RecruitingNot ApplicableNCT05532397

Evaluation of ex Vivo Drug Combination Optimization Platform in Recurrent High Grade Astrocytic Glioma


Sponsor

National University Hospital, Singapore

Enrollment

10 participants

Start Date

Feb 17, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is an interventional, non-randomized, single site study. Brain tumor samples will be collected from patients for organoids generation and subject to panel drugs screening and QPOP analysis to derive the optimal drug combinations for treatment at the time of first high grade astrocytic glioma recurrence. The investigators hypothesize that patient-derived organoids (PDOs) mimic the biological characteristics of high grade astrocytic gliomas and serve as an ideal platform for the evaluation of drug sensitivities, accurately reflecting the patient's therapeutic response to the drugs.


Eligibility

Min Age: 21 YearsMax Age: 99 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called QPOP category 1 and a drug called QPOP category 2 for people with glioma, astrocytic. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 21 Years to 99 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGQPOP category 1

combination regimens with published data in the setting of gliomas

DRUGQPOP category 2

combination regimens where there is published data on intracranial activity and anti-glioma effect of the individual agents either as monotherapy or in combination with other agents, and where there is published safety data on the combination


Locations(2)

Department of Hematology-Oncology, National University Hospital

Singapore, Singapore

Ng Teng Fong General Hospital

Singapore, Singapore

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NCT05532397


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