Study identifier:D1600C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Open-Label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of the m-Tor Kinase Inhibitor AZD8055 using Intermittent Dosing Schedules in Patients with Advanced Solid Malignancies and Lymphomas
cancer
Phase 1
No
AZD8055
All
63
Interventional
18 Years +
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 May 2011 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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To investigate the safety and tolerability of AZD8055 intermittent dosing schedules when given orally to patients with advanced solid malignancies and lymphomas. Two intermittent dosing schedules will be explored with increasing doses until a maximum tolerated dose is determined for each schedule.
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: AZD8055 Oral tablet, single dose on Day 1, followed by a 48 hour – 7 day washout and then either twice daily alternate days dosing from multiple dose day 1 onwards or twice daily dosing for 21 days from multiple dose day 1 onwards followed by 7 days no treatment. Cycles of 28 days. |
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