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Treatment of Chronic Cryptosporidiosis in AIDS Patients
This study has been terminated.
Sponsors and Collaborators: National Institute of Allergy and Infectious Diseases (NIAID)
Genetics Institute
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00001128
  Purpose

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.


Condition Intervention
Cryptosporidiosis
HIV Infections
Drug: Interleukin-12
Drug: Paromomycin sulfate
Drug: Azithromycin

MedlinePlus related topics: AIDS Cryptosporidiosis
Drug Information available for: Azithromycin Interleukin-12 Paromomycin Paromomycin sulfate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Double-Blind, Safety Study
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

Further study details as provided by National Institute of Allergy and Infectious Diseases (NIAID):

Estimated Enrollment: 16
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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
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.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00001128

Locations
United States, Texas
Pablo C. Okhuysen
Houston, Texas, United States, 77030
Sponsors and Collaborators
Genetics Institute
Investigators
Principal Investigator: A. Clinton White
  More Information

Click here for more information about Azithromycin  This link exits the ClinicalTrials.gov site
Haga clic aquí para ver información sobre este ensayo clínico en español.  This link exits the ClinicalTrials.gov site

Study ID Numbers: DAIDS R001
Study First Received: January 17, 2000
Last Updated: September 8, 2008
ClinicalTrials.gov Identifier: NCT00001128  
Health Authority: United States: Federal Government

Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
AIDS-Related Opportunistic Infections
Cryptosporidiosis
Acquired Immunodeficiency Syndrome
Azithromycin
Paromomycin
Interleukin-12

Study placed in the following topic categories:
Protozoan Infections
Opportunistic Infections
Sexually Transmitted Diseases, Viral
Interleukin-12
Gastrointestinal Diseases
Acquired Immunodeficiency Syndrome
Intestinal Diseases
Paromomycin
Immunologic Deficiency Syndromes
Virus Diseases
Cryptosporidiosis
Digestive System Diseases
HIV Infections
Azithromycin
AIDS-Related Opportunistic Infections
Sexually Transmitted Diseases
Parasitic Diseases
Intestinal Diseases, Parasitic
Retroviridae Infections

Additional relevant MeSH terms:
Anti-Infective Agents
RNA Virus Infections
Antiprotozoal Agents
Slow Virus Diseases
Immunologic Factors
Immune System Diseases
Antineoplastic Agents
Coccidiosis
Growth Substances
Physiological Effects of Drugs
Adjuvants, Immunologic
Infection
Angiogenesis Inhibitors
Pharmacologic Actions
Anti-Bacterial Agents
Antiparasitic Agents
Therapeutic Uses
Lentivirus Infections
Protozoan Infections, Animal
Parasitic Diseases, Animal
Growth Inhibitors
Angiogenesis Modulating Agents
Amebicides

ClinicalTrials.gov processed this record on January 15, 2009