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OncoMatch/Clinical Trials/NCT06160206

Retifanlimab with Bevacizumab and Hypofractionated Radiotherapy for the Treatment of Recurrent Glioblastoma

Is NCT06160206 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Bevacizumab and Retifanlimab for recurrent glioblastoma.

Phase 2RecruitingAcademic and Community Cancer Research UnitedNCT06160206Data as of May 2026

Treatment: Bevacizumab · RetifanlimabThis phase II trial tests how well retifanlimab with bevacizumab and hypofractionated radiotherapy, compared to bevacizumab and hypofractionated radiotherapy alone, works in treating patients with glioblastoma that has come back after a period of improvement (recurrent). A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as retifanlimab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the formation of blood vessels that bring oxygen and nutrients to tumor. This may slow the growth and spread of tumor. Hypofractionated radiation therapy delivers higher doses of radiation therapy over a shorter period of time and may kill more tumor cells and have fewer side effects. Giving retifanlimab with bevacizumab and hypofractionated radiotherapy may work better in treating patients with recurrent glioblastoma than bevacizumab and hypofractionated radiotherapy alone.

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Extracted eligibility criteria

Cancer type

Glioblastoma

Disease stage

Required: Stage IV (WHO)

Grade: 4 (WHO)

Recurrent World Health Organization (WHO) grade IV glioblastoma

Prior therapy

Cannot have received: investigational agent

Exception: not considered treatment for the primary neoplasm ≤ 2 weeks prior to registration

Receiving any other investigational agent which would be considered treatment for the primary neoplasm ≤ 2 weeks prior to registration

Lab requirements

Blood counts

anc ≥ 1,500/mm^3; platelet count ≥ 100,000/mm^3; hemoglobin ≥ 9.0 g/dl

Kidney function

creatinine ≤ 1.5 x uln

Liver function

total bilirubin ≤ 1.5 x uln; alt and ast ≤ 3 x uln (≤ 5 x uln for patients with liver involvement)

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

US trial sites

  • Mayo Clinic in Arizona · Scottsdale, Arizona
  • Mayo Clinic in Florida · Jacksonville, Florida
  • Mayo Clinic · Rochester, Minnesota

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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