AZD6765 Oral Single Ascending Dose/Multiple Ascending Dose (SAD/MAD)
Summary
The purpose of this study is to determine the safety of AZD6765 when given in single and multiple oral doses and to compare an oral and intravenous (IV) formulation of AZD6765 to placebo.
Study Design
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)
Conditions
Intervention
AZD6765, AZD6765
Location
Research Site
Overland Park
Kansas
United States
Status
Suspended
Source
Results (where available)
Links
- Source: http://clinicaltrials.gov/show/NCT00963365
- Information obtained from ClinicalTrials.gov on July 15, 2010
Published on BioPortfolio: 2014-08-27T03:19:51-0400
Clinical Trials
This study will provide data to support preclinical to clinical translation by aligning preclinical and clinical efficacy assay with dose dependent changes in EEG.
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