A cocktail of drugs may work against a whole family of viruses

Enteroviruses are a group of viruses that cause everything from the common cold to meningitis, polio, type 1 diabetes, and much more. Over 100 different types have been described by researchers, and millions of people are infected each year.

“Enteroviruses pose a significant global health problem,” said Erlend Ravlo, a PhD research fellow at the Norwegian University of Science and Technology (NTNU’s) Department of Clinical and Molecular Medicine.

It may therefore sound a bit strange that we still haven’t developed an approved general treatment or a vaccine for this group of viruses.

One explanation may be that infected patients usually recover well without medication. Sometimes, however, things can really take a turn for the worse, especially with children, which is why it is important to find a treatment method that can work against multiple enteroviruses.

Medication cocktail stops replication

Researchers are on the trail of a solution. Viruses replicate by making copies of themselves within the cells they infect, which makes for a good target where an intervention can be made.

“We have identified a combination of drugs that appears to prevent enteroviruses from replicating,” said Aleksandr Ianevski at the Department of Clinical and Molecular Medicine.

The combination of drugs has not yet been tested on humans, but trials have been conducted on human cells and cultures of mini-organs in the laboratory – and the results are positive.

The work on enteroviruses has involved dozens of researchers in Norway and other European countries.  The research results have now been published in two research articles.

The corresponding authors are professors Denis Kainov and Magnar Bjørås, both from the Department of Clinical and Molecular Medicine.

Can be taken orally

One combination consists of three drugs already known to health professionals: pleconaril, AG7404 and mindeudesivir. This combination of medicine can be taken orally.

These drugs have already been individually tested on humans, and safe doses of the combination appear to be effective against enteroviruses in cells and cultures of mini-organs.

“In addition, the combination does not alter glucose or insulin levels when tested on pancreatic cells in the laboratory,” said Kainov.

This is good news for people who have or fear developing diabetes.

The researchers have also tested the combination on mini-organs that simulate hearts, and it does not appear to alter the heart rate, which is, of course, also important.

“This cocktail of medicines is really promising,” said Bjørås.

Tested several combinations

Finding the optimal combination of drugs took time. The NTNU researchers tried other possible treatments by testing several different mixtures.

“To find an effective treatment, we analyzed the toxicity and effectiveness of 12 known agents that can work against a wide range of enteroviruses. We tested them both individually and in combination, and against different viruses in cell cultures,” explained Kainov.

A promising combination is pleconaril, rupintrivir and remdesivir, which was effective against several viruses in lung cells and intestinal organoids. However, since rupintrivir and remdesivir cannot be taken as a single combined pill, the researchers replaced them with AG740 4 and mindeudesivir. The new combination is still effective, while being more practical because it can be taken as a single pill.

“Our studies show great potential for finding broad-spectrum treatment methods against enteroviruses,” said Kainov.

Bjørås emphasized that more studies are needed before we can confirm that these combinations of drugs are also effective in patients. These studies must involve several different enteroviruses, both in the laboratory and in clinical trials on humans.

Reference:References:Ravlo, E., Ianevski, A., Schjølberg, JO. et al. Synergistic combination of orally available safe-in-man pleconaril, AG7404, and mindeudesivir inhibits enterovirus infections in human cell and organoid cultures. Cell. Mol. Life Sci. 82, 57 (2025). https://doi.org/10.1007/s00018-025-05581-4