Skip to content
Clinical Trials – home

Rasmussen encephalitis Trials in Disease

1 / 1 trials open to patients1 country

In short

Currently, there is one ongoing clinical trial investigating a novel stem cell-based treatment for children and adolescents with Rasmussen encephalitis, a rare inflammatory brain disease. This trial is being conducted in Spain and focuses on evaluating the safety of repeated intra-arterial infusion of mesenchymal stem cells in patients whose epilepsy does not respond to standard treatments.

Clinical trial locations

Study on the Safety of Repeated Intra-Arterial Infusion of Mesenchymal Stem Cells for Children and Adolescents with Refractory Epilepsy

This clinical trial is investigating a new treatment approach for children and adolescents with refractory epilepsy, including those with Rasmussen encephalitis. Refractory epilepsy means the condition does not respond well to standard treatments, making it particularly challenging to manage.

Main inclusion criteria:

  • Children under 16 years of age
  • Epilepsy caused by immune system problems that does not respond to usual anti-seizure medications and standard immune therapies
  • Patients who have had epilepsy surgery due to Rasmussen encephalitis are specifically included
  • Ability to undergo necessary medical tests including heart scans, electrical activity tests, imaging tests, and brain function assessments
  • Written agreement (informed consent) from the patient or legal guardian to participate in the study

Main exclusion criteria:

  • Patients with epilepsy that is not related to the immune system
  • Those with other serious health conditions that might interfere with the study
  • Patients currently participating in another clinical trial
  • Recent infection or illness that could affect study results
  • Pregnant or breastfeeding patients
  • History of allergic reactions to similar treatments
  • Inability to follow study procedures or attend required visits

Trial focus and goal: The primary purpose of this study is to evaluate the safety and tolerability of a treatment called AloCelyvir. The trial monitors patients closely for any side effects, particularly within the first 28 days after treatment. The study also observes any changes in epilepsy symptoms and overall condition. The trial involves several stages, starting with a comprehensive initial assessment, followed by obtaining informed consent, then the actual treatment administration, ongoing monitoring, and finally a complete evaluation at the end of the trial, which is expected to conclude by December 31, 2027.

Investigational treatment: The treatment being tested uses mesenchymal stem cells, which are special cells taken from the patient's own body (autologous cells). These cells are modified in a laboratory setting and then infused directly into the arteries through a procedure called intra-arterial infusion. The treatment is given in repeated doses according to the trial protocol. These stem cells are believed to work by modulating the immune system and promoting repair of damaged brain tissue, potentially reducing inflammation and seizure activity. This represents a novel approach to treating refractory epilepsy and Rasmussen encephalitis, offering hope where conventional treatments have not been successful.

Summary

There is currently one active clinical trial available for patients with Rasmussen encephalitis, located in Spain. This Phase I trial represents an innovative approach to treating this rare and challenging condition by using stem cell therapy. The trial is specifically designed for children and adolescents whose epilepsy has not responded to conventional treatments, including those who have already undergone epilepsy surgery.

The focus on stem cell-based therapy reflects growing interest in cell-based treatments for neurological conditions. The trial's emphasis on safety evaluation is appropriate for this early-phase study, as this type of treatment is still experimental. Patients interested in participating should be aware that the trial requires the ability to undergo various medical tests and attend regular follow-up visits through the end of 2027.

This guide is here to help you understand the condition. It does not replace a conversation with your doctor, who knows your situation best.

Clinical trials for Rasmussen encephalitis

Recruiting trials first

See all 1 trials →
Quick filters

1 clinical trial in this condition

Countries:SpainSpain
  • Participants:0–17 years
  • Substances:Allogenic Bone Marrow-Derived Mesenchymal Stem Cells Transduced With Icovir-5, Ex Vivo Expanded
  • Sponsor:Fundacion Para La Investigacion Biomedica Del Hospital Universitario La Princesa
See all 1 trials →filters applied: condition = Rasmussen encephalitis

Related conditions in the same therapeutic area

Back to all diseases
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

© 2026 Clinical Trials EU – European Clinical Trials Information Network

GDPR compliance, ISO 9001 and ISO 27001 certified (LL-C Certification)

On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).