Status:
COMPLETED
A Phase 1 Study of Dexanabinol in Patients With Advanced Solid Tumours
Lead Sponsor:
e-Therapeutics PLC
Conditions:
Solid Tumour
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This study is a trial of Dexanabinol in patients with advanced solid tumours. The purposes of this protocol are to study different doses of the study drug to determine the maximum safe dose and to fur...
Eligibility Criteria
Inclusion
- 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informed consent prior to any study-specific Screening procedures, with the understanding that the consent may be withdrawn by the patient at any time without prejudice.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
- 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.
Key Trial Info
Start Date :
January 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2015
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT01489826
Start Date
January 1 2012
End Date
July 1 2015
Last Update
February 9 2017
Active Locations (3)
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1
Leeds Cancer Centre at St. James's University Hospital
Leeds, England, United Kingdom, LS9 7TF
2
Northern Centre for Cancer Care, Freeman Hospital, Newcastle-upon-Tyne, UK
Newcastle upon Tyne, Tyne and Wear, United Kingdom, NE7 7DN
3
The Beatson West of Scotland Cancer Centre,
Glasgow, United Kingdom, G12 0YN