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The drug repurposing of the antiparasitic drug Ivermectin (IVM) for the treatment of COVID-19 (SARS-CoV-2) has been explored in several studies. Ivermectin blocks the nuclear import pathway mediated by host protein IMPα/β1, inhibiting the entry of viral proteins into the cell nucleus, thereby enhancing the host's antiviral response and belongs to a host-directed drug. Additionally, molecular docking and kinetic simulations have shown that Ivermectin can stably bind to multiple SARS-CoV-2 targets (such as Nsp9, protease 3CLpro, spike protein RBD), demonstrating multi-target antiviral potential. Among them, Nsp9 and Spike RBD show the strongest binding force and stability.
A total of 80 clinical trials have been launched globally to evaluate the efficacy of Ivermectin on COVID-19 (such as NCT04510233, NCT04425850), and some studies have shown that it can alleviate symptoms, reduce inflammation levels, and lower mortality rates.
Overall, as a multi-target and mechanism-defined drug, Ivermectin is expected to be a supplementary option in the treatment strategy for COVID-19.
Fig. 1 Mechanism of action for Ivermectin against SARS-CoV-2. (Patil V M.; et al. 2022)
References
Patel H et al. addressed the treatment challenges of rosacea and developed and optimized an Ivermectin-loaded niosomal gel. Niosomes were prepared using the ether injection method, and the formulation was optimized through a 32-factor experimental design. The gel was evaluated for pH, viscosity, and in vitro release performance. The results showed that this gel had high drug stability, controlled release performance, and release rate, which were superior to commercially available Ivermectin products, and could improve drug bioavailability and efficacy.
Fig. 2 Ivermectin-loaded niosomal gel for the treatment of rosacea. (Patel H.; et al. 2025)
References
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