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Protocol For the Treatment of Cryptosporidiosis in AIDS Patients With Diclazuril (R64,433)

Primary Purpose

Cryptosporidiosis, HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diclazuril
Sponsored by
Janssen, LP
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, Diarrhea, diclazuril, Coccidiostats, Acquired Immunodeficiency Syndrome

Eligibility Criteria

12 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Concurrent Medication: Allowed: Patients who require anti-diarrheal medication must have received only one anti-diarrheal medication, loperamide, for at least 7 days prior to study entry. Dose of loperamide cannot be increased during study. Aerosolized pentamidine. Ganciclovir for cytomegalovirus (CMV) retinitis only but patient must be stable at least 4 weeks prior to study entry. Zidovudine (AZT). Nystatin for oropharyngeal infections if not taken within 2 hours of diclazuril. Patients must have: Diagnosis of AIDS that is confirmed HIV positive by Western blot or AIDS defined diagnosis, or CDC defined AIDS. Stool specimens positive for cryptosporidium oocysts. Given written informed consent after the purpose and nature of the study, as well the possible drug-related adverse effects, have been explained. Ability to return for all subsequent applicable visits on days 8, 15, 21, and, if necessary, 28. Prior Medication: Allowed: Aerosolized pentamidine. Loperamide. Ganciclovir for cytomegalovirus (CMV) retinitis. Exclusion Criteria Co-existing Condition: Patients with the following are excluded: Diagnosis of cryptosporidiosis less than 4 weeks prior to study entry, unless patient has been diagnosed with AIDS for more than 4 weeks. Other treatable enteric pathogens including Clostridia must be treated and eradicated prior to study entry. Inability to swallow capsules. Uncontrolled vomiting. Concurrent Medication: Excluded: Trimethoprim/sulfamethoxazole (Bactrim). Ganciclovir for any other reason except cytomegalovirus (CMV) retinitis. Other antibiotics. Other anti-protozoal drugs. Anti-fungal drugs other than nystatin. Amphotericin B. Other investigational drugs. Patients with the following are excluded: Diagnosis of cryptosporidiosis less than 4 weeks prior to study entry, unless patient has been diagnosed with AIDS for more than 4 weeks. Inability to swallow capsules. Uncontrolled vomiting. Life expectancy of < 28 days. Can not be depended upon to follow the instructions of the investigator. Participation in an investigational study within 15 days of study entry. Prior Medication: Excluded within 15 days of study entry: Another investigational drug or device (except aerosolized pentamidine). Prior Treatment: Excluded within 15 days of study entry: Participation in an investigational study.

Sites / Locations

  • Dr Douglas Dieterich
  • Cornell Univ Med Ctr
  • Saint Luke's - Roosevelt Hosp Ctr

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Janssen, LP
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1. Study Identification

Unique Protocol Identification Number
NCT00002027
Brief Title
Protocol For the Treatment of Cryptosporidiosis in AIDS Patients With Diclazuril (R64,433)
Official Title
Protocol For the Treatment of Cryptosporidiosis in AIDS Patients With Diclazuril (R64,433)
Study Type
Interventional

2. Study Status

Record Verification Date
June 1990
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Janssen, LP

4. Oversight

5. Study Description

Brief Summary
To evaluate the safety and efficacy of diclazuril capsules compared with placebo capsules as treatment of cryptosporidial related diarrhea in AIDS patients. Treatment efficacy will be based on the drug's clinical results and on its anti-protozoan effects. Safety will be assessed by the occurrence of side effects as reported by patients at their visits and by frequent monitoring of hematology, biochemistries, and urinalysis.

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, Diarrhea, diclazuril, Coccidiostats, Acquired Immunodeficiency Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Diclazuril

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: Patients who require anti-diarrheal medication must have received only one anti-diarrheal medication, loperamide, for at least 7 days prior to study entry. Dose of loperamide cannot be increased during study. Aerosolized pentamidine. Ganciclovir for cytomegalovirus (CMV) retinitis only but patient must be stable at least 4 weeks prior to study entry. Zidovudine (AZT). Nystatin for oropharyngeal infections if not taken within 2 hours of diclazuril. Patients must have: Diagnosis of AIDS that is confirmed HIV positive by Western blot or AIDS defined diagnosis, or CDC defined AIDS. Stool specimens positive for cryptosporidium oocysts. Given written informed consent after the purpose and nature of the study, as well the possible drug-related adverse effects, have been explained. Ability to return for all subsequent applicable visits on days 8, 15, 21, and, if necessary, 28. Prior Medication: Allowed: Aerosolized pentamidine. Loperamide. Ganciclovir for cytomegalovirus (CMV) retinitis. Exclusion Criteria Co-existing Condition: Patients with the following are excluded: Diagnosis of cryptosporidiosis less than 4 weeks prior to study entry, unless patient has been diagnosed with AIDS for more than 4 weeks. Other treatable enteric pathogens including Clostridia must be treated and eradicated prior to study entry. Inability to swallow capsules. Uncontrolled vomiting. Concurrent Medication: Excluded: Trimethoprim/sulfamethoxazole (Bactrim). Ganciclovir for any other reason except cytomegalovirus (CMV) retinitis. Other antibiotics. Other anti-protozoal drugs. Anti-fungal drugs other than nystatin. Amphotericin B. Other investigational drugs. Patients with the following are excluded: Diagnosis of cryptosporidiosis less than 4 weeks prior to study entry, unless patient has been diagnosed with AIDS for more than 4 weeks. Inability to swallow capsules. Uncontrolled vomiting. Life expectancy of < 28 days. Can not be depended upon to follow the instructions of the investigator. Participation in an investigational study within 15 days of study entry. Prior Medication: Excluded within 15 days of study entry: Another investigational drug or device (except aerosolized pentamidine). Prior Treatment: Excluded within 15 days of study entry: Participation in an investigational study.
Facility Information:
Facility Name
Dr Douglas Dieterich
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Cornell Univ Med Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Saint Luke's - Roosevelt Hosp Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10025
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
2397069
Citation
Connolly GM, Youle M, Gazzard BG. Diclazuril in the treatment of severe cryptosporidial diarrhoea in AIDS patients. AIDS. 1990 Jul;4(7):700-1. doi: 10.1097/00002030-199007000-00020. No abstract available.
Results Reference
background
Citation
Soave R, Dieterich D, Kotler D, Gassyuk E, Tierney AR, Liebes L, Legendre R. Oral diclazuril therapy for cryptosporidiosis. Int Conf AIDS. 1990 Jun 20-23;6(1):252 (abstract no ThB520)
Results Reference
background

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Protocol For the Treatment of Cryptosporidiosis in AIDS Patients With Diclazuril (R64,433)

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