Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Mafusol is an approved, intravenously administered crystalloid infusion solution with antihypoxic, rehydrating, and detoxifying properties. Developed by the Russian Research Institute of Hematology and Transfusiology and manufactured by Firm Medpolymer and Biosintez, Mafusol is a combination of sodium fumarate, sodium chloride, potassium chloride, and magnesium chloride. The primary active component, sodium fumarate, acts as an antihypoxic agent by entering the tricarboxylic acid (Krebs) cycle, where it is metabolized to support ATP synthesis and maintain cellular energy production under conditions of oxygen deficiency. Mafusol is indicated for the treatment of hypovolemic and hypoxic states, including acute blood loss, shock (hemorrhagic, burn, traumatic, and operative), severe intoxication (such as peritonitis or sepsis), and ischemic stroke. It is also used as a perfusion component to fill the cardiopulmonary bypass circuit during cardiac surgery.
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 Mafusol.