Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lumet HS is a fixed-dose combination antimalarial drug developed and manufactured by Quality Chemicals Industries Limited (QCIL) in Uganda. It is a higher-dose formulation containing 80 mg of artemether and 480 mg of lumefantrine in a single oral tablet, designed for adults and children weighing over 35 kg. Artemether, an artemisinin derivative, provides a rapid onset of action by interfering with heme metabolism and damaging parasite biomolecules, leading to quick symptomatic relief. Lumefantrine acts as a long-acting blood schizonticide that clears residual parasites to prevent recrudescence. This combination therapy is indicated for the treatment of uncomplicated malaria caused by *Plasmodium falciparum* and other *Plasmodium* species, and is particularly effective against chloroquine-resistant strains.
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 Lumet HS.