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A Study of Itraconazole in the Treatment and Prevention of Histoplasmosis, a Fungal Infection, in Patients With AIDS

Primary Purpose

HIV Infections, Histoplasmosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Itraconazole
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 HIV Infections focused on measuring AIDS-Related Opportunistic Infections, Histoplasmosis, Drug Evaluation, Antifungal Agents, Acquired Immunodeficiency Syndrome

Eligibility Criteria

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

Inclusion Criteria Concurrent Medication: Allowed: Vincristine, vinblastine, bleomycin, or interferon for Kaposi's sarcoma. Erythropoietin. Didanosine by exemption for 10 patients. Barbiturates. Coumarin-type anticoagulants. Oral contraceptives. Digoxin. Methadone. Narcotics. Acyclovir. Acetaminophen. Sulfonamides. Trimethoprim / sulfamethoxazole. Pentamidine for Pneumocystis carinii pneumonia (PCP) or PCP prophylaxis. Topical antifungals. Pyrimethamine. Ganciclovir. AZT. Stress doses of steroids in patients with adrenal insufficiency. Concurrent Treatment: Allowed: Dose reduction or interruption of myelosuppressive therapy and transfusion to maintain hemoglobin of 7 or more g/dl. Radiation therapy. Patient must: Show laboratory evidence of HIV infection and disseminated histoplasmosis. Be oriented to person, place, and time. Be able to give written informed consent (appropriate consent must be obtained from a parent or legal guardian for patients under 18 years of age). Allowed: Abnormal liver function tests in Grade 3 toxicity range if liver biopsy shows evidence that histoplasmosis caused these abnormalities. Mucocutaneous candidiasis. Prior Medication: Allowed: Amphotericin B or ketoconazole for pulmonary histoplasmosis at least 3 months prior to study entry. Azidothymidine (AZT). Vincristine, vinblastine, bleomycin, or interferon for mucocutaneous Kaposi's sarcoma. Prophylaxis for Pneumocystis carinii pneumonia (PCP). Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Severely ill, or at risk of dying from histoplasmosis within the first week of treatment, as indicated by systolic blood pressure less than 90 mm Hg , or PO2 less than 60. Active CNS lesions, malignancies, or infections other than MAI. Severe malabsorption syndrome (persistent diarrhea more than 4 weeks duration with at least 4 loose stools per day accompanied by a 10 percent or greater weight loss). Requiring cytotoxic therapy for malignancies. Any systemic fungal infection other than histoplasmosis. Systemic Mycobacterium avium intracellulare. Receiving treatment for other acute opportunistic infections whose signs and symptoms have not yet resolved or stabilized. History of allergy to or intolerance of imidazoles or azoles. Concurrent Medication: Excluded: All other systemic antifungal agents. Investigational drugs not specifically allowed. Oral hypoglycemics. Rifamycins. Phenytoin. Carbamazepine. Steroids in excess of physiologic replacement doses not specifically allowed. Cytotoxic chemotherapy. Discouraged: Antacids. Sucralfate. H2 blockers. Patients with the following are excluded: Severely ill, or at risk of dying from histoplasmosis within the first week of treatment. Active CNS infections, malignancies or lesions not documented to be caused by histoplasmosis, which would interfere with assessment of response. Unable to take oral medications reliably. Severe malabsorption syndrome. Requiring cytotoxic therapy for malignancies. Any systemic fungal infection other than histoplasmosis. Systemic Mycobacterium avium intracellulare. Receiving treatment for other acute opportunistic infections whose signs and symptoms have not yet resolved or stabilized. Prior Medication: Excluded for greater than 1 week within the last 3 months: Fluconazole. Itraconazole. SCH 39304. Amphotericin B greater than 1.5 mg/kg, or any other antifungal for this episode of disseminated histoplasmosis. Patients who the investigator feels would be undependable with regard to adherence to the protocol.

Sites / Locations

  • USC CRS
  • Northwestern University CRS
  • Indiana Univ. School of Medicine, Infectious Disease Research Clinic
  • Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU
  • University of Minnesota, ACTU
  • Washington U CRS
  • Cornell University A2201
  • Univ. of Rochester ACTG CRS
  • Duke Univ. Med. Ctr. Adult CRS
  • Univ. of Cincinnati CRS
  • The Ohio State Univ. AIDS CRS
  • Pitt CRS

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 28, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Janssen Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00000975
Brief Title
A Study of Itraconazole in the Treatment and Prevention of Histoplasmosis, a Fungal Infection, in Patients With AIDS
Official Title
Pilot Study To Determine the Feasibility of Itraconazole for Primary Treatment and Suppression of Relapse of Disseminated Histoplasmosis in Patients With the Acquired Immunodeficiency Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 1994 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Janssen Pharmaceuticals

4. Oversight

5. Study Description

Brief Summary
To evaluate the feasibility of itraconazole as (1) primary therapy in histoplasmosis and (2) maintenance therapy after completion of primary therapy. To evaluate the effect of therapy of CNS histoplasmosis. To determine if resistance to drug occurs in patients who fail therapy. Histoplasmosis is a serious opportunistic infection in patients with AIDS. Although the clinical response to amphotericin B treatment in the AIDS patients is generally good, administration difficulties and toxicity detract from its usefulness. Oral treatment with ketoconazole overcomes these limitations of amphotericin B, but does not appear to be effective for primary treatment in patients with AIDS. Itraconazole is a triazole compound in which preclinical studies have demonstrated activity against Histoplasmosis capsulatum. Preclinical studies have also shown that itraconazole appears effective in the treatment of histoplasmosis. The frequency of adverse reactions to itraconazole has been low in several studies. Central nervous system (CNS) involvement occurs in up to 20 percent of patients with histoplasmosis, and appears to have a poor response to amphotericin B treatment. Itraconazole has been used successfully in a small number of patients with cryptococcal meningitis, supporting a study of its use in CNS histoplasmosis.
Detailed Description
Histoplasmosis is a serious opportunistic infection in patients with AIDS. Although the clinical response to amphotericin B treatment in the AIDS patients is generally good, administration difficulties and toxicity detract from its usefulness. Oral treatment with ketoconazole overcomes these limitations of amphotericin B, but does not appear to be effective for primary treatment in patients with AIDS. Itraconazole is a triazole compound in which preclinical studies have demonstrated activity against Histoplasmosis capsulatum. Preclinical studies have also shown that itraconazole appears effective in the treatment of histoplasmosis. The frequency of adverse reactions to itraconazole has been low in several studies. Central nervous system (CNS) involvement occurs in up to 20 percent of patients with histoplasmosis, and appears to have a poor response to amphotericin B treatment. Itraconazole has been used successfully in a small number of patients with cryptococcal meningitis, supporting a study of its use in CNS histoplasmosis. At least 30 patients with AIDS and an initial episode of disseminated histoplasmosis are selected for this study. Up to 5 patients will have a diagnosis of CNS histoplasmosis. Therapy with all other systemic antifungal agents must be halted before study entry. Patients receive itraconazole for 3 days followed by daily oral doses for a total of 12 weeks. Patients who are doing well clinically, without evidence of clinical failure or dose-limiting toxicity, are permitted to continue maintenance therapy to prevent relapse at a reduced dose for an additional 12 months. Patients who are being treated for CNS histoplasmosis will continue to receive itraconazole.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Histoplasmosis
Keywords
AIDS-Related Opportunistic Infections, Histoplasmosis, Drug Evaluation, Antifungal Agents, Acquired Immunodeficiency Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Itraconazole

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: Vincristine, vinblastine, bleomycin, or interferon for Kaposi's sarcoma. Erythropoietin. Didanosine by exemption for 10 patients. Barbiturates. Coumarin-type anticoagulants. Oral contraceptives. Digoxin. Methadone. Narcotics. Acyclovir. Acetaminophen. Sulfonamides. Trimethoprim / sulfamethoxazole. Pentamidine for Pneumocystis carinii pneumonia (PCP) or PCP prophylaxis. Topical antifungals. Pyrimethamine. Ganciclovir. AZT. Stress doses of steroids in patients with adrenal insufficiency. Concurrent Treatment: Allowed: Dose reduction or interruption of myelosuppressive therapy and transfusion to maintain hemoglobin of 7 or more g/dl. Radiation therapy. Patient must: Show laboratory evidence of HIV infection and disseminated histoplasmosis. Be oriented to person, place, and time. Be able to give written informed consent (appropriate consent must be obtained from a parent or legal guardian for patients under 18 years of age). Allowed: Abnormal liver function tests in Grade 3 toxicity range if liver biopsy shows evidence that histoplasmosis caused these abnormalities. Mucocutaneous candidiasis. Prior Medication: Allowed: Amphotericin B or ketoconazole for pulmonary histoplasmosis at least 3 months prior to study entry. Azidothymidine (AZT). Vincristine, vinblastine, bleomycin, or interferon for mucocutaneous Kaposi's sarcoma. Prophylaxis for Pneumocystis carinii pneumonia (PCP). Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Severely ill, or at risk of dying from histoplasmosis within the first week of treatment, as indicated by systolic blood pressure less than 90 mm Hg , or PO2 less than 60. Active CNS lesions, malignancies, or infections other than MAI. Severe malabsorption syndrome (persistent diarrhea more than 4 weeks duration with at least 4 loose stools per day accompanied by a 10 percent or greater weight loss). Requiring cytotoxic therapy for malignancies. Any systemic fungal infection other than histoplasmosis. Systemic Mycobacterium avium intracellulare. Receiving treatment for other acute opportunistic infections whose signs and symptoms have not yet resolved or stabilized. History of allergy to or intolerance of imidazoles or azoles. Concurrent Medication: Excluded: All other systemic antifungal agents. Investigational drugs not specifically allowed. Oral hypoglycemics. Rifamycins. Phenytoin. Carbamazepine. Steroids in excess of physiologic replacement doses not specifically allowed. Cytotoxic chemotherapy. Discouraged: Antacids. Sucralfate. H2 blockers. Patients with the following are excluded: Severely ill, or at risk of dying from histoplasmosis within the first week of treatment. Active CNS infections, malignancies or lesions not documented to be caused by histoplasmosis, which would interfere with assessment of response. Unable to take oral medications reliably. Severe malabsorption syndrome. Requiring cytotoxic therapy for malignancies. Any systemic fungal infection other than histoplasmosis. Systemic Mycobacterium avium intracellulare. Receiving treatment for other acute opportunistic infections whose signs and symptoms have not yet resolved or stabilized. Prior Medication: Excluded for greater than 1 week within the last 3 months: Fluconazole. Itraconazole. SCH 39304. Amphotericin B greater than 1.5 mg/kg, or any other antifungal for this episode of disseminated histoplasmosis. Patients who the investigator feels would be undependable with regard to adherence to the protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
LJ Wheat
Official's Role
Study Chair
Facility Information:
Facility Name
USC CRS
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Northwestern University CRS
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Indiana Univ. School of Medicine, Infectious Disease Research Clinic
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
University of Minnesota, ACTU
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
Facility Name
Washington U CRS
City
Saint Louis
State/Province
Missouri
Country
United States
Facility Name
Cornell University A2201
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Univ. of Rochester ACTG CRS
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States
Facility Name
Duke Univ. Med. Ctr. Adult CRS
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Univ. of Cincinnati CRS
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45267
Country
United States
Facility Name
The Ohio State Univ. AIDS CRS
City
Columbus
State/Province
Ohio
Country
United States
Facility Name
Pitt CRS
City
Pittsburgh
State/Province
Pennsylvania
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
9358104
Citation
Hecht FM, Wheat J, Korzun AH, Hafner R, Skahan KJ, Larsen R, Limjoco MT, Simpson M, Schneider D, Keefer MC, Clark R, Lai KK, Jacobson JM, Squires K, Bartlett JA, Powderly W. Itraconazole maintenance treatment for histoplasmosis in AIDS: a prospective, multicenter trial. J Acquir Immune Defic Syndr Hum Retrovirol. 1997 Oct 1;16(2):100-7. doi: 10.1097/00042560-199710010-00005.
Results Reference
background
PubMed Identifier
7709945
Citation
Wheat J, Hafner R, Korzun AH, Limjoco MT, Spencer P, Larsen RA, Hecht FM, Powderly W. Itraconazole treatment of disseminated histoplasmosis in patients with the acquired immunodeficiency syndrome. AIDS Clinical Trial Group. Am J Med. 1995 Apr;98(4):336-42. doi: 10.1016/s0002-9343(99)80311-8.
Results Reference
background

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A Study of Itraconazole in the Treatment and Prevention of Histoplasmosis, a Fungal Infection, in Patients With AIDS

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