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Phase I Study of Isotretinoin in Patients With Recessive Dystrophic Epidermolysis Bullosa

Epidermolysis Bullosa Clinical Trial

Clinical Trial Summary

OBJECTIVES:

I. Determine the safety of isotretinoin in patients with recessive dystrophic epidermolysis bullosa.

Clinical Trial Description

PROTOCOL OUTLINE:

Patients receive oral isotretinoin daily for 8 months in the absence of disease progression or unacceptable toxicity.

Completion date provided represents the completion date of the grant per OOPD records ;

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00014729
Study type Interventional
Source FDA Office of Orphan Products Development
Contact
Status Completed
Phase Phase 1
Start date October 2000
Completion date September 2002
View Details
See also
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