drugset / Trial / NCT00454818

Efficacy and Safety Study of Genetically Targeted Enzyme Replacement Therapy for Advanced Heart Failure

NCT00454818 ↗

Phase 1/2 Completed 51 enrolled Celladon Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is divided into 2 parts. In the first part, the safety of the gene transfer agent MYDICAR® will be evaluated. In the second part, the ability of MYDICAR® to improve heart function will be studied.

Timeline

Start
2007-03
Primary completion
2010-08
Completion
2012-08

Outcome

Met primary endpoint

paper met the prespecified criteria for success at the group-level, individual-level, and outcome analyses (cardiovascular hospitalizations) at 6 months PMID 21709064 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject MYDICAR Gene therapy (AAV / viral vector) 1.4e+11 unknown Other
Subject MYDICAR Gene therapy (AAV / viral vector) 6e+11 unknown Other
Subject MYDICAR Gene therapy (AAV / viral vector) 3e+12 unknown Other
Subject MYDICAR Gene therapy (AAV / viral vector) 1e+13 unknown Other