There is hope for patients suffering from an energy metabolism disease. The company Khondrion, a spin-off from the Radboudumc university hospital in Nijmegen, the Netherlands, has been working in recent years to develop a new medicine for these rare diseases. A preliminary study in children started this month This caused Jan Smeitink, professor of Mitochondrial Medicine at the Radboudumc in Nijmegen, a lot of frustration: he diagnosed and treated his patients as well as he could, except that there is no medication available.

Smeitink is a pediatrician who specializes in mitochondrial diseases, also known as energy metabolism disorders. Mitochondria are found in almost every cell in the human body, where they convert sugars and fats into energy. You can see these as a kind of energy factory or battery inside the body. Mitochondria malfunctions in patients who have an energy metabolic disorder means that their cells do. not receive enough energy and harmful substances are released that eventually cause cells to die. This leads to a variety of problems such as muscle weakness, fatigue, developmental or growth retardation, problems with vision or hearing, and heart problems. The first symptoms are often seen in children, although sometimes the disease only manifests itself in adulthood.

This image has an empty alt attribute; its file name is Jan-Smeitink-portret-669x1004.jpg
Jan Smeitink

There are more than 300 known genes where faults lead to mitochondrial diseases; all of which are rare or extremely rare. Some mitochondrial diseases are so severe that children die of them at an early age. The course of disease can also be more mild, with a longer life expectancy.

Subscribe to IO on Telegram!

Want to be inspired 365 days per year? Here’s the opportunity. We offer you one "origin of innovation" a day in a compact Telegram message. Seven days a week, delivered around 8 p.m. CET. Straight from our newsroom. Subscribe here, it's free!

Subscribe!

Repairing damage

Is it possible to repair these broken energy factories or at least prevent them from causing more damage in the body, in some cases even to the point of death? Smeitink resolved to seek the answer to that question himself.

The company Khondrion started its work activities in 2012. Initially, Smeitink did this alongside his work as a pediatrician and professor at the Radboudumc. During his search for a medicine, Smeitink decided to focus on the MELAS spectrum syndrome. Malfunctioning mitochondria in these patients can lead to cognitive problems (e.g., difficulty concentrating or being able to plan and make decisions), stroke-like seizures, deafness, muscle weakness, fatigue, and diabetes. The symptoms usually develop in late childhood or early adulthood. About 50,000 patients worldwide suffer from this form of mitochondrial disease. By comparison, Parkinson’s affects about 7 million patients worldwide.

Children with an energy metabolism disorder also have a lot to gain through this.” Jan Smeitink

Khondrion tested a substantial series of new chemical compounds and their effects on mitochondria. You cannot prevent or eliminate faulty mitochondria, but you can potentially limit the harmful effects. “We received a grant from ZonMw in order to research this, and we are also supported by various charitable foundations. This enabled us to get started very quickly,” says Smeitink. Sonlicromanol emerged as the most promising of a number of candidate molecules. The results in the laboratory in cell and animal models also proved to be very promising.

Prestigious grant

“Yet after this study, it was extremely difficult to get funds for any further research, even though we really need it,” Smeitink says. “Eventually, we managed to secure a prestigious European Horizon 2020 grant and a grant from the Economic Fund for Regional Development (ERDF). But we have to be seriously economical with the funds that we have. As a result, research is not progressing as fast as we would like.”

Yet significant and important steps are now being taken. Smeitink currently works full-time as CEO of Khondrion. “It was not possible to combine it with clinical duties at the hospital. The cooperation between the Radboudumc and our company is excellent. The hospital conducts the trials with sonlicromanol that has been developed by Khondrion and together we work on various research projects.”

Clinical research

The drug has now been tested in humans and its results published in professional medical papers. “First in healthy subjects, then in a small group of patients. We are looking forward to its potential efficacy on MELAS spectrum syndrome patients as well as on other mitochondrial diseases.”

Khondrion hopes to complete an international study this year – the phase 2b study – in adult patients in the Netherlands, Germany and England. They plan to study the drug’s effectiveness in a larger group of patients. The drug appears to improve patients’ cognitive function, making them more alert, for ont thing. But Smeitink also hopes for positive results on other bodily systems, such as motor function.

Trial in children

A study was recently started on children living with mitochondrial diseases. This is something that Smeitink considers very important because there is plenty of room for improvement here. The children participating in the study are affected by movement disorders and spasticity, among other things. Some of the children with a metabolic disease die before they reach the age of ten. Smeitink: “We cannot cure the disease. But we hope that the earlier we start treating it, the better the effect.”

If all goes well, Smeitink hopes that the drug will be approved for the market in three years, by which time it is hoped that a large proportion of patients can be helped.

The drug sonlicromanol has now received an orphan drug status rating from the European Medicines Agency (EMA) and the FDA. Once this is done, the research will be able to count on various incentive schemes for this type of drug. This makes it easier when it comes to applying for funding.

Also interesting: New medicine to treat Parkinson’s disease one step closer

Support us!

Innovation Origins is an independent news platform that has an unconventional revenue model. We are sponsored by companies that support our mission: to spread the story of innovation. Read more.

At Innovation Origins, you can always read our articles for free. We want to keep it that way. Have you enjoyed our articles so much that you want support our mission? Then use the button below:

Doneer

Personal Info

About the author

Author profile picture