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Clinical Trial Summary

The study is an investigation to assess the capacity of ascending doses of CX1739 to antagonize the respiratory depressive effect of remifentanil. The study will also investigate whether ascending doses of CX1739 reduce the analgesic effect of remifentanil or alter the BIS measure of sedation and will evaluate the safety of CX1739 when used in conjunction with remifentanil.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02735629
Study type Interventional
Source RespireRx
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 2016
Completion date September 2016