PAZOFOS: Phase Ib and Phase II Trial of Pazopanib +/- Fosbretabulin in Advanced Recurrent Ovarian Cancer

Exclusion Criteria

• •Radiotherapy, surgery or tumour embolisation within 28 days before the first dose of IMP
• •Endocrine therapy, immunotherapy or chemotherapy during the previous four weeks (six weeks for nitrosoureas, Mitomycin-C and six weeks for investigational medicinal products) before the first dose of IMP.
• •Ongoing grade ≥ 2 toxic manifestations of previous treatments. Exceptions to this are alopecia or certain Grade 1 toxicities, which in the opinion of the Chief and Principal Investigators should not exclude the patient; and grade 1 or 2 neurotoxicity considered to be due to paclitaxel.
• •Female patients who are able to become pregnant (or are already pregnant or lactating). Those who have a negative serum or urine pregnancy test before enrolment and agree to use two highly effective forms of contraception (oral, injected or implanted hormonal contraception and condom, have an intra-uterine device and condom, diaphragm with spermicidal gel and condom) for four weeks before entering the trial, during the trial and for six months afterwards are considered eligible.
• •Major thoracic or abdominal surgery from which the patient has not yet recovered.
• •At high medical risk because of non-malignant systemic disease including active uncontrolled infection.
• •Known to be serologically positive for hepatitis B, hepatitis C or human immunodeficiency virus (HIV).
• •History of any of the following cardiovascular conditions within the last six months:
• •* Coronary revascularisation (percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG))
• •* Acute coronary syndrome (myocardial infarction (MI), unstable angina)
• •* Symptomatic peripheral vascular disease
• •* Class III or IV congestive heart failure, as defined by the New York Heart Association (NYHA) (Appendix 4)
• •Patients who have sustained hypertension, defined as a systolic blood pressure (SBP) of \> 140 mm Hg or diastolic blood pressure (DBP) of \> 90 mm Hg, on three occasions.
• •ECG with evidence of clinically significant abnormalities.
• •Patients with a QTc\> 480ms or taking any drug known to prolong the QTc interval that cannot be stopped for the duration of the trial (Appendix 4).
• •Patients with pathologic bradycardia (\<60 b/m in non-athletes), heart block (excluding first-degree block, being PR interval prolongation only).
• •History of cerebrovascular accident (including transient ischaemic attack (TIA)), pulmonary embolism or untreated deep vein thrombosis (DVT) within the past six months. Patients with recent DVT or pulmonary embolism who have been treated with therapeutic anti-coagulant agents for at least six weeks will be eligible, provided their INR (if taking oral anti-coagulants) has been stable for this period of time.
• •History or clinical evidence of central nervous system (CNS) metastases or leptomeningeal carcinomatosis, except for individuals who have previously treated CNS metastases, are asymptomatic and have had no requirement for steroids or anti-convulsant medication for six months prior to the first dose of IMP.
• •Clinically significant abnormalities that may increase the risk of gastrointestinal bleeding or perforation, including but not limited to:
• •* Bleeding: Active peptic ulcer disease, known intraluminal metastatic lesions with risk of bleeding, Inflammatory bowel disease (Crohn's disease, ulcerative colitis);
• •* Perforation: History of abdominal fistula or large pelvic mass; gastrointestinal perforation or intra-abdominal abscess within four weeks prior to first dose of IMP; previous bowel surgery which is judged by the investigator to increase significantly the risk of gastrointestinal complications from trial treatment
• •Evidence of active bleeding or bleeding diathesis.
• •Transfusion within one week prior to first dose of IMP.
• •Known endobronchial lesions and/or lesions infiltrating major pulmonary vessels.
• •Clinically significant haemoptysis, within eight weeks before the first dose of IMP.
• •Previous treatment with pazopanib.
• •Any participant that is participating in (or plans to participate in) another interventional clinical trial, whilst taking part in this Phase Ib/II study of fosbretabulin and pazopanib. Participation in an observational trial would be acceptable.
• •Any other condition which in the Investigator's opinion would not make the patient a good candidate for the clinical trial.
• •Current malignancies of other types, with the exception of adequately treated cone-biopsied in situ carcinoma of the cervix uteri and basal or squamous cell carcinoma of the skin and no evidence of recurrence of other malignancy for at least 2 years.
• •Hypersensitivity to Pazopanib or any of it's excipients