OncoMatch

OncoMatch/Clinical Trials/NCT04135807

Implantable Microdevice In Primary Brain Tumors

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

Early Phase 1RecruitingOliver JonasNCT04135807Data as of May 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.

Check if I qualify

Extracted eligibility criteria

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. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

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

Check if I qualify