Stomach Neoplasms Clinical Trial
Official title:
Phase II Trial of Single Agent AZD2014 in RICTOR Amplified or Over-expressed GC Patients as Second-line Therapy
Phase II trial of AZD2014 in RICTOR amplified or overexpressed GC patients as second-line chemotherapy AZD2014 50mg BD continuous schedule of a 28 day cycle
Tumour evaluation using RECIST 1.1 will be conducted at screening (within 28 days prior to
first dose) and every 8 weeks relative to the date of first dose, up to week 40, then every
16 weeks until objective disease progression (within a window of +/- 7 days of the scheduled
date).
Study treatment will be continued until objective disease progression (unless other criteria
for 3 treatment discontinuation are met). Patients may continue AZD2014 beyond progression
(according to RECIST 1.1), at the discretion of the investigator if they are clinically
benefiting from the treatment and they do not meet any other discontinuation criteria.
If a patient discontinues study treatment prior to disease progression, they should continue
to be assessed using RECIST 1.1 until disease progression and then followed up for survival.
Assessments for survival should be made every 8 weeks following objective disease
progression. The details of first and subsequent therapies for cancer, after discontinuation
of treatment, will be collected. The imaging modalities used for RECIST 1.1 assessment will
be CT or MRI scans of chest, abdomen and pelvis. RECIST 1.1 scans will be analysed by the
investigator on site.
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