Overview
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.
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.
Eligibility
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:
1. Age 18 to 50 years old.
2. Body mass index (BMI) of ≥19 kg/m2 to ≤40 kg/m2.
3. 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.
4. 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.
5. 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).
6. Agrees not to donate blood or blood products during participation in the study or for
30 days after completion of study participation.
7. Has negative serology results for HIV, hepatitis B surface antigen (HBsAg), and
hepatitis C virus (HCV) antibody.
8. 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.
9. 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:
1. Barrier method (such as condoms, diaphragm, or cervical cap) used in conjunction
with spermicide and another method, such as prescription hormonal contraceptive;
2. Intrauterine device (IUD);
3. Prescription hormonal contraceptive taken or administered via oral (pill),
transdermal (patch) subdermal, or intramuscular route used in combination with
another method, such as barrier methods;
4. Total abstinence;
5. Sterilization of a monogamous female participant's male partner prior to entry
into the study.
Note: periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation
methods) and withdrawal are not acceptable methods of contraception.
10. 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.
11. 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:
1. Investigational research agents received within 30 days before first treatment.
2. Pregnant or breastfeeding.
3. Regular (no more than once a week) use of antidiarrheals, stool softeners, laxatives,
antacids, or other agents to lower stomach acidity.
4. Use of oral or intravenous antimicrobials within 2 weeks of study start or planned use
during active study phase. Topical treatments are allowed.
5. Proton pump inhibitors, H2 blockers or antacids within 48 hours prior to dosing or
planned use during active study phase.
6. Abnormal bowel patterns, defined by <3 stools per week or >2 stools per day on average
over the past 6 months.
7. 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.
8. 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.
9. History of myocarditis, pericarditis, cardiomyopathy, congestive heart failure with
permanent sequelae, clinically significant arrhythmia (including any arrhythmia
requiring medication, treatment, or clinical follow-up).
10. 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:
1. Any contraindication to repeated blood draws;
2. A condition or process for which signs or symptoms could be confused with
reactions to treatment;
3. Any of the following in the past 10 years: Crohn's disease, ulcerative colitis,
irritable bowel disease, celiac disease, stomach, or intestinal ulcers, or 2 or
more episodes of inflammatory arthritis (joint pain and swelling);
4. Bacterial infection at time of enrollment;
5. Blood in stool on >2 occasions (other than small amounts from straining) in past
12 months;
6. Recurrent diarrhea (>5 episodes in past 6 months, each lasting >3 days or more).
11. History of excessive alcohol consumption or drug dependence within last 3 years.
12. 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.
13. 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.
14. Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or
platelet disorder requiring special precautions).
15. 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).
16. 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.
17. Asplenia: any condition resulting in the absence of a functional spleen.
18. 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).
19. 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.
20. 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:
1. Age 18 to 50 years old.
2. BMI of ≥19 kg/m2 to ≤40 kg/m2.
3. 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.
4. 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.
5. Agrees not to donate blood or blood products during participation in the study or for
30 days after completion of study participation.
6. Has negative serology results for HIV, HBsAg, and HCV antibody.
7. 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.
8. Able to tolerate and take oral medication at time of randomization.
9. 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.
10. 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.
1. 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:
2. Barrier method (such as condoms, diaphragm, or cervical cap) used in conjunction
with spermicide and another method, such as prescription hormonal contraceptive;
3. IUD;
4. Prescription hormonal contraceptive taken or administered via oral (pill),
transdermal (patch) subdermal, or intramuscular route used in combination with
another method, such as barrier methods;
5. Total abstinence;
6. Sterilization of a monogamous female participant's male partner prior to entry
into the study.
Note: periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation
methods) and withdrawal are not acceptable methods of contraception.
11. 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.
12. 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:
1. Investigational research agents received within 30 days before first treatment.
2. Pregnant or breastfeeding.
3. Regular (no more than once a week) use of antidiarrheals, stool softeners, laxatives,
antacids, or other agents to lower stomach acidity.
4. Use of oral or intravenous antimicrobials within 2 weeks of study start or planned use
during active study phase. Topical treatments are allowed.
5. Proton pump inhibitors, H2 blockers or antacids within 48 hours prior to dosing or
planned use during active study phase.
6. Abnormal bowel patterns, defined by <3 stools per week or >2 stools per day on average
over the past 6 months.
7. 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.
8. Taking supplemental probiotics in the form of pills or tablets within 2 weeks.
9. History of myocarditis, pericarditis, cardiomyopathy, congestive heart failure with
permanent sequelae, clinically significant arrhythmia (including any arrhythmia
requiring medication, treatment, or clinical follow-up).
10. 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:
1. Any contraindication to repeated blood draws;
2. A condition or process for which signs or symptoms could be confused with
reactions to treatment;
3. Any of the following in the past 10 years: Crohn's disease, ulcerative colitis,
irritable bowel disease, celiac disease, stomach, or intestinal ulcers;
4. Blood in stool on >2 occasions (other than small amounts from straining) in past
12 months;
5. Recurrent diarrhea (>5 episodes in past 6 months, each lasting >3 days or more);
6. Requires hemodialysis.
11. History of excessive alcohol consumption or drug dependence within last 3 years.
12. 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.
13. 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.
14. Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or
platelet disorder requiring special precautions).
15. 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).
16. 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.
17. Asplenia: any condition resulting in the absence of a functional spleen.
18. 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).
19. Known allergy or hypersensitivity to an excipient in the study drug or placebo.
20. Patients with active infection, a systemic infection requiring treatment, or any other
unstable medical condition that could interfere with the study objectives.
21. 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.