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OncoMatch/Clinical Trials/NCT04135807

Implantable Microdevice In Primary Brain Tumors

Is NCT04135807 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies Microdevice for grade ii glioma.

Early Phase 1RecruitingOliver JonasNCT04135807Data as of Jun 2026

Treatment: MicrodeviceThis pilot study will assess the safety and feasibility of using an implantable microdevice to measure local intratumor response to chemotherapy and other clinically relevant drugs in malignant brain tumors. * The device involved in this study is called a microdevice. * The drugs used in this study will only include drugs already used systemically for the treatment of gliomas.

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Extracted eligibility criteria

Treatments studied

Other

Microdevice

Cancer type

Glioblastoma

Disease stage

Required: Stage II, III, IV (WHO grade)

Grade: IIIIIIV (WHO)

WHO grade II-IV glioma

Prior therapy

Cannot have received: chemotherapy

Participants who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas) prior to entering the study

Cannot have received: radiotherapy

Participants who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas) prior to entering the study

Cannot have received: investigational agent

Participants who are receiving any other investigational agents

Lab requirements

Blood counts

Leukocytes ≥ 3,000/mcL; Absolute neutrophil count ≥ 1,500/mcL; Platelets ≥ 100,000/mcL

Kidney function

Creatinine within normal institutional limits OR Creatinine clearance ≥ 60 mL/min/1.73 m2 for participants with creatinine levels above institutional normal

Liver function

Total bilirubin within normal institutional limits; AST(SGOT)/ALT(SGPT) ≤ 2.5 × institutional upper limit of normal

Participants must have normal organ and marrow function as defined below: * Leukocytes ≥ 3,000/mcL * Absolute neutrophil count ≥ 1,500/mcL * Platelets ≥ 100,000/mcL * Total bilirubin within normal institutional limits * AST(SGOT)/ALT(SGPT) ≤ 2.5 × institutional upper limit of normal * Creatinine within normal institutional limits OR * Creatinine clearance ≥ 60 mL/min/1.73 m2 for participants with creatinine levels above institutional normal.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Brigham and Women's Hospital · Boston, Massachusetts

Showing up to 5 US sites.

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Frequently asked questions

Is NCT04135807 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, radiotherapy, investigational agent disqualifies patients from enrollment.

What disease stage is eligible?

Stage II or III or IV is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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Related pages

Glioblastoma trials