Study identifier:D0102C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1, Open-label, Multiple-dose, Dose escalation Study to Assess the Safety, Tolerability and Pharmacokinetics of AZD8931 in Patients with Advanced Solid Malignancies
Advanced solid malignancies
Phase 1
No
AZD8931
All
28
Interventional
18 Years - 150 Years
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Jan 2014 by AstraZeneca
AstraZeneca
-
The main purpose of this study is to explore the safety and tolerability of multiple ascending doses (MAD) of AZD8931 in patients with advanced solid malignancies
Location
Location
Moscow, Russian Federation
Location
St. Petersburg, Russian Federation
Location
Berlin, Germany
Location
Berlin, Germany
Location
Moscow, Russian Federation
Location
Saint Petersburg, Russian Federation
Location
St. Petersburg, Russian Federation
Location
St-Petersburg, Russian Federation
Arms | Assigned Interventions |
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