, dizziness Fever, fatigue, headache, muscle pains, injection site reactions
Contraindications Patients with hypersensitivity to the active substances or any of the excipients Patients with hypersensitivity to the active substance or any of the excipients
Drug class Nucleoside reverse transcriptase inhibitors (NRTIs) Integrase strand transfer inhibitor (INSTI)
Manufacturer Gilead Sciences ViiV Healthcare

Efficacy

Efficacy of Truvada in HIV/AIDS Prevention and Treatment

Truvada, a combination of emtricitabine and tenofovir disoproxil, is a medication that has been widely used in the treatment and prevention of HIV/AIDS. In the context of treatment, Truvada is part of antiretroviral therapy (ART) regimens for individuals who are living with HIV. It works by inhibiting the action of reverse transcriptase, an enzyme crucial for the replication of HIV. Clinical trials and studies have consistently shown that Truvada, when used in combination with other antiretroviral agents, is highly effective in reducing viral load to undetectable levels and in improving CD4 cell counts, which are key indicators of immune system health.

For HIV prevention, Truvada is used as pre-exposure prophylaxis (PrEP). It is intended for individuals who are at high risk of acquiring HIV, such as those with an HIV-positive sexual partner. Studies have demonstrated that when taken consistently, Truvada can reduce the risk of sexually acquired HIV infection by a significant margin. The US Centers for Disease Control and Prevention (CDC) supports its use as an effective preventive measure, alongside other risk-reduction strategies.

Efficacy of Vocabria (Cabotegravir) in HIV/AIDS Prevention

Vocabria, which contains the active ingredient cabotegravir, is a newer medication that has been evaluated for its efficacy in HIV prevention. Unlike Truvada, which is taken orally, Vocabria is administered as an intramuscular injection. It is used as part of a regimen for pre-exposure prophylaxis (PrEP) and is designed for individuals who are at risk of HIV but have difficulty adhering to a daily oral medication regimen. Clinical trials have shown that cabotegravir injections, given every two months, are highly effective in reducing the risk of HIV acquisition in men who have sex with men (MSM) and transgender women who have sex with men, populations that are at high risk for HIV.

One of the pivotal trials for Vocabria, the HPTN 083 study, compared the efficacy of long-acting injectable cabotegravir to daily oral Truvada for PrEP. The results indicated that cabotegravir was superior to Truvada in preventing HIV acquisition in the study population. The trial demonstrated a 66% reduction in HIV incidence among participants receiving cabotegravir compared to those receiving Truvada. This finding has positioned Vocabria as a promising alternative for PrEP, offering a less frequent dosing schedule that may improve adherence and overall prevention outcomes.

Regulatory Agency Approvals

Truvada
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
Vocabria
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia

Access Truvada or Vocabria today

If Truvada or Vocabria are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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