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Clinical Trials/NCT00233545
NCT00233545
Completed
Phase 2

Miltefosine to Treat Cutaneous Leishmaniasis in Bolivia

AB Foundation1 site in 1 country80 target enrollmentSeptember 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Cutaneous Leishmaniasis
Sponsor
AB Foundation
Enrollment
80
Locations
1
Primary Endpoint
cure rate
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Cutaneous leishmaniasis is typically treated with the parenteral product pentavalent antimony. Miltefosine is an oral agent shown to be active for mucosal leishmaniasis due to L braziliensis in Bolivia and cutaneous leishmaniasis due to L panamensis in Colombia. This trial is intended to evaluate miltefosine for cutaneous leishmaniasis due to L braziliensis in Bolivia. Patients will be randomly assigned to miltefosine or pentavalent antimony. Standard dose regimens will be used for both drugs.

Registry
clinicaltrials.gov
Start Date
September 2005
End Date
September 2007
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
AB Foundation

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

cure rate

Study Sites (1)

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