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Treatment of Chronic Cryptosporidiosis in AIDS Patients

Primary Purpose

Cryptosporidiosis, HIV Infections

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Interleukin-12
Paromomycin sulfate
Azithromycin
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cryptosporidiosis focused on measuring AIDS-Related Opportunistic Infections, Cryptosporidiosis, Acquired Immunodeficiency Syndrome, Azithromycin, Paromomycin, Interleukin-12

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 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.

Sites / Locations

  • Pablo C. Okhuysen

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 17, 2000
Last Updated
December 13, 2016
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Genetics Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00001128
Brief Title
Treatment of Chronic Cryptosporidiosis in AIDS Patients
Official Title
A Pilot, Proof-of-Concept, Dose-Escalating Trial of Recombinant Human Interleukin-12 (rhIL-12) Versus Placebo Along With Paromomycin and Azithromycin for Chronic Cryptosporidiosis in AIDS
Study Type
Interventional

2. Study Status

Record Verification Date
June 2003
Overall Recruitment Status
Terminated
Study Start Date
undefined (undefined)
Primary Completion Date
June 2005 (Actual)
Study Completion Date
June 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Genetics Institute

4. Oversight

5. Study Description

Brief 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cryptosporidiosis, HIV Infections
Keywords
AIDS-Related Opportunistic Infections, Cryptosporidiosis, Acquired Immunodeficiency Syndrome, Azithromycin, Paromomycin, Interleukin-12

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
Double
Enrollment
16 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Interleukin-12
Intervention Type
Drug
Intervention Name(s)
Paromomycin sulfate
Intervention Type
Drug
Intervention Name(s)
Azithromycin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
A. Clinton White
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pablo C. Okhuysen
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Treatment of Chronic Cryptosporidiosis in AIDS Patients

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