The purpose of the study is to assess the safety, tolerability and pharmacokinetics of AZD8055 and determine the maximum tolerated dose to take into phase II trials.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
64
Oral solution or tablet, single dose on Day 1 Part A, twice daily ascending dosing from day 8 onwards (until maximum tolerated dose is reached), cycles of 28 days treatment.
Research Site
New York, New York, United States
Research Site
Houston, Texas, United States
Research Site
Clichy, France
Research Site
Sutton, Surrey, United Kingdom
Safety and tolerability of AZD8055
Time frame: Assessed at all visits
To identify early signals of anti-tumour activity
Time frame: Visits 1, 5, and 9 and 11
To identify early signals of anti-tumor activity
Time frame: Visits 1, 5, 9 and 13
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