Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This drug entry refers to a combination of standard-of-care antimalarial regimens used as a comparator in clinical trials conducted by the University of Oxford, specifically in the context of treating malaria in Afghanistan. The regimen consists of artesunate plus sulphadoxine-pyrimethamine (AS+SP) for the treatment of uncomplicated *Plasmodium falciparum* malaria and chloroquine for the treatment of *Plasmodium vivax* malaria. Artesunate is a rapid-acting artemisinin derivative that generates reactive oxygen species and free radicals to damage parasite proteins and membranes. Sulphadoxine and pyrimethamine are antifolate agents that synergistically inhibit dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR), respectively, disrupting the parasite's DNA synthesis. Chloroquine acts by interfering with the parasite's ability to detoxify heme into hemozoin within its food vacuole, leading to the accumulation of toxic heme. This specific combination of regimens was evaluated in a Phase 3 trial to compare its efficacy and safety against dihydroartemisinin-piperaquine (Artekin) to support the simplification of national malaria treatment protocols.
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 artesunate + sulphadoxine + pyrimethamine + chloroquine.