Safety Study of BLZ-100 in Adult Subjects With Glioma Undergoing Surgery

Subjects who provide voluntary written informed consent will be screened for eligibility. Subjects meeting all of the inclusion and none of the exclusion criteria will be eligible to participate.

Subjects will be required to arrive at the hospital (or phase 1 unit if applicable) for dosing at least 2 hours before the planned surgical excision. Following dosing, subjects will be monitored for safety and surgical excision will occur at least 2 hours after study product administration.

Inclusion criteria

• Male or female subjects aged 18- 75 years.
• Subjects must have glioma for which surgical resection is clinically indicated. Grade I, II, III and IV glioma patients will be included (for example glioblastoma, astrocytoma, and oligodendroglioma). Histological confirmation not required prior to surgery. Subjects with recurrent disease will be eligible only if the duration between last brain surgery and scheduled new surgery is ≥3 months. The grade of a recurrent tumor will be presumed that of the primary tumor for purposes of group allocation.
• Able to provide written informed consent.
• If of child-bearing potential, agree to the continued use of effective contraceptive from study entry (Informed consent) through 30 days after BLZ-100 administration.
• Available for all study visits and able to comply with all study requirements

Exclusion criteria

• Evidence of metastatic disease.
• Female who is lactating/breastfeeding
• Female with a positive pregnancy test or who is planning to become pregnant during the duration of the study.
• Karnofsky Performance Status of <60%.
• Any of the following laboratory abnormalities at Screening:

• Neutrophil count <1.5 x 10^9/L
• Platelets <75 x 10^9/L
• Hemoglobin <10 g/dL (may be determined following transfusion)
• Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3x upper limit of normal (ULN)
• Total bilirubin >1.5x upper limit of reference range (unless Gilbert's syndrome or extrahepatic source as denoted by increased indirect bilirubin fraction)
• International Normalized Ratio (INR) >1.5
• Creatinine >1.5x ULN
• Positive serology for human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis B virus (HBV).
• QTc prolongation >450 msec
• History of hypersensitivity or allergic reactions requiring corticosteroids, epinephrine and/or hospitalization.
• Uncontrolled asthma or asthma requiring oral corticosteroids.
• Known or suspected sensitivity to MRI contrast agents or excipients in the study drug product.
• Known or suspected sensitivity to Indocyanine green (ICG).
• Unstable angina, myocardial infarction, known or suspected transient ischemic events or stroke within 24 weeks of start of Screening.
• Uncontrolled hypertension.
• Receipt of photosensitizing drugs within 30 days of Screening.
• Any ongoing medications which might generate fluorescence or according to label, might generate a photochemical reaction. These include haematoporphyrin derivatives and purified fractions; Photofrin®; and the precursors of protoporphyrin IX (5-Aminolevulinic acid) used in Gliolan or Hexvix.
• Received an investigational drug or device within 30 days of enrollment.
• Prior treatment with BLZ-100.
• Any concurrent condition, including psychological and social situations, which, in the opinion of the investigator, would impact adversely on the subject or the interpretation of the study data.

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