A Phase 2A Evaluation of the Safety, Tolerability, Pharmacokinetics, Efficacy of Clofazimine (CFZ) in Cryptosporidiosis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2

Total Enrollment

33 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-12-14

Study Completion Date

2019-07-05

Brief Summary

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This study evaluates the safety, tolerability, pharmacokinetics, and efficacy of treating Cryptosporidiosis in HIV positive patients with Clofazimine. Half of the HIV positive patients with Cryptosporidiosis enrolled will be treated with Clofazimine while the other half will be given placebo. An additional group of HIV positive patients without Cryptosporidium infection or diarrhea will be given Clofazimine to assess the differences in pharmacokinetics between HIV positive patients with and without Cryptosporidiosis and diarrhea.

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Detailed Description

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Cryptosporidiosium infection and diarrhea is a life-threatening infection in children 6-18 months and in immunocompromised patients. However, Nitazoxanide, the only drug approved for treatment of Cryptosporidiosis, showed little-to-no efficacy in HIV positive patients and low efficacy in malnourished children.

Recently, Love MS et al reported that Clofazimine inhibited proliferation of both Cryptosporidium parvum and C. hominis in vitro and reduced shedding in a mouse model of acute C. parvum infection. Clofazimine has been approved for treatment of leprosy for decades and more recently for the treatment of drug-resistant Mycobacterium tuberculosis. Safety and pharmacokinetics of Clofazimine are well documented for a variety of patient populations, but not for HIV positive patients or patients with diarrhea. Thus, this clinical trial seeks to determine the efficacy of 50 or 100 mg of Clofazimine administered 3 times daily for 5 days on fecal shedding of Cryptosporidium oocysts in HIV positive patients, as well as safety, tolerability, and pharmacokinetics in this patient population.

Conditions

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Cryptosporidiosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Parallel assignment, placebo-controlled with later arm for pharmacokinetics

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Double-blind

Study Groups

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Clofazimine

Subjects \>/=50 kg: Clofazimine two 50mg gelatin capsules taken orally every 8 hours for 5 days Subjects \<50 kg: Clofazimine 50mg gelatin capsule taken orally every 8 hours for 5 days

Group Type EXPERIMENTAL

Clofazimine

Intervention Type DRUG

50 or 100 mg micronized Clofazimine suspended in an oil-wax base in a gelatin capsule

Placebo

Placebo gelatin capsule(s) taken orally every 8 hours for 5 days.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Oil-wax in gelatin capsule

Clofazimine, no diarrhea

Subjects \>/=50 kg: Clofazimine two 50mg gelatin capsules taken orally every 8 hours for 5 days Subjects \<50 kg: Clofazimine 50mg gelatin capsule taken orally every 8 hours for 5 days

Group Type EXPERIMENTAL

Clofazimine

Intervention Type DRUG

50 or 100 mg micronized Clofazimine suspended in an oil-wax base in a gelatin capsule

Interventions

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Clofazimine

50 or 100 mg micronized Clofazimine suspended in an oil-wax base in a gelatin capsule

Intervention Type DRUG

Placebo

Oil-wax in gelatin capsule

Intervention Type DRUG

Other Intervention Names

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Lamprene Placebo (for Clofazimine)

Eligibility Criteria

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Inclusion Criteria

* Male or Female, Aged 18-65 years old, HIV positive, Cryptosporidium positive by qPCR.
* HIV infection and on stable anti-retroviral therapy treatment for at least 2 weeks
* Weight \>78 lbs/35.4 kg
* Presents with diarrhea defined as a condition of three or more loose stools per day that has persisted for 3 days or longer
* If female, either not of reproductive potential (post-menopause, or status-post surgical sterilization) or using highly effective contraception (\<1% failure, e.g., intrauterine contraceptive device in place or using injectable contraception) or willing to begin highly effective contraception (probably injectable contraception) and continue for the presumed exposure period of Clofazimine (54 days after initiation of treatment)
* Willing and able to provide signed written informed consent or witnessed oral consent in the case of illiteracy, prior to undertaking any trial-related procedures

Exclusion Criteria

* Any condition for which participation in the study, as judged by the investigator, could compromise the well-being of the subject or prevent, limit or confound protocol specified assessments
* Fever \>38.0˚C at presentation
* Subjects will be screened for evidence of active tuberculosis based on sputum production, fever and chest x-ray. Those with sputum production will be tested by Acid Fast Bacilli stain of sputum smear and/or by GeneXpert testing. Those with positive sputum or chest x-ray suggestive of tuberculosis will be excluded from this study and referred for treatment.
* Is critically ill, or in the judgment of the investigator has a prognosis that could lead to imminent mortality within 60 days or compromise participation in the trial or endanger the subject by entering the trial.
* History of allergy or hypersensitivity to Clofazimine.
* Significant cardiac arrhythmia requiring medication.
* Electrocardiogram exclusions based on the means from triplicate electrocardiograms performed on Day -1:

1. Marked prolongation of QT/QTc interval, e.g., confirmed demonstration of QTcF or QTcB interval \>450 ms
2. Pathological Q waves (defined as \>40 ms or depth \>0.4 to 0.5mV);
3. Electrocardiogram evidence of ventricular pre-excitation
4. Electrocardiogram evidence of complete or incomplete left bundle branch block or right bundle branch block
5. Electrocardiogram evidence of second or third degree heart block
6. Intraventricular conduction delay with QRS duration \>120 ms
7. Bradycardia as defined by sinus rate \<50 bpm.
* History of additional risk factors for Torsade de Pointes, e.g., heart failure; bradycardia with HR\<50 bpm, untreated hypothyroidism, hypokalemia \<3.0 mEq/L
* Family history of long QT syndrome
* Use of concomitant medications that markedly prolong the QT/QTc interval or are predicted to have drug-drug interactions with Clofazimine that may lead to toxicity from the partner drug including Amiodarone, Amprenavir, Atazanavir, Bedaquiline, Bepridil, Chloroquine, Chlorpromazine, Cisapride, Clarithromycin, Cyclobenzaprine, Darunavir, Delamanid, Disopyramide Dofetilide, Domperidone, Droperidol, Erythromycin, Fosamprenavir, Halofantrine, Haloperidol, Ibutilide, Indinavir, Levomethadyl, Lopinavir, Mesoridazine, Methadone, Nelfinavir, Pentamidine, Pimozide, Procainamide, Quinidine, Ritonavir, Simiprinivir, Sotalol, Sparfloxacin, Thioridazine, or Tiprinivir
* Pregnant and lactating women (screening pregnancy test for females and pregnancy test at the discharge follow up visit)
* Use of systemic corticosteroids or anti-cryptosporidial treatments within the 28 days preceding Day -1
* Subjects with clinically significant laboratory value abnormalities at screening including but not limited to (note: exclusionary results may not be returned until after enrollment but should be confirmed by the time of the beginning of administration of study drug):

1. Hemoglobin \<5 g/dL
2. Serum potassium \<3.0 mEq/L
3. Aspartate Aminotransferase or Alanine Aminotransferase ≥3.0 x ULN

Part B:

Same Eligibility Criteria except without diarrhea and is Cryptosporidium negative by qPCR.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No