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NCT06804655Recrutement en cours

Pharmacoscopy for Patients With Refractory Primary Brain Tumors

Résumé

Advanced technology of ex vivo drug profiling referred to as pharmacoscopy may allow to identify novel drugs for the treatment of glioblastoma and other refractory brain tumors at an individual patient level. This personalized therapeutic approach was developed and validated in pre-clinical glioma models. With the current research proposal, we seek to establish feasibility for a clinical interventional trial for patients with refractory primary brain tumors that is based on pharmacoscopy-guided selection of treatment. The study is supported by an unrestricted grant from Anti Cancer Fund.

Critères d'inclusion

1. Age 18 years or older on day of signing informed consent, female or male. 2. Refractory glioblastoma, isocitrate dehydrogenase (IDH)-mutant astrocytoma or oligodendroglioma, histone-mutant glioma, ependymoma, medulloblastoma, meningioma or other rare primary brain tumor with a histological confirmation according to the WHO classification 2021. Primary tumors can be located at the cerebral or spinal level. Primary brain tumors with metastases outside of the brain may also be considered. 3. Karnofsky performance status of 60 or more 4. Life expectancy \>12 weeks. 5. Limited systemic therapeutic options as per treating physician judgement. The number of previous lines of therapies is not limited. 6. Surgery clinically indicated. A histological confirmation of the diagnosis of a recurrent brain tumor will be required before any treatment can be initiated. 7. Adequate bone marrow, renal and hepatic function 8. Ability to understand the requirements of the study, provide written informed consent and authorization of use and disclosure of protected health information, and agree to abide by the study restrictions and return for the required assessments. 9. Written informed consent for study participation must be signed and dated by the patient and the investigator prior to any study-related intervention.

Critères d'exclusion

1. Inability to undergo brain or spine MRI. 2. Concurrent treatment with other systemic tumor-directed pharmacotherapies. 3. Intent to be treated with radiotherapy. 4. Any investigational antitumor therapy other than those under investigation in this study. 5. Judgment by the investigator that the patient should not participate in the study because the patient is unlikely to comply with study procedures, restrictions and requirements. 6. Intention to become pregnant during the course of the study or pregnancy. Women of childbearing potential, including women who had their last menstruation in the last 2 years, must have a negative urinary or serum pregnancy test. 7. Women who are breast feeding and who do not agree to discontinue nursing prior to the first study treatment and for the period defined in the protocol. 8. Sexually active men and women of childbearing potential who are not willing to use an effective contraceptive method during the study.

Contacts

Les coordonnées de l'équipe de l'essai s'affichent sur demande.

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Statut
Recrutement en cours
Phase
Phase 2
Type d'étude
Interventionnelle
Pays
Suisse
Promoteur
University of Zurich(Autre)
N° de protocole
EViDENCE-BT
Pathologies
Brain (Nervous System) Cancers, Glioblastoma, Glioma, Ependymoma, Medulloblastoma, Meningioma, Rare Primary Brain Tumors, Rare CNS Primary Tumors
Interventions
Dispositif

Traitements évalués

  • Pharmacoscopy 1.0

Collaborateurs

University Hospital, Zürich, University Hospital, Basel, Switzerland, Cantonal Hospital of St. Gallen

Lieux · 1

  • Zurich, SuisseUniversity Hospital ZurichRecrute dans ce centre

Au total, dans le monde, 1 des 3 centres listés au registre recrute ; les 2 autres ne recrutent pas actuellement.

Statut par centre selon le registre ClinicalTrials.gov (dernière mise à jour publiée : 21 septembre 2026).

Ce statut peut avoir changé et ne dit rien de votre éligibilité : avant toute démarche, vérifiez avec votre oncologue ou le centre.

Voir aussi

Autres versions

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