drugset / Trial / NCT01056341

Study to Demonstrate the Efficacy and Safety of Propranolol Oral Solution in Infants With Proliferating Infantile Hemangiomas Requiring Systemic Therapy

NCT01056341

Phase 2/3 Completed 512 enrolled Pierre Fabre Dermatology
RandomizedParallel-groupQuadruple-blindTreatment

Summary

There is an unsatisfied medical need for a first-line treatment of proliferating IHs with a good benefit/risk profile. Based on the recent findings of encouraging results obtained with propranolol in a series of infants with severe Infantile Hemangioma (IH), propranolol is expected to be of significant benefit in the management of the condition. The present study has been designed to confirm efficacy of propranolol in severe IH by demonstrating superiority over placebo and to document the safety profile of propranolol in this indication.

Timeline

Start
2010-01
Primary completion
2012-05
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Propranolol Small molecule 1 mg/kg Oral
Subject Propranolol Small molecule 3 mg/kg Oral

Indications