Completed

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

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What is being tested

Diclazuril

Drug
Who is being recruted

Blood-Borne Infections+30

+ Urogenital Diseases

+ Genital Diseases

From 12 to 65 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
See protocol details

Summary

Principal SponsorJanssen, LP
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

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.

NCT00002027
Principal SponsorJanssen, LP
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

60 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 12 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood-Borne InfectionsUrogenital DiseasesGenital DiseasesAnimal DiseasesCoccidiosisCommunicable DiseasesDigestive System DiseasesGastrointestinal DiseasesImmunologic Deficiency SyndromesImmune System DiseasesInfectionsIntestinal DiseasesIntestinal Diseases, ParasiticOpportunistic InfectionsParasitic DiseasesParasitic Diseases, AnimalProtozoan InfectionsProtozoan Infections, AnimalRetroviridae InfectionsRNA Virus InfectionsSexually Transmitted DiseasesSigns and SymptomsSigns and Symptoms, DigestiveSlow Virus DiseasesPathological Conditions, Signs and SymptomsVirus DiseasesSexually Transmitted Diseases, ViralLentivirus InfectionsAcquired Immunodeficiency SyndromeCryptosporidiosisDiarrheaHIV InfectionsAIDS-Related Opportunistic Infections

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.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 3 locations

Dr Douglas Dieterich

New York, United StatesOpen Dr Douglas Dieterich in Google Maps

Cornell Univ Med Ctr

New York, United States

Saint Luke's - Roosevelt Hosp Ctr

New York, United States
Completed3 Study Centers