Status and phase
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Treatments
About
The study is a first-in-human Phase 1/2a randomized, double-blind, placebo-controlled trial to assess the clinical safety and efficacy of VRELysin in healthy and VRE-colonized adults.
Full description
The purpose of this study is to determine if VRELysin is safe and effective in adults in a continuous Phase 1/2a trial. Phase 1 will asses the safety of VRELysin in healthy adults, while Phase 2a will evaluate the safety and efficacy of VRELysin in adults colonized with VRE in the gastrointestinal tract.
VRELysin is a collection of bacteriophages. Bacteriophages (or phages) are viruses that infect only bacteria. The phages in VRELysin infect a specific type of bacteria called Enterococcus, which can cause gastrointestinal infections. VRELysin is intended to significantly reduce or eliminate vancomycin-resistant Enterococcus (VRE) levels in the human gastrointestinal tract, which in turn, may prevent subsequent infection as well as nosocomial spread.
Enrollment
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Inclusion and exclusion criteria
PHASE 1 INCLUSION CRITERIA:
To be eligible to participate in the Phase 1 segment of the study, each subject must fulfill ALL of the following criteria:
Age 18 to 50 years old.
Body mass index (BMI) of ≥19 kg/m2 to ≤40 kg/m2.
Has the ability to understand the study procedures and risks involved with the study, voluntarily agrees to participate by giving written informed consent and is willing to adhere to dose and visit schedules. The subject must be able to read, understand, and complete questionnaires and memory aids.
Agrees not to enroll in another study of an investigational research agent during the study, with the exception of potentially lifesaving or coronavirus disease of 2019 (COVID-19)-related experimental treatments.
Good general health as shown by medical history, physical examination, and screening laboratory tests or clinical laboratory abnormalities per clinical judgment of Principal Investigator (PI).
Agrees not to donate blood or blood products during participation in the study or for 30 days after completion of study participation.
Has negative serology results for HIV, hepatitis B surface antigen (HBsAg), and hepatitis C virus (HCV) antibody.
Female subjects must have a negative serum or urine beta human chorionic gonadotropin (β-HCG) pregnancy test at Screening and within 24 hours of initial treatment on Day 1.
a. Persons who are NOT of reproductive potential due to having undergone total hysterectomy or bilateral oophorectomy (verified by medical records) are not required to undergo pregnancy testing.
Female subjects of reproductive potential must agree to use adequate contraception, defined as consistent and correct use of an FDA-recommended contraceptive method or combination of methods in accordance with the product label. For example:
Note: periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
Female subjects must also agree not to seek pregnancy through alternative methods, such as artificial insemination or in vitro fertilization until after the last required study visit is completed.
Male subjects must agree to use adequate contraception, defined as consistent and correct use of an FDA-recommended contraceptive method in accordance with the product label (see above), for the duration of the study and refrain from donating sperm during this period.
PHASE 1 EXCLUSION CRITERIA:
To be eligible to participate in Phase 1, subjects must NOT fulfill ANY of the following criteria:
Investigational research agents received within 30 days before first treatment.
Pregnant or breastfeeding.
Regular (no more than once a week) use of antidiarrheals, stool softeners, laxatives, antacids, or other agents to lower stomach acidity.
Use of oral or intravenous antimicrobials within 2 weeks of study start or planned use during active study phase. Topical treatments are allowed.
Proton pump inhibitors, H2 blockers or antacids within 48 hours prior to dosing or planned use during active study phase.
Abnormal bowel patterns, defined by <3 stools per week or >2 stools per day on average over the past 6 months.
History of diarrhea in the 7 days prior to treatment. Outpatient diarrhea is defined as ≥ 3 unformed (Grade 3 or greater) loose stools in 24 hours.
Use of oral supplemental probiotics in the form of pills or tablets within 2 weeks of study start or planned use during active study phase.
History of myocarditis, pericarditis, cardiomyopathy, congestive heart failure with permanent sequelae, clinically significant arrhythmia (including any arrhythmia requiring medication, treatment, or clinical follow-up).
Clinically significant medical condition, physical examination findings, clinically significant abnormal laboratory results, or past medical history with clinically significant implications for current health. A clinically significant condition or process includes, but is not limited to:
History of excessive alcohol consumption or drug dependence within last 3 years.
Any medical, psychiatric, occupational, or other condition that, in the judgment of the investigator, would interfere with, or serve as a contraindication to, protocol adherence, assessment of safety, or a subject's ability to give informed consent.
Psychiatric condition that precludes compliance with the protocol. Specifically excluded are persons with psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years.
Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions).
Malignancy (Not excluded from participation: subject who has had malignancy excised surgically and who, in the investigator's estimation, has a reasonable assurance of sustained cure, or who is unlikely to experience recurrence of malignancy during the period of the study).
Seizure disorder/epilepsy: History of seizure(s) within past 3 years. Also exclude if subject has used medications in order to prevent or treat seizure(s) at any time within the past 3 years.
Asplenia: any condition resulting in the absence of a functional spleen.
History of chronic gastrointestinal illness, including severe dyspepsia, lactose intolerance, or other significant gastrointestinal tract disease (e.g., irritable bowel syndrome/disease, inflammatory bowel syndrome, gastric ulcer disease, Crohn's disease).
Any other criteria which, in the Investigator's opinion, would compromise the ability of the subject to participate in the study, the safety of the study, or the results of the study.
Known allergy or hypersensitivity to an excipient in the study drug or placebo.
PHASE 2A INCLUSION CRITERIA:
To be eligible to participate in the Phase 2a segment of the study, each subject must fulfill ALL of the following criteria:
Age 18 to 50 years old.
BMI of ≥19 kg/m2 to ≤40 kg/m2.
Has the ability to understand the study procedures and risks involved with the study, voluntarily agrees to participate by giving written informed consent and is willing to adhere to dose and visit schedules. The subject must be able to read, understand, and complete questionnaires and memory aids.
Agrees not to enroll in another study of an investigational research agent during the study, with the exception of potentially lifesaving or COVID-19-related experimental treatments.
Agrees not to donate blood or blood products during participation in the study or for 30 days after completion of study participation.
Has negative serology results for HIV, HBsAg, and HCV antibody.
Has 2 consecutive positive VRE stool cultures (at least 7 days apart) that are susceptible to VRELysin. The second stool culture must be within 7 days of randomization.
Able to tolerate and take oral medication at time of randomization.
Female subjects must have a negative serum or urine β-HCG pregnancy test at Screening and within 24 hours of initial treatment on Day 1.
Persons who are NOT of reproductive potential due to having undergone total hysterectomy or bilateral oophorectomy (verified by medical records) are not required to undergo pregnancy testing.
Note: periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
Female subjects must also agree not to seek pregnancy through alternative methods, such as artificial insemination or in vitro fertilization until after the last required study visit is completed.
Male subjects must agree to use adequate contraception, defined as consistent and correct use of an FDA-recommended contraceptive method in accordance with the product label (see above), for the duration of the study and refrain from donating sperm during this period.
PHASE 2A EXCLUSION CRITERIA:
To be eligible to participate in Phase 2a, subjects must NOT fulfill ANY of the following criteria:
Investigational research agents received within 30 days before first treatment.
Pregnant or breastfeeding.
Regular (no more than once a week) use of antidiarrheals, stool softeners, laxatives, antacids, or other agents to lower stomach acidity.
Use of oral or intravenous antimicrobials within 2 weeks of study start or planned use during active study phase. Topical treatments are allowed.
Proton pump inhibitors, H2 blockers or antacids within 48 hours prior to dosing or planned use during active study phase.
Abnormal bowel patterns, defined by <3 stools per week or >2 stools per day on average over the past 6 months.
History of diarrhea in the 7 days prior to treatment. Outpatient diarrhea is defined as ≥3 unformed (Grade 3 or greater) loose stools in 24 hours.
Taking supplemental probiotics in the form of pills or tablets within 2 weeks.
History of myocarditis, pericarditis, cardiomyopathy, congestive heart failure with permanent sequelae, clinically significant arrhythmia (including any arrhythmia requiring medication, treatment, or clinical follow-up).
Clinically significant medical condition, physical examination findings, clinically significant abnormal laboratory results, or past medical history with clinically significant implications for current health. A clinically significant condition or process includes but is not limited to:
History of excessive alcohol consumption or drug dependence within last 3 years.
Any medical, psychiatric, occupational, or other condition that, in the judgment of the investigator, would interfere with, or serve as a contraindication to, protocol adherence, assessment of safety, or a subject's ability to give informed consent.
Psychiatric condition that precludes compliance with the protocol. Specifically excluded are persons with psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years.
Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions).
Malignancy (Not excluded from participation: subject who has had malignancy excised surgically and who, in the investigator's estimation, has a reasonable assurance of sustained cure, or who is unlikely to experience recurrence of malignancy during the period of the study).
Seizure disorder/epilepsy: History of seizure(s) within past 3 years. Also exclude if subject has used medications in order to prevent or treat seizure(s) at any time within the past 3 years.
Asplenia: any condition resulting in the absence of a functional spleen.
History of chronic gastrointestinal illness, including severe dyspepsia, lactose intolerance, or other significant gastrointestinal tract disease (e.g., irritable bowel syndrome, inflammatory bowel syndrome, gastric ulcer disease).
Known allergy or hypersensitivity to an excipient in the study drug or placebo.
Patients with active infection, a systemic infection requiring treatment, or any other unstable medical condition that could interfere with the study objectives.
Any other criteria which, in the Investigator's opinion, would compromise the ability of the subject to participate in the study, the safety of the study, or the results of the study.
Primary purpose
Allocation
Interventional model
Masking
80 participants in 2 patient groups, including a placebo group
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Central trial contact
Ellie Morell; Sarah Snook
Data sourced from clinicaltrials.gov
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