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OncoMatch/Clinical Trials/NCT04222062

A Study Comparing GLIADEL to Stereotactic Radiosurgery in Metastatic Brain Disease

Is NCT04222062 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Carmustine 7.7Mg Wafer for brain tumor - metastatic.

Phase 2RecruitingUniversity of NebraskaNCT04222062Data as of May 2026

Treatment: Carmustine 7.7Mg WaferThis study is being done to see if adding GLIADEL to the site where the tumor was removed works as well as just having the tumor removed with radiation treatment done within six weeks after the surgery to keep the cancer from coming back.

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Extracted eligibility criteria

Cancer type

Glioblastoma

Disease stage

Metastatic disease required

Prior therapy

Cannot have received: surgery or radiation to area of planned resection

Prior treatment to the area of planned resection (surgery, radiation)

Cannot have received: whole brain radiation therapy

Prior whole brain radiation therapy

Lab requirements

Blood counts

Laboratory values adequate for patient to undergo surgery safely as determined by the attending neurosurgeon (transfusion permitted to reach goals); Normal coagulation studies (international normalized ratio, INR, ≤ 1.3)

Cardiac function

No New York Heart Association > Grade 2 congestive heart failure within 6 months prior to study entry, unless asymptomatic and well controlled with medication; No uncontrolled or significant cardiovascular disease, clinically significant ventricular arrhythmia (such as ventricular tachycardia, ventricular fibrillation, or Torsades des pointes)

Laboratory values adequate for patient to undergo surgery safely as determined by the attending neurosurgeon (transfusion permitted to reach goals); Normal coagulation studies (international normalized ratio, INR, ≤ 1.3); Severe pulmonary, cardiac or other systemic disease, specifically: New York Heart Association > Grade 2 congestive heart failure within 6 months prior to study entry, unless asymptomatic and well controlled with medication; Uncontrolled or significant cardiovascular disease, clinically significant ventricular arrhythmia (such as ventricular tachycardia, ventricular fibrillation, or Torsades des pointes), clinically significant pulmonary disease (such as ≥ Grade 2 dyspnea, according to Common Terminology Criteria for Adverse Events 5.0)

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

US trial sites

  • Henry Ford · Detroit, Michigan
  • University of Nebraska Medical Center · Omaha, Nebraska

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