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No longer availableNCT00508963Updated Dec 27, 2023

Compassionate Use of Sodium Stibogluconate (Pentostam) for Cutaneous and Mucocutaneous New World Leishmaniasis

An expanded access record providing sodium stibogluconate (Pentostam) in Leishmaniasis, Cutaneous and Leishmaniasis, Mucocutaneous, sponsored by University of California, San Francisco. No longer available at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-12-27.

Sponsored by University of California, San Francisco · Expanded access

Study type
Expanded access
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

  • Leishmaniasis, Cutaneous
  • Leishmaniasis, Mucocutaneous

Keywords

  • New World Cutaneous or Mucocutaneous Leishmaniasis
03

In context

Leishmaniasis

185 studies on the registry are indexed under Leishmaniasis; 15 are open to participants now.

Browse Leishmaniasis studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,132 studies on the registry; 375 are open to participants now.

Of its 262 completed or terminated interventional studies of FDA-regulated products, 196 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All

Inclusion criteria

  • Biopsy proven new world cutaneous or mucocutaneous leishmania

Exclusion criteria

Exclusion Criteria:

  • Prolonged QT
  • Liver disease
  • Pancreatitis
05

Access details

Study type
Expanded access

Available treatment

  • Drugsodium stibogluconate (Pentostam)

    20 mg/kg IV every day for 20 or 28 days

06

Where to request access

1 site
  • University of CA at San Francisco Hospitals and Clinics
    San Francisco, California 94143, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 27, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00508963
Lead sponsor
University of California, San Francisco
Responsible party
Sponsor
First posted
Jul 30, 2007
Last update
Dec 27, 2023

Study contacts

Brian Schwartz, MD
principal investigator · University of CA at San Francisco
Kanade Shinkai, MD
principal investigator · University of CA at San Francisco
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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Discussion

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