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Clinical Trial Summary

To investigate the severity of secondary Raynaud's disease-related attacks during the 14 days 2101 dosing period.


Clinical Trial Description

1. Number and cumulative duration of Raynaud's attacks. 2. Adverse events and changes in vital signs. 3. SLx-2101 pharmacokinetic parameters derived after dosing on Day 1 and Day maximum plasma concentration (Cmax), area under the plasma concentration-time curve (AUC0-4), time to Cmax (tmax), and accumulation ratio ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00528242
Study type Interventional
Source Response Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date June 2007
Completion date March 2008

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