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Compassionate Use of Sodium Stibogluconate (Pentostam) for Cutaneous and Mucocutaneous New World Leishmaniasis
Expanded access is currently available for this treatment.
Verified by University of California, San Francisco, July 2007
Sponsored by: University of California, San Francisco
Information provided by: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT00508963
  Purpose

Patients with biopsy proven new world cutaneous or mucocutaneous leishmaniasis will be treated with sodium stibogluconate (Pentostam).


Condition Intervention
Leishmaniasis, Cutaneous
Leishmaniasis, Mucocutaneous
Drug: sodium stibogluconate (Pentostam)

MedlinePlus related topics: Leishmaniasis
Drug Information available for: Sodium stibogluconate
U.S. FDA Resources
Study Type: Expanded Access
Official Title: Compassionate Use of Sodium Stibogluconate (Pentostam) for Cutaneous and Mucocutaneous New World Leishmaniasis

Further study details as provided by University of California, San Francisco:

Intervention Details:
    Drug: sodium stibogluconate (Pentostam)
    20 mg/kg IV every day for 20 or 28 days
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Biopsy proven new world cutaneous or mucocutaneous leishmania

Exclusion Criteria:

  • Prolonged QT
  • Liver disease
  • Pancreatitis
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00508963

Contacts
Contact: Jane E Koehler, MA, MD 415-476-3536 jkoehler@medicine.ucsf.edu

Locations
United States, California
University of CA at San Francisco Hospitals and Clinics
San Francisco, California, United States, 94143
Sponsors and Collaborators
University of California, San Francisco
Investigators
Principal Investigator: Timothy Berger, MD University of CA at San Francisco
Principal Investigator: Lindy Fox, MD University of CA at San Francisco
  More Information

Study ID Numbers: UCSF Infectious Diseases
Study First Received: July 27, 2007
Last Updated: April 15, 2008
ClinicalTrials.gov Identifier: NCT00508963  
Health Authority: United States: Food and Drug Administration

Keywords provided by University of California, San Francisco:
New World Cutaneous or Mucocutaneous Leishmaniasis

Study placed in the following topic categories:
Leishmaniasis, Mucocutaneous
Leishmaniasis
Protozoan Infections
Skin Diseases, Infectious
Antimony Sodium Gluconate
Skin Diseases
Parasitic Diseases
Leishmaniasis, Cutaneous

Additional relevant MeSH terms:
Anti-Infective Agents
Antiprotozoal Agents
Antiparasitic Agents
Skin Diseases, Parasitic
Antiplatyhelmintic Agents
Therapeutic Uses
Anthelmintics
Sarcomastigophora Infections
Mastigophora Infections
Schistosomicides
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009