Rollover Study Protocol for Pediatric Patients in South Africa for Continued Access to Emtricitabine

Phase 2

Completed

Brief Summary: The primary objectives of this trial are to provide FTC-203 study participants in South Africa with continued access to the study drug, emtricitabine (FTC), following completion of the FTC-203 study and to collect long-term safety information in participants receiving emtricitabine in combination with other antiretroviral agents.

Recruitment & Eligibility

Inclusion Criteria

Complete or have previously completed at least through the Week 96 Visit (i.e., 96 weeks on study) for the FTC-203 study.
Complete all End-of-Study Visit procedures for the FTC-203 study.
Either (a) have a plasma HIV-1 RNA viral load of ≤ 400 copies/mL at the End-of-Study Visit for the FTC-203 study, or (b) if the subject's plasma HIV-1 RNA viral load at the End-of-Study Visit for FTC-203 study is > 400 copies/mL, their viral load is < 1.0 log10 above the nadir recorded after Week 8 of the FTC-203 study and there is reliable genotypic evidence showing a lack of resistance to emtricitabine.
A parent or other legal guardian has provided written informed consent to the subject participating in the rollover protocol. As applicable, based on the subject's age and normal institution practice, the subject should additionally provide their written informed consent or assent to participate in the rollover protocol.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Exclusion Criteria

Not provided

Arm && Interventions

Group	Intervention	Description
Emtricitabine	Emtricitabine	Participants will receive emtricitabine for as long as they continue to meet specific virologic criteria and until either: (1) the participant chooses to discontinue treatment of emtricitabine and withdraw from the rollover protocol; (2) the participant experiences a toxicity that necessitates the permanent discontinuation of emtricitabine, or (3) emtricitabine is approved for market distribution in the participant's country of residence.

Primary Outcome Measures

Name	Time	Method
Number of Participants Who Had Access to, and Received the Intervention	Up to 586 weeks	This endpoint has been included to satisfy the requirements of ClinicalTrials.gov. However, there were no prespecified endpoints in this study.

Secondary Outcome Measures

Name	Time	Method

Locations (2): Perinatal HIV Research Unit, Chris Hani Baragwanath Hospital
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Soweto, South Africa
Themba Lethu Clinic, Helen Joseph Hospital, Westdene
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Johannesburg, South Africa