Inclusion Criteria:

          1. Histologically confirmed glioblastoma multiforme (GBM) and are at first or second
             relapse.

          2. ≥ 18 years of age

          3. Have measurable disease of at least one solitary lesion with a dimension between 1 cm
             and 5 cm according to RANO

          4. Karnofsky performance status (KPS) ≥ 60

          5. Adequate organ function defined by laboratory values as follows: Creatinine < 140
             µmol/L (1.6 mg/dL); if borderline, the creatinine clearance ≥40 mL/min, Bilirubin <
             20% above the upper limit of normal, AST and ALT ≤ 2.5 the upper limit of normal.

          6. Absolute Neutrophil count baseline (ANC) ≥1500 cells/uL, Hemoglobin baseline ≥ 9.0
             g/dL and Platelets baseline ≥ 100,000 cells/uL prior to the start of study treatment.

          7. Female of childbearing potential (FCBP) must not be pregnant and agree to not becoming
             pregnant for at least 42 days following the start of the treatment.

          8. Patients with HIV/AIDs are eligible if they have not had an opportunistic infection
             within the past 12 months

          9. Patients with chronic HBV infection or patients with current or a history of HCV
             infection are allowed if:

               1. have an HBV viral load below the limit of quantification and be on viral
                  suppressive therapy

               2. have current HCV infection, they should be on concurrent HCV treatment and the
                  HCV viral load must be below the limit of quantification

               3. have a history of HCV infection should have completed curative antiviral
                  treatment and require HCV viral load below the limit of quantification

        Exclusion Criteria:

          1. Had prior radiation therapy within 12 weeks of screening MRI unless there is
             unequivocal histological confirmation of tumor progression

          2. Subjects on growth factors therapy with less than 4 weeks washout period (for
             short-acting growth factors, such as G-CSF, GM-CSF 5-day wash-out for longer-acting
             factors (such as Neulasta) 10 days

          3. Radiotherapy, chemotherapy, or other investigational agents within 4 weeks

          4. Prior cellular or gene therapy at any time

          5. Clinical or laboratory signs for immunodeficiency or under immunosuppressive
             medication or steroids greater than15 mg prednisone or equivalent per day

          6. History of malignancy, other than GBM, unless the subject has been free of disease for
             > 3 years from the date of signing the ICF. Exceptions include the following
             noninvasive malignancies: basal cell carcinoma of the skin, squamous cell carcinoma of
             the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, Incidental
             histological finding of prostate cancer (TNM stage of T1a or T1b)

          7. Active autoimmune disease other than controlled connective tissue disorder or those
             who are not on active therapy