Solid Tumors Clinical Trial
Official title:
An Open-label, Non-randomised, Multicentre Study to Allow Continued Access to and Assess the Safety and Tolerability of AZD1775 for Patients Enrolled in AZD1775 Clinical Pharmacology Studies
Open-label, non-randomised study to provide continued access to AZD1775 for patients with advanced solid tumours who have previously completed an AZD1775 clinical pharmacology study and to investigate the safety of AZD1775.
This is an open-label, non-randomised study designed to provide continued access to AZD1775
for eligible patients with advanced solid tumours who have previously completed an AZD1775
clinical pharmacology study and to investigate the safety of a once daily monotherapy regimen
of AZD1775 in patients with advanced solid tumours.
All patients who completed 1 of the parent clinical pharmacology studies are eligible for
this study after a washout period of at least 4 days (minimum duration defined in the parent
study protocol) and meet the eligibility criteria specified in this protocol. Patients who
discontinue early from the parent study will be considered by the Sponsor and treating
physician on a case-by-case basis.
During the study, patients will continue to receive AZD1775 as long as they are benefiting
from treatment in the Investigator's opinion and do not meet any other discontinuation
criteria.
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---|---|---|---|
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