Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lamivudine + raltegravir is a dual antiretroviral therapy (ART) regimen investigated for the maintenance of virological suppression in patients living with HIV-1. This combination consists of lamivudine (300 mg), a nucleoside reverse transcriptase inhibitor (NRTI), and raltegravir (1200 mg), an integrase strand transfer inhibitor (INSTI). The regimen is primarily studied as a simplification strategy for patients who are already virologically suppressed but seek to reduce drug-related toxicity, pill burden, or potential drug-drug interactions associated with standard triple-therapy regimens. By utilizing a high-dose, once-daily raltegravir formulation alongside lamivudine, the therapy aims to provide a potent, well-tolerated alternative for long-term HIV management. The RALAM-II Phase 3b trial, led by Judit Pich at the Hospital Clínic de Barcelona, specifically evaluates this dual therapy in patients experiencing inconvenience or toxicity with their current regimens.
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 lamivudine + raltegravir.