To Assess the Safety of Continuous IV Administration of Plerixafor in Patients With Advanced Pancreatic, Ovarian and Colorectal Cancers

• Status: Completed
• Trial end date: 2018-12-14
• Target enrollment: 0
• Participant gender: All

Summary

Pancreatic, ovarian and colorectal cancers are difficult to treat using chemotherapy and immune therapies.Currently most patients are offered treatment with a standard chemotherapy drug depending on their cancer type. Recently, laboratory studies have shown that a drug called plerixafor may help the body to overcome resistance to immune therapy.

The purpose of this study is to find out if the study drug has the same effect on patients with advanced pancreatic, ovarian or colorectal cancer, as we have seen in our laboratory experiments, and find out the right dose of the study drug to give. This is a 'dose escalation study'. Patients will be recruited slowly and the study team will closely monitor the effect the drug has, until they find the best dose to give. As part of this study, blood and tumour samples will be collected and analysed in our laboratories and the patients cancer will be monitored using two imaging techniques, CT and FDG-PET scans.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: CCTU- Cancer Theme
• Collaborators: CRUK Cambridge Institute; Lustgarten Foundation; National Institute for Health Research, United Kingdom; Sanofi; Stand Up To Cancer
• Treatments: JM 3100; Plerixafor

Criteria

Inclusion Criteria:

• Aged 16 years or over at the time of signing informed consent form.

• Dose escalation phase only: Patients with inoperable, histologically proven locally advanced or metastatic pancreatic, high grade serous ovarian or colorectal adenocarcinoma, refractory to conventional chemotherapy or a patient who has declined conventional chemotherapy. OR;

• Expansion phase only: Patients with inoperable, histologically proven locally advanced or metastatic pancreatic, refractory to conventional chemotherapy or a patient who has declined conventional chemotherapy.

• Tumour lesions considered to be accessible for core biopsy and immunostaining assessment.

• ECOG performance status 0-1.

• Life expectancy of at least 12 weeks.

• All women of child-bearing potential and all sexually active male patients must agree to use effective contraception methods throughout the study and for 3 months after the final dose of study drug.

Exclusion Criteria:

• Inadequate haematological function defined by:

• Absolute neutrophil count (ANC) <1.5 x 109/L

• Absolute lymphocyte count < normal level for institution

• Haemoglobin <9.0 g/dL (90 g/L) (may be increased to this level with transfusion as long as there is no evidence of active bleeding)

• Platelets <100 x 109/L

• Clotting; INR >1.3

• Inadequate renal function defined by calculated creatinine clearance by Cockcroft-Gault of <50 ml/min.

• Inadequate hepatic function defined by:

• Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) >2.5 x upper limit of normal (ULN) or >5 x in the presence of liver metastases

• Total bilirubin >1.5 x ULN

• Current treatment (within 28 days of entry) with chemotherapy, steroids or other immunosuppressive drugs.

• Significant acute or chronic medical or psychiatric condition, disease or laboratory abnormality which in the judgment of the Investigator would place the patient at undue risk or interfere with the study.

• Cardiac co-morbidity:

• Past history of significant rhythm disturbance (e.g. SVT, AF or ventricular irregularities)

• Requirement for pacemaker.

• Myocardial infarction in the previous 6 months.

• Known medical history of proven postural hypotension.

• Active infection.

• Patients with known allergy to plerixafor or its excipients.

• Patients known to have hepatitis B, hepatitis C or HIV infection.

• Women, who are pregnant, plan to become pregnant or are lactating (during the study or for up to 3 months after the last dose)