Clinical Trials Directory

Trials / Completed

CompletedNCT01445600

ALTARGO(Retapamulin) PMS(Post-marketing Surveillance)

An Open Label, Multi-centre, Non-interventional Post-marketing Surveillance (PMS) to Monitor the Safety and Efficacy of ALTARGO(Retapamulin) Administered in Korean Patients According to the Prescribing Information

Status
Completed
Phase
Study type
Observational
Enrollment
3,612 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
9 Months
Healthy volunteers
Not accepted

Summary

This is an open label, multi-centre, non-interventional post-marketing surveillance.

Detailed description

This is an open label, multi-centre, non-interventional post-marketing surveillance to monitor the safety of ALTARGO(retapamulin) treated in Korean patients according to the prescribing information. ALTARGO is a trademark of the GlaxoSmithKline group of companies.

Conditions

Interventions

TypeNameDescription
DRUGALTARGO(retapamulin)Basically there is no treatment allocation. Subjects who would be administered of ALTARGO(retapamulin) at their physicians' discretion will be enrolled. Dosage regimen will be recommended according to the prescribing information. Subjects will be enrolled consecutively.

Timeline

Start date
2012-11-01
Primary completion
2015-08-01
Completion
2015-08-01
First posted
2011-10-04
Last updated
2015-09-23

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01445600. Inclusion in this directory is not an endorsement.