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
| Type | Name | Description |
|---|---|---|
| DRUG | ALTARGO(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.