Fondazione I.R.C.C.S. Istituto Neurologico Besta
Verified
Milan, Italy
Rare diseases
Investigational molecules
Locations
A plain-language summary of the goals, design and what participants do
This study focuses on patients with Glioblastoma Multiforme, an aggressive type of brain cancer. The study evaluates the long-term safety of a treatment called Temferon, which was previously given to patients. Temferon is a special type of therapy that uses the patient's own blood stem cells that have been modified to carry a specific gene.
The treatment involves hematopoietic stem cells (blood-forming cells) that are collected from the patient's own body. These cells are modified in a laboratory to include a gene that produces interferon alpha-2, a substance that can help fight cancer. The modified cells are then given back to the patient through an intravenous infusion (through a vein).
The main purpose of this follow-up study is to monitor the long-term safety of Temferon treatment. The study will specifically look at whether the modified cells could potentially cause any blood disorders or other health issues over time. Patients who have previously received Temferon treatment will be monitored for several years to ensure their safety and to track how well the treatment continues to work.
The trial runs in 5 steps – from screening to follow-up. Each step says what happens and what the team monitors.
7 criteria
15 criteria
Tell us about your condition – we search every trial in Europe and connect you with the right site.
We usually reply within a few days
All sites with verified contact details – recruitment status may not be available; ask directly
Milan, Italy
Milan, Italy
Where you can join this trial
Countries are shaded by recruitment status. Click a recruiting country to ask about joining there.
RecruitingJoining a clinical trial can seem overwhelming. We guide you step by step, so you know exactly what to expect and how we support you through the process.
is a specialized cell therapy that uses the patient's own blood stem cells (CD34+ cells). These cells are modified in a laboratory using a special virus carrier (lentiviral vector) to make them produce interferon-α2, a protein that helps fight cancer. The modified cells are then given back to the patient to help treat glioblastoma multiforme, a type of brain cancer. This therapy aims to deliver targeted treatment directly to the tumor area.
is a natural protein that the body produces to fight diseases. In this treatment, it is produced by the modified cells to help combat the brain tumor. It works by boosting the immune system and potentially slowing down tumor growth.
sourced from the EU Clinical Trials Register and site verification
Want to learn more about this trial or check if you can participate?
Tell us about your condition – we search every trial in Europe and connect you with the right site.