Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Efavirenz/lamivudine/tenofovir disoproxil fumarate is a fixed-dose combination antiretroviral therapy developed by Quality Chemical Industries for the treatment of HIV-1 infection. It consists of three active ingredients: efavirenz (400 mg), a non-nucleoside reverse transcriptase inhibitor (NNRTI); lamivudine (300 mg), a nucleoside reverse transcriptase inhibitor (NRTI); and tenofovir disoproxil fumarate (300 mg), a nucleotide reverse transcriptase inhibitor (NRTI). Efavirenz acts by allosterically inhibiting the HIV reverse transcriptase enzyme, while lamivudine and tenofovir act as competitive inhibitors that cause DNA chain termination. This combination is administered as a single oral tablet once daily, typically at bedtime to mitigate nervous system side effects. It is approved for use in adults and pediatric patients weighing at least 35 kg.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on efavirenz + lamivudine + tenofovir disoproxil fumarate.