A Study of ART24 in Subjects Recently Cured of a Clostridioides Difficile Infection (CDI)

• Status: Recruiting
• Trial end date: 2023-02-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a randomized, placebo-controlled, double-blind, multi-site study in which up to approximately 36 subjects with a recent C. difficile infection (CDI) who have completed a standard of care course of CDI antibiotics and have achieved clinical cure based on signs and symptoms, will be randomized to 7 or 28 daily doses of ART24 or placebo. Subjects will be followed for 6 months after the last dose of study drug.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Artugen Therapeutics USA, Inc.

Criteria

Inclusion Criteria:

• Have successfully completed a full course of a standard of care CDI antibiotic for a qualifying CDI episode (primary or recurrent) within 3 to 7 days of randomization

• Qualifying CDI episode must meet all of the following (3) criteria

1. Positive stool C. difficile toxin (NAAT, EIA, CCTA, or equivalent test) as documented by study site AND

2. History of ≥3 unformed stools (Bristol scores of 5, 6, or 7) within 24 hours

3. Received standard of care antibiotic treatment for CDI diagnosis

• Prior to the first dose of study drug, completion of standard of care antibiotic therapy with oral vancomycin, metronidazole, or fidaxomicin for CDI with a treatment duration of 10 to 21 days

• Clinical cure assessed at Day 1 visit (randomization) defined as ≤2 unformed stools per day for at least 2 consecutive days and maintained through Day 1 without the need for further antibiotic therapy

• Able to begin treatment with study drug within 3 to 7 days following completion (i.e., last dose) of the CDI antibiotic course for the qualifying CDI episode

Exclusion Criteria:

• Body mass index ≥40.0 kg/m2

• Life expectancy of ≤12 months

• Inpatient (in hospital or skilled nursing facility) at the time of randomization

• Current (i.e., qualifying) CDI episode required admission to an Intensive Care Unit

• Pregnant, breastfeeding, or seeking pregnancy while on study

• Have, as determined by the Investigator, a history or clinical/laboratory manifestations of significant neurological, renal, hepatic, hematologic, cardiac, pulmonary, metabolic, endocrine, psychiatric, GI disorders other than CDI (including infectious, ischemic, or immunological diseases), human immunodeficiency virus (HIV), hepatitis B virus (HBV), and/or hepatitis C virus (HCV) infection, or other condition that could interfere with the evaluation of safety or efficacy, or put the subject at risk of harm from study participation

• Have an active malignancy of any type or history of a malignancy within past 5 years, except for treated basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix

• Have an acute febrile illness (fever >38°C [100.4°F]) at Day 1

• Drug, alcohol, or substance dependence within the last 2 years

• Any of the following laboratory results at Screening:

• White blood cell count ≥15,000 cells/mm3

• Absolute neutrophil count <1000/mm3

• Liver function test result (e.g., aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT), or total bilirubin) of ≥3 times the upper limit of normal

• Serum albumin <3 g/dL

• Serum creatinine >1.8 mg/dL and oliguric

• Use of systemic antibiotic therapy for conditions other than CDI within 7 days of randomization or expectation to require antibiotic therapy for conditions other than CDI for 12 weeks following the first dose of study drug for Cohort A or 16 weeks following the first dose of study drug for Cohort B, including subtherapeutic doses of oral antibiotics (e.g., for rosacea)

• Have a known immunodeficiency disorder, including but not limited to:

• An immunodeficiency disease

• Receiving, or plans to receive, treatment with systemic corticosteroids equivalent to >10 mg prednisone per day

• Receiving, or plans to receive, myelosuppressive chemotherapy

• Previous fecal transplant or live biotherapeutic product within 1 year of randomization

• Treatment with bezlotoxumab (Zinplava™) for the qualifying CDI episode

• Diagnosis of inflammatory bowel disease (including but not limited to: Crohn's disease, ulcerative colitis, microscopic colitis)

• Active irritable bowel syndrome [those with diarrhea predominant or alternating constipation and diarrhea] (in past 6 months based on Rome IV criteria and subject deemed not suitable for study by Investigator's judgment)

• Celiac disease not well controlled on gluten-free diet

• Active gastroparesis, toxic megacolon, pseudomembranous colitis, colostomy, intestinal resection (except appendectomy), ileus or short gut syndrome

• History of chronic diarrhea apart from prior CDI

• Intra-abdominal surgery, including laparoscopic procedures, within 8 weeks of Screening (appendectomy and cholecystectomy excluded)

• History of difficulty swallowing food or liquids

• Taking antidiarrheal agents (e.g., loperamide) or laxatives (e.g., senna) on a regular basis

• Use of non-dietary probiotic supplements within 7 days of Day 1 or plan to use non-dietary probiotic supplements while on study through Week 12 in Cohort A and Week 16 in Cohort B

• Known to have consumed fermented or other foods that may contain B. amyloliquefaciens (such as miso, soybean paste, or fermented rice- or locust bean-derived products) within 7 days prior to Day 1, or plan to consume them prior to Week 12 for Cohort A and prior to Week 16 for Cohort B

• Participation in a clinical trial of an investigational drug or medical device within 30 days or 5 half-lives, whichever is longer, prior to the Screening visit