Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Doravirine + emtricitabine + tenofovir disoproxil fumarate is an oral fixed-dose combination antiretroviral medication used as a complete regimen for the treatment of HIV-1 infection in adults and pediatric patients weighing at least 35 kg. The combination acts by lowering the levels of HIV in the blood and boosting immune function, but does not cure or prevent HIV or AIDS. - Doravirine is a **non-nucleoside reverse transcriptase inhibitor (NNRTI)**, blocking HIV reverse transcriptase by binding non-competitively, thereby preventing viral replication. - Emtricitabine and tenofovir disoproxil fumarate are **nucleoside analogue reverse transcriptase inhibitors (NRTI)**; they are incorporated into viral DNA by reverse transcriptase and act as chain terminators, blocking viral DNA synthesis. This regimen is approved for treatment-naive patients or as a switch for virologically suppressed patients meeting clinical criteria. The principal developer and manufacturer is Merck Sharp & Dohme. Adverse effects may include renal toxicity and exacerbation of hepatitis B if discontinued in co-infected patients[2][3][4][5][6].
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 doravirine + emtricitabine + tenofovir disoproxil fumarate.