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TerminatedNCT00001128Updated Dec 14, 2016

Treatment of Chronic Cryptosporidiosis in AIDS Patients

An interventional study of Interleukin-12 and Paromomycin sulfate in Cryptosporidiosis and HIV Infections, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Terminated at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-12-14.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
16
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to see if it is safe and effective to add interleukin-12 (IL-12) to the standard drug combination (paromomycin plus azithromycin) used to treat cryptosporidiosis in AIDS patients. Doctors would like to find out if the combination of IL-12, paromomycin, and azithromycin is more effective than paromomycin and azithromycin alone.

Cryptosporidiosis is a type of opportunistic (AIDS-related) infection seen in HIV-positive patients as their immune systems weaken. It is caused by a parasite that invades the intestinal tract, and it can cause watery diarrhea, stomach cramps, an upset stomach, or a fever. Antibiotics (paromomycin and azithromycin) are usually used to treat cryptosporidiosis. In this study, doctors will look at the effectiveness of using IL-12. IL-12 is a type of protein naturally produced by certain types of cells of the immune system and is believed to be important for immune function. Doctors hope that IL-12 can help boost the immune system in fighting cryptosporidiosis.

Read the detailed description

Cryptosporidium parvum, an intracellular protozoan parasite, is a frequent cause of chronic diarrhea in HIV-infected patients, causing significant morbidity and mortality. Highly effective antiparasitic treatment for this infection is not currently available. Paromomycin and azithromycin have some efficacy and have been used in combination in a small number of patients. Immune reconstitution with highly active antiretroviral therapy appears to be the most effective therapy, but this is not possible for all patients. Interferon gamma expression is strongly associated with control of cryptosporidiosis, and IL-12 is the cytokine primarily responsible for stimulation of interferon gamma expression in vivo. It is hoped that treatment with recombinant human IL-12 can result in stimulation of an intestinal cytokine response in AIDS patients with cryptosporidiosis and that response combined with chemotherapy can lead to the elimination of detectable numbers of Cryptosporidium oocysts from the stools.

All patients receive azithromycin and paromomycin, and patients are randomized to add either IL-12 or placebo. IL-12 (or placebo) injections are given twice a week. Patients take their study medications for 4 weeks. During this time, they will be asked to record bowel movements and any symptoms they experience. Patients return to the clinic at least twice a week to receive IL-12 (or placebo) injections. At Weeks 2 and 4, patients are seen by one of the principal investigators. Blood samples are obtained for viral load measurements and CD4 count, as well as routine urinalysis. Patients undergo upper endoscopy with jejunal biopsy and colonoscopy with ileal biopsy between Weeks 2 and 4 of therapy for assays of intestinal cytokine expression. A final clinic visit occurs 12 weeks post-therapy for a physical exam and blood tests.

02

Conditions studied

  • Cryptosporidiosis
  • HIV Infections

Keywords

  • AIDS-Related Opportunistic Infections
  • Cryptosporidiosis
  • Acquired Immunodeficiency Syndrome
  • Azithromycin
  • Paromomycin
  • Interleukin-12
03

In context

Cryptosporidiosis

31 studies on the registry are indexed under Cryptosporidiosis; 7 are open to participants now.

This study's enrollment of 16 is below the median of 40 across 17 interventional studies indexed under Cryptosporidiosis.

Browse Cryptosporidiosis studies →

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID) is the lead sponsor of 2,445 studies on the registry; 182 are open to participants now.

Of its 402 completed or terminated interventional studies of FDA-regulated products, 300 (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
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Patients may be eligible for this study if they:

  • Are HIV-positive.
  • Have a CD4 cell count below 150 cells/mm3.
  • Have been on stable anti-HIV therapy that includes at least 2 nucleoside analogues for at least 4 weeks.
  • Have chronic diarrhea (3 bowel movements a day that are loose or watery, for 5 days per week over 3 weeks).
  • Test positively for Cryptosporidium.
  • Are at least 18 years old.
  • Agree to use effective methods of birth control.

Exclusion criteria

Exclusion Criteria

Patients will not be eligible for this study if they:

  • Have any other active opportunistic (AIDS-related) infection.
  • Require intravenous (IV) fluids.
  • Have a history of an allergy to certain medications, such as colony-stimulating factors (G-CSF or GM-CSF) or a type of antibiotic.
  • Are pregnant.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Masking
Double
Enrollment
16 participants
06

Study locations

1 site
  • Pablo C. Okhuysen
    Houston, Texas 77030, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 14, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00001128
Collaborators
Genetics Institute
First posted
Aug 31, 2001
Primary completion
Jun 2005
Completion
Jun 2005
Last update
Dec 14, 2016

Study contacts

A. Clinton White
principal investigator
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2003. You cannot join it, but the record below documents what was studied.

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Studies of the drugs tested here: Interleukin-12 · Paromomycin · Azithromycin

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