Harvard University
Cambridge, United States
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Glioblastoma is the most common and most aggressive primary brain cancer in adults, starting in the brain's supporting glial cells.
Not yet. Glioblastoma is treatable, but not yet curable: treatment can slow it down, ease symptoms and help people live longer. Six treatments are approved for glioblastoma by the US FDA: temozolomide (about this drug · open trials), lomustine (about this drug · open trials), carmustine (as a drip and as an implanted wafer) (about this drug · open trials), bevacizumab (about this drug · open trials) and the Optune tumour treating fields device (open trials). Researchers worldwide are working to do better.
For most adults who are fit enough, the European EANO guideline (2021) recommends surgery to remove as much of the tumour as is safe, then radiotherapy given together with temozolomide chemotherapy, followed by six cycles of temozolomide. Tumour treating fields, a wearable device, are approved in the US for use with temozolomide. When the tumour comes back, doctors may consider lomustine, bevacizumab, more surgery or radiotherapy, or a clinical trial.
As of November 2026, our database lists 248 different investigational treatments in recruiting or ongoing glioblastoma trials from Phase 1 to Phase 3. They include:
Several hundred laboratory and animal studies published in the past year explore further ideas. Most of these need years of work before they can be tested in people.
Eleven treatments have reached Phase 3, the last stage before a request for approval. Among the new medicines and devices furthest along:
Other Phase 3 trials test pembrolizumab with tumour treating fields and temozolomide (EF-41, NCT06556563), the SonoCloud-9 implant with carboplatin (NCT05902169) (open trials) and adding lomustine to temozolomide (NCT06419946). The GBM AGILE platform trial (NCT03970447) tests several drugs side by side.
Trial teams estimate that main data collection will finish around the end of 2026 for NaviFUS, mid-2027 for TLX101, the end of 2027 for niraparib and 2029 for EF-41. These dates are estimates and often move. A positive result would still need review by regulators before a treatment becomes widely available.
Machine summary of published research · sources and dates below · 2026-11-03
Written from: FDA: Temodar (temozolomide), NDA 021029 – Drugs@FDA · FDA: Gliadel (carmustine wafer), NDA 020637 – Drugs@FDA · FDA: BiCNU (carmustine) label, NDA 017422 (2017) · DailyMed: Gleostine (lomustine) label · FDA: Avastin (bevacizumab), BLA 125085 – Drugs@FDA · FDA: Optune (NovoTTF-100A), premarket approval P100034 · EANO: EANO guidelines on the diagnosis and treatment of diffuse gliomas of adulthood (Weller et al., Nat Rev Clin Oncol 2021) · ClinicalTrials.gov: trial records (the NCT numbers in the text) · read on 2026-11-03
Estimated from 429 therapy-related publications from the last 12 months. These are studies, not separate treatments.
Estimated from 321 therapy-related publications from the last 12 months. These are studies, not separate treatments.
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Here you will find questions you can ask, help with difficult talks, organisations for carers and your relative's rights.
Questions for your relative's doctor
You do not need the right words. Ask what your relative wants to know, and let them set the pace. These pages can help.
Looking after someone is work too. These organisations help carers, and the list further down this page shows helplines by country.
A doctor can share information and a relative can act only with the patient's consent or a legal authority. It is easier to arrange this early.
Children are often treated differently from adults, in specialist centres. Here is where to start.
These European networks connect paediatric cancer centres and families.
Parents often receive offers of paid treatment. Please go through this list before you pay for anything.
You can share or print these pages for your members. They are free and need no account.
The trial team decides who can take part; your doctor can help you ask.
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Results, new trials and publications, newest first. Every item links to its source.
Results and new studies, newest first, in plain words.
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New and changed trials of the last 30 days, without an account and without tracking.
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Quantitative imaging in medicine and surgery
PubMed · PMID 42999586Pick up to 5 questions for your situation, then print them or take them on your phone.
Choose questionsIf the treatment has stopped working, or you were told there are no more options, here is what you can ask and where you can look next.
Do not stop or put off treatment without talking to your doctor.
Many trials look specifically for people who have already had treatment. Registries mark these with words like "previously treated", "refractory" or "relapsed". The trial team decides who can take part.
A phase 1 trial mainly tests whether a new medicine is safe and which dose can be given. It is not built to show that the medicine works.
In cancer, older figures show that fewer than 1 in 20 people in a phase 1 trial respond. Many people expect far more, so ask openly: what can I expect, and what will it mean for my daily life?
Some medicines not yet approved can be given outside a trial when there is no other option. This does not exist for every medicine or in every country. Your doctor makes the request, and the authority or the manufacturer decides.
Asking for a second opinion is normal and does not mean you distrust your doctor. Take your results and a list of your treatments with you. For rare diseases, your doctor can also ask a European Reference Network.
This is care for symptoms and quality of life, and you can have it alongside cancer treatment. It does not mean anyone has given up on you. In a randomised trial in advanced lung cancer, palliative care from early on improved quality of life.
In this situation many people receive offers of paid treatment. Go through this list before you pay for anything.
You can talk to someone. In Hungary and in the UK, 116 123 is a free line for emotional support, day and night. The list on this page shows helplines in other countries.
Not medical advice. Talk to your care team before you change anything in your treatment.
Helplines, patient groups and support services for you and your family.
Select your country to see the organisations there, starting with the ones closest to you.
European network of paediatric cancer centres with virtual tumour boards and a section for patients and families.
Visit site: ERN PaedCan – ERN for paediatric oncologyEuropean network of expert centres for rare adult cancers, including brain tumours; your doctor can bring your case to it.
Visit site: EURACAN – ERN for rare adult solid cancersUmbrella of European cancer patient groups, with a patient toolbox and a legal network for cancer patients.
Visit site: European Cancer Patient Coalition (ECPC)The European Commission's 24 expert networks for rare and complex diseases; your doctor can contact them.
Visit site: European Reference Networks (European Commission)Alliance of over 1,000 rare disease patient organisations, with a list of rare disease helplines by country.
Visit site: EURORDIS – Rare Diseases EuropeWorldwide network of brain tumour patient and carer groups, with a free magazine and a clinical trials portal.
Visit site: International Brain Tumour Alliance (IBTA)For anyone who is ill, whatever the disease: patients' rights and legal aid, crisis lines, hospice and palliative care, care in another EU country, and patient organisations' umbrella bodies.
Umbrella of European patient organisations and national patient coalitions.
Visit site: European Patients' Forum (EPF)Global alliance of patient organisations of all diseases, promoting patient-centred healthcare.
Visit site: International Alliance of Patients' OrganizationsFrontlight is not affiliated with these organisations; we list them because they help.
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