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Clinical Trial Summary

In the SHIELD study, the study sponsor seeks to assess safety, PK and antiviral activity for children and adolescents with dual or triple class resistance. It will also assess the acceptability and swallowability of formulation among the pediatric population. The dose selection of FTR for children and adolescents ≥20kg utilized a population pharmacokinetic (POP PK) model-based approach to achieve similar adult TMR exposures following FTR 600mg BID administration with combination therapy that was demonstrated to be safe and effective in the FTR Phase 3 BRIGHTE study in HTE patients.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04648280
Study type Interventional
Source PENTA Foundation
Contact Pablo Rojo
Phone 7169822
Email pablorojoconejo@netscape.net
Status Recruiting
Phase Phase 1/Phase 2
Start date June 30, 2022
Completion date June 2028