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First in Human Phase 1 Ascending Dose Study of PanChol in Healthy Volunteers

First in Human Phase 1 Ascending Dose Study of PanChol in Healthy Volunteers

Recruiting
18-55 years
All
Phase 1

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Overview

This study is a first-in-human, Phase 1 study of the safety, tolerability, and immunogenicity of PanChol in healthy volunteers. There will be three modules in this clinical trial assessing dosing, safety, and immunogenicity:

  1. a fixed dose-ranging module,
  2. an adaptive dose-finding/optimization module, and
  3. a placebo-controlled expansion module.

Description

The primary objectives of this study are:

  • To evaluate the reactogenicity and the safety of a single-dose PanChol over a range of doses in healthy volunteers.
  • To evaluate the immunogenicity of a single-dose PanChol over a range of doses as measured by vibriocidal antibody titers.

The secondary objectives of this study are:

  • To further characterize PanChol immune response, such as the magnitude of vibriocidal titers, the IgG, IgA, and IgM antibodies targeting Inaba- and Ogawa-specific polysaccharides, cholera toxin B subunit, and TCP, IgA- and IgG-antibody secreting cell responses (ALS/plasmablast responses) and/or the memory B cell (MBC) response.
  • To characterize the stool shedding of the PanChol organisms after vaccination.
  • To evaluate the changes of the gut microbiota after PanChol vaccination and to compare these changes with cholera-induced changes on microbiota

Participants will be enrolled at the Brigham and Women's Hospital (BWH). For the first days of the trial, participants will be inpatients in BWH, for optimal safety monitoring and for fecal and blood samples collection. PanChol or placebo will be administered on Day 1. On Day 6, participants will be starting doxycycline to eradicate the shedding of the vaccine organisms. On Day 7, those who are no longer excreting PanChol in their stool will be discharged. After discharge, volunteers will return on days 15, 29, 57, and 180 for monitoring of general health, AE assessment, immune responses, and fecal microbiota composition. Approximately 53 adult healthy volunteers are planned to be enrolled in this study if all planned treatment groups are conducted.

Eligibility

Inclusion Criteria:

  1. Healthy adults aged from 18 to 55 years old.
  2. Considered healthy, as judged by the clinical investigator, according to medical history, physical examination, vital signs, screening laboratories, and medication history.
  3. Understanding and agreeing to comply with the study protocol including the inpatient period.
  4. Female participants must be non-pregnant and non-lactating and either
    1. surgically sterile (history of bilateral ligation, bilateral salpingectomy, bilateral oophorectomy, total hysterectomy) or postmenopausal (defined as as amenorrhea for at least 12 consecutive months before screening without an alternative medical cause)
    2. be of child-bearing potential and practicing an acceptable method of contraception or abstaining from all activities that could result in pregnancy for at least 28 days before vaccination until 3 months after receiving the IP.
        Acceptable methods of contraception include barrier methods (such as condom, diaphragm, or
        cervical cap used in conjunction with spermicide), intrauterine device, hormonal
        contraception (that may be taken or administered by oral, intravaginal, transdermal,
        subdermal or IM route), vasectomized partner (the vasectomized partner should be the sole
        partner for that participant).
        Exclusion Criteria:
        Each participant must not meet any of the following exclusion criteria to be eligible for
        enrollment in the study:
          1. Confirmed or suspected immunosuppressive condition, as a result of a disease (e.g.,
             primary immune deficiency, malignancy, HIV infection) or have taken any systemic
             immunosuppressive therapy within 6 months of enrollment.
          2. Pregnant or lactating women
          3. History of gastrointestinal (GI) disorder, such as previous major GI surgery,
             malabsorption, or any chronic GI disorders that would interfere, according to the
             investigator, with the IP.
          4. Acute GI or febrile illness within 7 days of enrollment.
          5. Have any acute or chronic medical condition that, in the opinion of the investigator,
             would make vaccination unsafe or interfere with the evaluation of immune response to
             study vaccination.
          6. History of cholera vaccination
          7. History of cholera infection
          8. Abnormal stool pattern, defined as < 3 or >21 stools per week.
          9. Allergy or intolerance to PanChol or placebo component (sodium bicarbonate, lactose,
             ascorbic acid)
         10. Use of any systemic antibiotics within 1 month of PanChol administration
         11. Receipt of a live vaccine in the previous 4 weeks or planned in the 4 weeks following
             enrollment
         12. Receipt of a killed or subunit (non-live) vaccine in the previous 2 weeks or planned
             in the 2 weeks following enrollment.
         13. Individuals who do not speak English will not be enrolled into this trial. This study
             involves more than minimal risk and no prospect of direct benefit for participants.
             Additionally, a subject who did not speak English may not be able to easily
             communicate safety concerns in a timely fashion to the study investigators
         14. Childcare workers with direct contact with children ≤ 2 years of age
         15. Individuals whose occupation involves handling of food
         16. Healthcare workers who have direct contact with patients who are immunodeficient,
             HIV-positive, or have an unstable medical condition
         17. Use laxatives regularly
         18. Have diarrhea within 48 hours before enrollment
         19. Have a history of hypersensitivity to any of the tetracyclines
         20. Have a history of hypersensitivity to streptomycin or any aminoglycoside due to the
             known cross-sensitivity of patients to drugs in this class.

Study details
    Cholera
    Cholera Vaccine Toxicity

NCT05657782

Brigham and Women's Hospital

27 January 2024

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