Truvada (emtricitabine / tenofovir disoproxil) vs Rukobia (fostemsavir)

Truvada (emtricitabine / tenofovir disoproxil) vs Rukobia (fostemsavir)

Truvada (emtricitabine/tenofovir disoproxil) is primarily used for the treatment and prevention of HIV-1 infection in combination with other antiretroviral agents, and as pre-exposure prophylaxis (PrEP) to reduce the risk of sexually acquired HIV-1 in adults and adolescents. It is generally prescribed for individuals with no or mild HIV treatment experience and has a well-established safety profile. In contrast, Rukobia (fostemsavir) is an attachment inhibitor designed for the treatment of HIV-1 infection in heavily treatment-experienced adults with multidrug-resistant HIV-1 infection failing their current antiretroviral regimen due to resistance, intolerance, or safety considerations, offering a new mechanism of action for those with limited treatment options.

Difference between Truvada and Rukobia

Metric Truvada (emtricitabine / tenofovir disoproxil) Rukobia (fostemsavir)
Generic name Emtricitabine / Tenofovir disoproxil Fostemsavir
Indications HIV-1 infection in combination with other antiretroviral agents Treatment of HIV-1 infection in heavily treatment-experienced adults with multidrug-resistant HIV-1 infection failing their current antiretroviral regimen due to resistance, intolerance, or safety considerations
Mechanism of action Reverse transcriptase inhibitors Attachment inhibitor
Brand names Truvada Rukobia
Administrative route Oral Oral
Side effects Diarrhea, nausea, fatigue, headache, dizziness, depression, insomnia, abnormal dreams, rash Nausea, fatigue, diarrhea, headache, abdominal pain, insomnia
Contraindications Patients with prior hypersensitivity to emtricitabine or tenofovir disoproxil fumarate Patients with previous hypersensitivity reaction to fostemsavir or any component of the product
Drug class Nucleoside Reverse Transcriptase Inhibitors (NRTIs) HIV-1 attachment inhibitor
Manufacturer Gilead Sciences ViiV Healthcare

Efficacy

Efficacy of Truvada for HIV/AIDS Prevention and Treatment

Truvada, a combination of emtricitabine and tenofovir disoproxil fumarate, is a highly effective medication used in the prevention and treatment of HIV/AIDS. As part of antiretroviral therapy (ART) for individuals living with HIV, Truvada works by reducing the amount of virus in the body and helping to boost the immune system. Clinical trials and real-world studies have consistently shown that Truvada, when taken as prescribed, is effective at suppressing viral loads to undetectable levels, which not only improves the health of the individual but also reduces the risk of HIV transmission to others.

For HIV prevention, Truvada is used as pre-exposure prophylaxis (PrEP). In this context, it is highly effective in reducing the risk of HIV infection among at-risk populations, including men who have sex with men, heterosexual couples where one partner is HIV-positive, and intravenous drug users. Studies have demonstrated that when taken consistently, Truvada can reduce the risk of HIV acquisition by up to 92%. However, the efficacy of Truvada as PrEP is closely tied to adherence, with significantly reduced protection in individuals who do not take the medication regularly.

Efficacy of Rukobia for HIV/AIDS Treatment

Rukobia (fostemsavir) is a novel antiretroviral medication approved for the treatment of HIV/AIDS in adults with multidrug-resistant HIV-1 infection who have limited treatment options due to resistance, intolerance, or safety considerations. As a first-in-class HIV-1 attachment inhibitor, Rukobia works by blocking the virus from attaching to and entering the host's immune cells. This mechanism is distinct from other antiretroviral drugs, making Rukobia an important option for patients with heavily treatment-experienced HIV.

The efficacy of Rukobia was demonstrated in a pivotal phase 3 clinical trial, BRIGHTE, which included a cohort of heavily treatment-experienced adults with multidrug-resistant HIV. The results showed that a significant proportion of participants achieved and maintained viral suppression when Rukobia was added to an optimized background therapy. The trial underscored the importance of Rukobia as a therapeutic option for individuals who have exhausted other available treatments and are in need of alternative strategies to manage their HIV infection effectively.

Regulatory Agency Approvals

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

Access Truvada or Rukobia today

If Truvada or Rukobia 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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