AzTrials
AzTrials

ImmunisationPhase 2NCT04242264

Phase 2 Shigella Vaccine and Challenge

A Phase 2 study testing Shigella sonnei strain 53G and WRSs2 in people with Immunisation and Shigella Infection, run by National Institute of Allergy and Infectious Diseases (NIAID) at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This is a trial to evaluate the safety, reactogenicity, immunogenicity and efficacy of a 10^6 cfu dose of an oral live-attenuated S. sonnei vaccine candidate, WRSs2, in up to 120 healthy males and non-pregnant females aged 18-49, inclusive. Read more about this study

Who is it for?
Ages 18 to 49 yearsHealthy volunteers can take part
Conditions the study is for
Immunisation, Shigella Infection
What is being tested?
Shigella sonnei strain 53G and WRSs2
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
69 participants
Where
2 sitesUnited States
Study dates
12 Oct 2022to 8 Jul 2024
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 49 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Provide informed consent prior to initiation of any study procedures.
  • Are able to understand and comply with planned study procedures and be available for all study visits.
  • Is 18-49 years of age inclusive and in sufficiently good health* to be safely enrolled in this study as determined by medical history, medication use, and abbreviated physical exam.
  • Good health is defined by the absence of any exclusionary medical conditions. If the subject has another current, ongoing medical condition, the condition cannot meet any of the following criteria: 1) first diagnosed within 3 months of enrollment; 2) is worsening in terms of clinical outcome in last 6 months; or 3) involves need for medication that may pose a risk to subject's safety or impede assessment of adverse events or immunogenicity if they participate in the study. Topical, nasal, and inhaled medications (with the exception of inhaled corticosteroids as outlined in the Subject Exclusion Criteria, herbals, vitamins, and supplements are permitted.
  • Oral temperature is less than 100.4 degrees Fahrenheit.
  • Pulse is 50 to 100 beats per minute (bpm), inclusive.
Show all 14Show fewer
  • Systolic blood pressure is 90 to 140 mmHg, inclusive.
  • Diastolic blood pressure is 55 to 90 mmHg, inclusive.
  • Females of childbearing potential may enroll if subject has practiced adequate contraception* = / > 30 days prior to enrollment and agrees to continue adequate contraception for the entire study.
  • Child-bearing potential is defined as not sterilized via tubal ligation, bilateral oophorectomy, salpingectomy, hysterectomy, or successful Essure(R) placement (permanent, non-surgical, non-hormonal sterilization) with documented radiological confirmation test at least 90 days after the procedure, and still menstruating or <1 year of the last menses if menopausal.
  • Adequate contraception includes; non-male sexual relationships, abstinence from sexual intercourse with a male partner, monogamous relationship with vasectomized partner who has been vasectomized for 180 days or more prior to the subject enrollment, barrier methods such as condoms or diaphragms with spermicide, effective intrauterine devices, NuvaRing(R), and licensed hormonal methods such as implants, injectables, or oral contraceptives ("the pill").
  • Females of childbearing potential must have a negative urine or serum pregnancy test within 24 hours prior to enrollment.
  • Drug screen for opiates is negative.
  • BMI (Body Mass Index) between 18 and 40kg/m^2.

Who cannot join

  • Have any disease or medical condition that, in the opinion of the site principal investigator or appropriate sub-investigator, is a contraindication to study participation****.
  • Including acute or chronic disease or medical condition that would place the subject at an unacceptable risk of injury, render the subject unable to meet the requirements of the protocol, or may interfere with the evaluation of responses or the subject's successful completion of this trial. These include:
  • History of inflammatory bowel disease (IBD) (including ulcerative colitis, Crohn's disease, indeterminate colitis, or celiac disease).
  • Irritable bowel syndrome (IBS) within the past 12 months or any active uncontrolled gastrointestinal disorders or diseases as assessed by the investigator. Including: symptoms or evidence of active gastritis or gastroesophageal reflux disease, gastric surgery or gastric acid hyper-secretory disorders (e.g., Zollinger-Ellison syndrome), gastrointestinal obstruction, ileus, gastric retention, bowel perforation, toxic colitis, persistent infectious gastroenteritis, persistent or chronic diarrhea of unknown etiology, Clostridium difficile infection.
  • Known active neoplastic disease (Non-melanoma, treated, skin cancers are permitted), a history of any hematologic malignancy, or have used anticancer chemotherapy/radiation therapy (cytotoxic) within 3 years prior to study enrollment.
  • Personal or family history of reactive arthritis.
Show all 33Show fewer
  • Reported history of HIV, Hepatitis B, or Hepatitis C
  • History of immunodeficiency due to congenital or hereditary causes, underlying illness or treatment.
  • Positive serology results for HLA-B27, HIV, HBsAg, or HCV antibodies.
  • Have clinically significant abnormalities as determined by study investigator in other screening laboratory tests, as outlined in the protocol.
  • Have participated in a previous Shigella challenge study or reports having received vaccination for Shigella previously.
  • Have a previously laboratory confirmed case of disease caused by S. sonnei or serology positive (>1:2500) for anti S. sonnei LPS IgG ELISA titer at screening.
  • Has a history of diarrhea in the 14 days prior to enrollment.
  • Have fewer than 3 stools per week or more than 3 stools per day as the usual frequency.
  • Recent history/current use of immunosuppressive/immunomodulating disease therapy.
  • Known hypersensitivity to ciprofloxacin or trimethoprim-sulfamethoxazole; sodium bicarbonate; or any components of vaccine, placebo, or challenge material.
  • Received or plan to receive a licensed live vaccine within 30 days prior to enrollment.
  • Received or plan to receive a licensed, inactivated, Coronavirus disease 2019 (COVID-19) vaccine or an influenza vaccine within +-7 days from receipt of study product.
  • Have a history of severe reactions following previous immunization with any licensed or unlicensed vaccine.
  • Received Ig or other blood products (with exception of Rho D Ig) within 90 days prior to enrollment.
  • Have taken oral or parenteral (including intra-articular) corticosteroids of any dose, or high-dose inhaled corticosteroids**within 30 days prior to enrollment.
  • High-dose defined per age as using inhaled high dose per reference chart Estimated Comparative Daily Dosages https://www.nhlbi.nih.gov/files/docs/guidelines/asthmaqrg.pdf
  • Have taken systemic antibiotics within 7 days prior to enrollment.
  • Have taken prescription and/or OTC medication containing loperamide, acetaminophen, aspirin, ibuprofen, or other non-steroidal anti-inflammatory < / = 48 hours prior to enrollment.
  • Have a history of alcohol or drug abuse within 1 year prior to enrollment.
  • Have been hospitalized for psychiatric illness, history of suicide attempt, or confinement for danger to self or others within 5 years prior to enrollment.
  • Work or plan to work in either a health care setting, day care center, or as a food handler or have known daily contact with individuals with possible increased susceptibility** to Shigella within 14 days after discharge from inpatient challenge.
  • Immunocompromised, elderly persons aged 70 years or more, diapered individuals, persons with disabilities, children < 2 years old, a woman known to be pregnant or nursing, or anyone with diminished immunity. Known daily contact includes contact at home, school, day-care, nursing home, or similar places.
  • Are pregnant, breastfeeding or plan to become pregnant or breastfeed at any given time during the study.
  • Have fever or an acute illness*** as determined by the site principal investigator or appropriate sub-investigator, within 72 hours prior to enrollment.
  • An acute illness which is nearly resolved with only minor residual symptoms remaining is allowable if, in the opinion of the site principal investigator or appropriate sub-investigator, the residual symptoms will not interfere with the ability to assess safety parameters as required by the protocol
  • Received an experimental agent (including vaccine, drug, biologic, device, blood product, or medication, other than from participation in this trial) within 30 days prior to the first study vaccination or expect to receive an investigational product during the study period which might affect safety or assessment of study endpoints.
  • Taking prescription or over-the-counter medication for weight reduction.

Trial locations and contacts

2 sites in 1 country.

United States2 sites

  • Cincinnati Children's Hospital Medical Center Vaccine Research Center

    Cincinnati, Ohio, 45229-3039

  • The Hope Clinic of Emory University

    Decatur, Georgia, 30030-1705

Other trials in United States

About this study

Official title: A Double-Blind Placebo Controlled Randomized Phase 2 Trial to Evaluate the Safety, Reactogenicity and Immunogenicity of a Live-Attenuated Shigella Sonnei Vaccine, WRSs2 and Determine Its Efficacy in a Challenge Model of S. Sonnei 53G in Healthy Adults

This is a trial to evaluate the safety, reactogenicity, immunogenicity and efficacy of a 10^6 cfu dose of an oral live-attenuated S. sonnei vaccine candidate, WRSs2, in up to 120 healthy males and non-pregnant females aged 18-49, inclusive. This is a two-phase study, an outpatient WRSs2 vaccination phase and an inpatient S. sonnei 53G challenge phase. After the initiation of the study, two participants had Grade 3 diarrhea and/or vomiting in the days following vaccination. The vaccination dose was reduced to 5X10^5, enrollment was changed to 2 arms and randomized 2:1 (vaccine: placebo). Participants with morbid obesity were excluded and weight loss medications prohibited. The Primary Objective of this study is to estimate combined vaccine efficacy of 2 doses of WRSs2 (10^6 cfu or 5X10^5 cfu) in preventing shigellosis, following challenge with S. sonnei strain 53G.

Read the detailed description

This is a double-blind, placebo controlled, randomized study to test the safety, reactogenicity, immunogenicity and efficacy of up to a 10^6 cfu dose of an oral live-attenuated S. sonnei vaccine (WRSs2) to protect against shigellosis after a targeted oral challenge with S. sonnei 53G, a virulent strain of S. sonnei. Up to 120 subjects, healthy males and non-pregnant females aged 18-49, will be enrolled and randomized in this study. Using the 10^6 CFU dose, subjects were randomized 1:1:1 into one of three vaccination arms to receive 2 doses of study agent 28 days apart. Arm 1 received 2 doses of WRSs2, Arm 2 received placebo followed by WRSs2 and Arm 3 received 2 doses of placebo. Twenty-eight (+2) days after the second dose of study agent, subjects were admitted to the inpatient unit and given an oral challenge of approximately 1500 cfu of 53G. The goal was to have 90 subjects (30 per arm) receive a challenge dose of 53G. The study duration is approximately 24 months with subject participation duration approximately 8 months.

After the initiation of the study, two participants had Grade 3 diarrhea and/or vomiting in the days following vaccination. The vaccination dose was reduced to 5X10^5, enrollment was changed to 2 arms and randomized 2:1 (vaccine: placebo). Participants with morbid obesity were excluded and weight loss medications prohibited.

The Primary Objective of this study is to estimate combined vaccine efficacy of 2 doses of WRSs2 (10^6 cfu or 5X10^5 cfu) in preventing shigellosis, following challenge with S. sonnei strain 53G. The Secondary Objectives are to:1) Estimate vaccine efficacy of 1 dose of 10^6 cfu, 2 doses of 10^6 cfu, and 2 doses of 5x10^5 cfu of WRSs2 in preventing shigellosis following challenge with S. sonnei strain 53G. 2) Evaluate the safety of WRSs2; 3) Evaluate immune responses following vaccination (immunogenicity) with WRSs2 and after challenge with S. sonnei strain 53G by serum anti-LPS and anti-Invaplex IgG and IgA by ELISA; 4) Determine fecal shedding of S. sonnei after WRSs2 vaccination and 53G challenge by qualitative stool culture.

Being tested
Placebo, Shigella sonnei strain 53G, WRSs2
Keywords
Challenge, Double-blind, Efficacy, Healthy Adults, Immunogenicity, Live-attenuated Shigella sonnei Vaccine, Phase 2 Trial, Placebo-controlled, Protective efficacy, Randomized, Reactogenicity, Safety, Shigella sonnei 53G Challenge, WRSs2
Medical subject headings
Dysentery, Bacillary

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PlaceboOther

    0.9% Sterile Normal Saline, USP

  • Shigella sonnei strain 53GBiological

    1.5 x 10^3 Colony Forming Units (cfu) Shigella sonnei 53G, a virulent strain of wildtype Shigella sonnei

  • WRSs2Biological

    10^6 Colony Forming Units (cfu) dose of an oral live-attenuated Shigella sonnei vaccine candidate derived from a virulent S. sonnei strain Moseley (WRSs2)-a live, attenuated vaccine that has been manufactured under cGMP conditions at the WRAIR PBF

Study groups in NCT04242264
Study groupRoleWhat they receive
Arm 1ExperimentalVaccine: 1 ml of saline containing10^6 or 5X10^5 cfu of the WRSs2 vaccine in 30 ml of sterile normal saline administered orally on Day 1 and Day 29. Challenge: 1 ml of S. sonnei 53G challenge in 30 ml of sterile saline administered orally on Day 57. N=40
Receives: Biological: Shigella sonnei strain 53G; Biological: WRSs2
Arm 2ExperimentalPlacebo + Vaccine: 30 ml of sterile normal saline placebo administered orally on Day 1 and 1 ml of saline containing 10^6 cfu of the WRSs2 vaccine in 30 ml of sterile normal saline administered orally on Day 29. Challenge: 1 ml of S. sonnei 53G challenge in 30ml of sterile saline administered orally on Day 57. N=40
Receives: Other: Placebo; Biological: Shigella sonnei strain 53G; Biological: WRSs2
Arm 3Placebo comparatorPlacebo: 31 ml of sterile normal saline placebo administered orally on Day 1 and Day 29. Challenge: 1 ml of S. sonnei 53G challenge in 30 ml of sterile saline administered orally on Day 57. N=40
Receives: Other: Placebo; Biological: Shigella sonnei strain 53G

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The Proportion of Participants With Shigellosis Following Challenge With Shigella Sonnei 53G Through Day 63 in the Pooled Group of Participants Receiving Two Doses of 10^6 Cfu or 5x10^5 Cfu of WRSs2 Compared to Participants Receiving Two Doses of Placebo.

    Following study vaccination on Days 1 and 29, participants were admitted to an inpatient facility and challenged with Shigella sonnei strain 53G on Day 57. From challenge through Day 63, all stools passed by challenged participants were graded for consistency, all grade 3-5* stools were visually assessed for gross blood, and all gross blood-containing stools were confirmed via hemoccult test. A blinded endpoint review committee of independent Shigella experts determined whether shigellosis occurred for each participant based on number, weight, consistency, and hemoccult-positive status of stools, along with the presence of additional enteric symptoms.

    *Stool consistency was graded according to the following scale: 1 = Normal stool (best outcome); 2 = Soft stool; 3 = Loose stool; 4 = Watery stool; 5 = Rice water (worst outcome).

    Measured: Day 57 through Day 63

Secondary outcomes (20)

  1. The Proportion of Participants With Shigellosis Following Challenge With S. Sonnei 53G Through Day 63 in Participants Receiving 1 Dose of 10^6 Cfu, 2 Doses of 10^6 Cfu, or 2 Doses of 5x10^5 Cfu of WRSs2 Compared to Those Receiving Two Doses of Placebo.

    Following study vaccination on Days 1 and 29, participants were admitted to an inpatient facility and challenged with Shigella sonnei strain 53G on Day 57. From challenge through Day 63, all stools passed by challenged participants were graded for consistency, all grade 3-5* stools were visually assessed for gross blood, and all gross blood-containing stools were confirmed via hemoccult test. A blinded endpoint review committee of independent Shigella experts determined whether shigellosis occurred for each participant based on number, weight, consistency, and hemoccult-positive status of stools, along with the presence of additional enteric symptoms.

    *Stool consistency was graded according to the following scale: 1 = Normal stool (best outcome); 2 = Soft stool; 3 = Loose stool; 4 = Watery stool; 5 = Rice water (worst outcome).

    Measured: Day 57 through Day 65

  2. Number and Percentage of Participants With Solicited Systemic Adverse Events (AEs) Through 7 Days After Each Study Vaccination.

    Systemic solicited adverse events (AEs) were collected pre-vaccination, 90 minutes post-vaccination, and then daily for 7 days after each vaccination using a memory aid and graded on a scale of 0 (none), 1 (mild), 2 (moderate) and 3 (severe). Systemic events include fever, headache, arthralgia, nausea, pain/abdominal cramps, fatigue/malaise, myalgia, anorexia/loss of appetite, chills, vomiting, and diarrhea.

    Measured: Day 1 through Day 8, Day 29 through Day 36

  3. Number and Percentage of Participants With Vaccine-related Unsolicited AEs Through 28 Days Post Last Vaccination

    ICH E6 defines an AE as any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product regardless of its causal relationship to the study treatment. FDA defines an AE as any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related.

    An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of medicinal (investigational) product. The occurrence of an AE may come to the attention of study personnel during study visits and interviews of a study recipient presenting for medical care, or upon review by a study monitor.

    An AE is considered related if there is a reasonable possibility that the study product caused the AE. Reasonable possibility means that there is evidence to suggest a causal relationship between the study product and the AE.

    Measured: Day 1 through Day 57

  4. Number and Percentage of Participants With SAEs Through Study Day 180 or Until Resolution or Stabilization Even if This Extends Beyond the Study-reporting Period.

    An AE or suspected adverse reaction is considered "serious" if, in the view of either the investigator or sponsor, it results in any of the following outcomes:

    • Death
    • A life-threatening AE
    • Inpatient hospitalization or prolongation of existing hospitalization
    • A persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions
    • A congenital anomaly/birth defect
    • Important medical events that may not result in death, be life-threatening, or require hospitalizations may be considered serious when, based upon appropriate medical judgment they may jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the outcomes listed in this definition.

    Measured: Day 1 through Day 180

  5. Number of Participants With >=4-fold Rise From Pre-vaccination in Anti-LPS (Lipopolysaccharide) IgG (Immunoglobulin G)

    Serum was collected pre-challenge at Day 1 (pre-dose 1), Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgG antibody response against LPS (a Shigella sonnei antigen) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-vaccination day as compared to pre-dose 1 is reported.

    Measured: Day 15, Day 29, Day 43, and Day 56

  6. Number of Participants With >=4-fold Rise From Pre-vaccination in Anti-Invaplex IgG (Immunoglobulin G)

    Serum was collected pre-challenge at Day 1 (pre-dose 1), Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgG antibody response against Invaplex (a Shigella sonnei antigen complex) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-vaccination day as compared to pre-dose 1 is reported.

    Measured: Day 15, Day 29, Day 43, and Day 56

  7. Number of Participants With >=4-fold Rise From Pre-vaccination in Anti-LPS (Lipopolysaccharide) IgA (Immunoglobulin A)

    Serum was collected pre-challenge at Day 1 (pre-dose 1), Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgA antibody response against LPS (a Shigella sonnei antigen) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-vaccination day as compared to pre-dose 1 is reported.

    Measured: Day 15, Day 29, Day 43, and Day 56

  8. Number of Participants With >=4-fold Rise From Pre-vaccination in Anti-Invaplex IgA (Immunoglobulin A)

    Serum was collected pre-challenge at Day 1 (pre-dose 1), Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgA antibody response against Invaplex (a Shigella sonnei antigen complex) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-vaccination day as compared to pre-dose 1 is reported.

    Measured: Day 15, Day 29, Day 43, and Day 56

  9. Maximum Anti-LPS (Lipopolysaccharide) and Anti-Invaplex Serum IgG (Immunoglobulin G) and IgA (Immunoglobulin A) Titer Post-vaccination Through Day 56

    Serum was collected post-vaccination and pre-challenge at Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgG and IgA antibody responses against LPS and Invaplex (Shigella sonnei antigens) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The maximum titer per participant between first vaccination (Day 1) and challenge (Day 57) is summarized by study arm via geometric mean and 95% confidence interval.

    Measured: Day 15 through Day 56

  10. Peak Fold-rise From Pre-vaccination in Anti-LPS (Lipopolysaccharide) and Anti-Invaplex Serum IgG (Immunoglobulin G) and IgA (Immunoglobulin A) Titer

    Serum was collected post-vaccination and pre-challenge at Day 15 (post-dose 1), Day 29 (pre-dose 2), Day 43 (post-dose 2), and Day 56 (post-dose 2) to assess IgG and IgA antibody responses against LPS and Invaplex (Shigella sonnei antigens) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The peak fold-rise is calculated per participant at the maximum titer value post-vaccination (and before challenge) compared to pre-vaccination and is summarized by study arm via geometric mean fold-rise and 95% confidence interval.

    Measured: Day 15 through Day 56

  11. Number of Participants With >=4-fold Rise From Pre-challenge in Anti-LPS (Lipopolysaccharide) IgG (Immunoglobulin G)

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgG antibody response against LPS (a Shigella sonnei antigen) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-challenge day as compared to pre-challenge is reported.

    Measured: Day 64, Day 71, Day 85, and Day 113

  12. Number of Participants With >=4-fold Rise From Pre-challenge in Anti-Invaplex IgG (Immunoglobulin G)

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgG antibody response against Invaplex (a Shigella sonnei antigen complex) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-challenge day as compared to pre-challenge is reported.

    Measured: Day 64, Day 71, Day 85, and Day 113

  13. Number of Participants With >=4-fold Rise From Pre-challenge in Anti-LPS (Lipopolysaccharide) IgA (Immunoglobulin A)

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgA antibody response against LPS (a Shigella sonnei antigen) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-challenge day as compared to pre-challenge is reported.

    Measured: Day 64, Day 71, Day 85, and Day 113

  14. Number of Participants With >=4-fold Rise From Pre-challenge in Anti-Invaplex IgA (Immunoglobulin A)

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgA antibody response against Invaplex (a Shigella sonnei antigen complex) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The number of participants with at least a 4-fold rise in antibody titer on each post-challenge day as compared to pre-challenge is reported.

    Measured: Day 64, Day 71, Day 85, and Day 113

  15. Maximum Anti-LPS (Lipopolysaccharide) and Anti-Invaplex Serum IgG (Immunoglobulin G) and IgA (Immunoglobulin A) Titer Post-challenge Through Day 113

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgG and IgA antibody responses against LPS and Invaplex (Shigella sonnei antigens) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The maximum titer per participant between challenge (Day 57) and Day 113 is summarized by study arm via geometric mean and 95% confidence interval.

    Measured: Day 64 through Day 113

  16. Peak Fold-rise From Pre-challenge in Anti-LPS (Lipopolysaccharide) and Anti-Invaplex Serum IgG (Immunoglobulin G) and IgA (Immunoglobulin A) Titer

    Serum was collected post-challenge at Days 64, 71, 85, and 113 to assess IgG and IgA antibody responses against LPS and Invaplex (Shigella sonnei antigens) as measured by Enzyme Linked ImmunoSorbent Assay (ELISA). The peak fold-rise is calculated per participant at the maximum titer value post-challenge compared to pre-challenge and is summarized by study arm via geometric mean fold-rise and 95% confidence interval.

    Measured: Day 64 through Day 113

  17. Number of Participants Shedding Vaccine Strain in Their Stool by Culture Prior to Challenge

    Stool samples collected at baseline and on Days 4, 8, 15, 29, 32, 36, 43, and 56 were cultured for shedding of Shigella sonnei. For this outcome measure, "baseline" is considered the last day at which culture results were available pre-vaccination (may be at screening visit or Day 1). In the event a subject was unable to produce a bulk stool, rectal swabs were collected for culture.

    Measured: Baseline (day of last culture prior to dose 1) through Day 56

  18. Number of Participants Shedding 53G in Their Stool by Culture Post-challenge

    Stool samples collected on Day 57 (post-challenge) through Day 65 were cultured for shedding of Shigella sonnei strain 53G. In the event a subject was unable to produce a bulk stool, rectal swabs were collected for culture.

    Measured: Day 57 (post-challenge) through Day 65

  19. Mean Duration of Shedding Vaccine Strain Post-vaccination Through Day 56 by Culture.

    Stool samples collected on Day 1 (post-vaccination) and on Days 4, 8, 15, 29, 32, 36, 43, and 56 were cultured for shedding of Shigella sonnei. In the event a subject was unable to produce a bulk stool, rectal swabs were collected for culture.

    The duration of shedding is evaluated from the day of the initial positive culture result to the day of the last positive qualitative or quantitative culture, regardless of intermittent negative results.

    Measured: Day 1 (post-vaccination) through Day 56

  20. Mean Duration of Shedding 53G Post-challenge Through Day 65 by Culture.

    Stool samples collected on Day 57 (post-challenge) through Day 65 were cultured for shedding of Shigella sonnei strain 53G. In the event a subject was unable to produce a bulk stool, rectal swabs were collected for culture.

    The duration of shedding is evaluated from the day of the initial positive culture result to the day of the last positive qualitative or quantitative culture, regardless of intermittent negative results.

    Measured: Day 57 (post-challenge) through Day 65

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2020
  2. Study start12 Oct 2022
  3. Primary completion11 Mar 2024
  4. Study completion8 Jul 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
69 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04242264
Sponsor's protocol ID
17-0112
Status last verified
7 Dec 2023
First submitted
23 Jan 2020
Last updated
10 Aug 2026
FDA-regulated drug
Yes
FDA-regulated device
No

Publications

  • Rouphael N, Baqar S, Dickey M, Quigley C, Pham T, Adams J, Kwatra G, Bechnak S, Smith V, Scherer EM, Graciaa DS, El-Khorazaty J, Fraser JA, Heard S, Cato K, Mejia-Galvis J, Barnoy S, Chandrasekharan L, Porter CK, Suvarnapunya AE, Venkatesan MM, Frenck RW Jr; DMID 17-0112 Study Group. Efficacy of WRSs2, a live-attenuated Shigella sonnei vaccine, against shigellosis in a controlled human infection model in the USA: a phase 2, double-blind, randomised, placebo-controlled trial. Lancet Infect Dis. 2026 Jun 30:S1473-3099(26)00224-0. doi: 10.1016/S1473-3099(26)00224-0. Online ahead of print.

    PubMed 42379208

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Shigella sonnei strain 53G and WRSs2 in people with Immunisation and Shigella Infection, run by National Institute of Allergy and Infectious Diseases (NIAID) at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 14 inclusion and 33 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 24 Apr 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The Proportion of Participants With Shigellosis Following Challenge With Shigella Sonnei 53G Through Day 63 in the Pooled Group of Participants Receiving Two Doses of 10^6 Cfu or 5x10^5 Cfu of WRSs2 Compared to Participants Receiving Two Doses of Placebo. (time frame: Day 57 through Day 63). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04242264, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Aug 2026.

AzTrials uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in