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Clinical Trial Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the LPD (unknown adverse drug reaction), 2) the incidence of adverse drug reactions in this surveillance, and 3)factors considered to affect the safety and/or efficacy of this drug.


Clinical Trial Description

All the patients whom an investigator prescribes the first CELSENTRI® Tablets should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into the investigation at random. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00864474
Study type Observational
Source ViiV Healthcare
Contact
Status Completed
Phase
Start date March 31, 2010
Completion date December 24, 2018