A Phase 1 Study of Dexanabinol in Patients With Advanced Solid Tumours

Inclusion criteria

• Adult patients defined by age ≥18 years.
• Patients with histologically or cytologically confirmed solid tumours that are advanced, metastatic and or progressive, for whom there is no effective standard therapy available.
• Eastern Collaborative Oncology Group (ECOG) Performance Status of ≤2.
• Any acute or chronic adverse effects of prior chemotherapy or radiotherapy have resolved to < Grade 2 as determined by Common Terminology Criteria for Adverse Events (CTCAE) v4.03 criteria, with the exception of alopecia.
• Evaluable disease, either measurable on imaging, or with informative tumour marker(s), as assessed by Response Evaluation Criteria In Solid Tumors (RECIST) v1.1 (Eisenhauer, et al. 2009).
• Laboratory values at Screening:

• Absolute neutrophil count ≥1.5 x 109/L;
• Platelets ≥100 x 109/L;
• Total bilirubin <1.5 times the upper limit of normal;
• Aspartate aminotransferase (AST) ≤2.5 times the upper limit of normal;
• Alanine aminotransferase (ALT) ≤2.5 times the upper limit of normal;
• Estimated glomerular filtration rate (GFR) of >50 mL/min (based on the Wright formula (Wright, et al. 2001); and
• Negative human chorionic gonadotropin (hCG) test in women of childbearing potential (defined as women ≤50 years of age or history of amenorrhea for ≤12 months prior to study entry). Sexually active male and female patients of childbearing potential must agree to use an effective method of birth control (e.g. barrier methods with spermicides, oral or parenteral contraceptives and/or intrauterine devices) during the entire duration of the study and for 1 month after final administration of Dexanabinol, or the patient must be surgically sterile (with documentation in the patient's medical records).
• If there is a history of treated brain metastases, these must have been clinically stable for ≥4 weeks prior to enrollment.
• Have a life expectancy of >3 months.
• Ability to give written, informed consent prior to any study-specific Screening procedures, with the understanding that the consent may be withdrawn by the patient at any time without prejudice.
• Be willing and able to comply with the study protocol procedures.

Exclusion criteria

• Patient is pregnant or breast feeding.
• History of clinically significant cardiac condition, including ischemic cardiac event, myocardial infarction or unstable cardiac disease within 3 months of Cycle 1, Day 1.
• Chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to Cycle 1, Day 1. Localised palliative radiotherapy is permitted for symptom control.
• Major surgery within 6 weeks prior to Cycle 1, Day 1.
• Known human immunodeficiency virus positivity.
• Active hepatitis B or C or other active liver disease (other than malignancy).
• Use of any investigational agents within 4 weeks of Cycle 1, Day 1.
• Any active, clinically significant, viral, bacterial, or systemic fungal infection within 4 weeks prior to Cycle 1, Day 1.
• History of significant chronic or recurrent infections requiring treatment or any uncontrolled intercurrent illness that would jeopardize patient safety, interfere with the objectives of the protocol, or limit patient compliance with study requirements, as determined by the Investigator.