Stocrin Re-examination Study (0831-028)
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|ClinicalTrials.gov Identifier: NCT01065792|
Recruitment Status : Completed
First Posted : February 9, 2010
Last Update Posted : July 21, 2015
This survey is conducted for preparing application materials for re-examination under the Pharmaceutical Affairs Laws and its Enforcement Regulation, its aim is to reconfirm the clinical usefulness of STOCRIN through collecting the safety and efficacy information according to the Re-examination Regulation for New Drugs.
Post-marketing surveys are not considered applicable clinical trials and thus the results of this survey will not be posted at its conclusion. The results will be submitted to public health officials as required by applicable national and international laws.
|Condition or disease|
|Study Type :||Observational|
|Actual Enrollment :||728 participants|
|Official Title:||Re-examination Study for General Drug Use to Assess the Safety and Efficacy Profile of STOCRIN in Usual Practice|
|Study Start Date :||March 2009|
|Actual Primary Completion Date :||February 2014|
|Actual Study Completion Date :||February 2014|
Patients with HIV-1 infection taking Stocrin
- Percent of patients with any adverse experience [ Time Frame: Up to 14 days following cessation of treatment ]
- Proportion of patients with HIV-1 RNA levels of less than 400 copies per milliliter after treatment [ Time Frame: At 12 weeks +/- 2 weeks and at 24 weeks +/- 2 weeks after first treatment ]
- Change from baseline in CD4 cell count and overall efficacy evaluation by investigator (success, failure or can not be assessed) [ Time Frame: At 12 weeks +/- 2 weeks and at 24 weeks +/- 2 weeks after first treatment ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01065792
|Study Director:||Medical Monitor||Merck Sharp & Dohme Corp.|