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Clinical Trial Summary

Study of tolerability and efficacy of BVS857 in severe burn subjects over 8 weeks and 15 weeks


Clinical Trial Description

No formal analysis was performed as study was terminated due to low enrollment issues. (n=1 patient was enrolled) ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Burns
  • Hypercatabolic Status Related to Severe Burn

NCT number NCT02074995
Study type Interventional
Source Novartis
Contact
Status Terminated
Phase Phase 2
Start date February 2014
Completion date January 2015