Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
The Christie NHS Foundation Trust
With
AstraZeneca
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
histological confirmation of prostate adenocarcinoma
documented evidence of bone metastasis on bone scan or MRI
biochemical progression of prostate cancer
surgically or medically castrate with serum testosterone ≤2.4nmol/L
ECOG performance status 0 - 2
life expectancy of 6 months or more.
You may not be if
radiotherapy to bone lesion or prostatic bed within 4 weeks of starting study treatment.
prior targeted cancer therapies (such as gefitinib, bevacizumab)
systemic radionuclide therapy within 12 weeks of starting study treatment.
current therapy, within 4 weeks of study entry with potent inhibitors of CYP3A4 (ketoconazole, itraconazole, ritonavir, indinavir, erythromycin, troleandomycin, clarithromycin, diltiazem and verapamil), inhibitors of CYPs 2D6 and 2C9 (quinidine and fluconazole), and potent P450 inducers (phenytoin, rifampicin, carbamazepine and phenobarbitone)
definite or suspected personal history or family history of adverse drug reactions, or hypersensitivity to drugs that are endothelin antagonists
ineligibility for MRI scanning includes standard MRI criteria (for example, metal implants such as cochlear implants, cardiac pacemakers, heart valves, aneurysm clips and metal fragments in eyes) and patients known to be allergic to gadolinium-based MRI contrast agents
Clareo Health | Window Study of ZD4054 in Metastatic Prostate Cancer
