drugset / Trial / NCT01422915

Sorbent Therapy of the Cutaneous Porphyrias

NCT01422915

Phase 2/3 Completed 4 enrolled Brigham and Women's Hospital
NaSingle-groupOpen-labelTreatment

Summary

The investigators demonstrated that cholestyramine is an effective binding agent in vitro for porphyrins. A few isolated case reports of treatment of individuals with a cutaneous porphyria suggest that cholestyramine and colestipol effectively remove porphyrins. Hypothesis: orally administered colestipol will effectively reduce sun sensitivity and lower erythrocyte porphyrin concentrations in subjects with erythropoietic protoporphyria (EPP).

Timeline

Start
2011-05
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Colestipol Unknown 2 g Oral