Cholera VaccinationPhase 4NCT07487077
Extended Dosing Intervals Trial for Oral Cholera Vaccine, Kenya
A Phase 4 study testing Euvichol-S Oral Cholera Vaccine in people with Cholera Vaccination, run by Albert B. Sabin Vaccine Institute at 1 site in Kenya.
Trial summary
Background: Despite efforts to control cholera, outbreaks continue to occur in Kenya. Oral cholera vaccines (OCVs) are a critical tool in cholera prevention strategies. This study evaluates the immunogenicity of extended dosing intervals for Euvichol-S, a WHO-prequalified OCV, in a Phase IV non-inferiority trial. Read more about this study
- Who is it for?
- Ages 1 year and olderHealthy volunteers can take part
- Conditions the study is for
- Cholera Vaccination
- What is being tested?
- Euvichol-S Oral Cholera Vaccine
- Type of treatment
- Vaccines, Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,071 participants
- Where
- 1 siteKenya
- Study dates
- 31 Oct 2025to Jun 2028
- Phase
- Phase 4
- Are there results?
- Not yet: the study is under way
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 1 year and older
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- Residents of Mukuru, Nairobi, Kenya
- Individuals aged 1 year and above
- Voluntary written informed consent for study participation provided by an individual or his/her legally acceptable representative. Children aged 13 years and above will also provide assent, with parental permission required for all children.
- Ability to comply with study requirements and attend follow-up visits during the study period.
- Participants must be in good health, as determined by medical history, physical examination, and the clinical judgment of the investigators. Clinical judgment will consider factors such as the absence of acute illness or, uncontrolled or severe chronic conditions that may affect participation in the study.
- Lactating women may be enrolled following clinical assessment and informed consent. The vaccine contains killed, formalin-inactivated bacteria that are not systemically absorbed and act locally in the gastrointestinal tract.
Who cannot join
- Known history of hypersensitivity reactions to other vaccines.
- Pregnant women, due to differences in immune response. A pregnancy test will be administered to all female participants who have reached menarche and are under 50 years.
- Reported diarrhea or abdominal pain lasting 2 weeks or longer within 6 months prior to study initiation; to avoid confounding the vaccine's effects with pre-existing conditions.
- Received a cholera vaccine in the last 24 months: Ensures that the study assesses the vaccine in question without interference from prior vaccinations.
- History of cholera disease in the last 24 months: Recent history of cholera infection can interfere with the measurement of vaccine response.
- Severely malnourished individuals as determined by mid-upper arm circumference (MUAC) and age-specific body mass index (BMI) measurements: malnutrition can affect immune response and vaccine efficacy. In children below 510 years, severe malnutrition will be defined as MUAC < 11.5 cm, for older children (age 5 - 17y) severe malnutrition will be defined as BMI-for-age z score < -3 (WHO Child Growth Standards), for children <10y, presence of bilateral pitting oedema will be considered indicative of severe malnutrition. For adults (18y and above), severe malnutrition will be while in older children and adults it will be defined as BMI < 16.
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- Non-HIV/AIDS immunosuppressive condition or on immunosuppressive therapy: Such conditions can significantly alter vaccine response.
- Presence of bleeding disorders or medical contraindication for blood draws: To ensure participant safety during blood collection.
- Participation in another clinical trial with investigational product dosing within 6 months prior to study initiation.
- An individual thought to have difficulty in participating in the study due to severe chronic diseases, based on the judgment of the investigator.
- An individual thought to have difficulty participating in the study due to reasons, such as significant logistical constraints, or communication barriers, or likely to be away for a period of at least 3 consecutive months in the first 6 months of enrollment based on the judgment of the investigator.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Official title: A Phase IV Parallel-Group, Open-Label, Randomized Non-Inferiority Trial Evaluating Immunogenicity of Extended Dosing Intervals for Euvichol-S Oral Cholera Vaccine, Nairobi, Kenya
Background: Despite efforts to control cholera, outbreaks continue to occur in Kenya. Oral cholera vaccines (OCVs) are a critical tool in cholera prevention strategies. This study evaluates the immunogenicity of extended dosing intervals for Euvichol-S, a WHO-prequalified OCV, in a Phase IV non-inferiority trial.
Overview Design: This trial is a parallel-group, open-label, randomized, non-inferiority study. It aims to compare the immune response of three dosing schedules of the Euvichol-S OCV: a standard 2-week interval, a 2-month interval, and a 12-month interval. The study will enroll 1071 participants, stratified by age into three groups (1-4 years, 5-14 years, 15+ years. The primary endpoint is the plasma vibriocidal geometric mean titer (GMT) measured two weeks after the second dose.
Read more
Primary Objective: To assess and compare the immune response to Euvichol-S measured by vibriocidal GMT two weeks after the second vaccine dose across different dosing intervals.
Study Sites: The study will be conducted in the Mukuru informal settlement in Nairobi, Kenya, a high-priority cholera hotspot area. The Kenya Medical Research Institute (KEMRI) will manage the study, leveraging its established relationship with the community.
Study Population: Inclusion criteria include residents of Mukuru ≥1 year, who are healthy as determined by medical history and physical examination. Exclusion criteria include pregnant women, severe malnutrition, and non-HIV immunosuppressive conditions or severe chronic diseases.
Study Interventions: Participants will be randomized to one of three dosing arms stratified by age: a standard 2-week interval, a 3-month interval, or an annual booster interval. Participants will receive the Euvichol-S OCV according to the assigned schedule. The follow-up period for participants will be 18 months, during which they will undergo regular scheduled visits and additional unscheduled visits as needed (i.e., standard dosing arm: six scheduled visits; 3-month interval arm: 7 visits; annual booster arm: 6 visits). Blood samples will be collected at each vaccination visit and 14 days later and at 6 months, 1 year and 18 months after enrollment to measure plasma vibriocidal GMT and other immunological markers. Older children in the PBMC cohort will have two additional samples collected five days after each vaccine dose and a larger blood volume (10mls) collected at 14 days after the second dose.
Outcome Measures: Primary outcome measures include the plasma vibriocidal GMT two weeks post-second dose. Secondary outcomes include antibody seroconversion rates, longitudinal GMT changes, incidence of cholera disease, and the safety profile of the vaccine. The PBMC sub-cohort will provide detailed insights into memory B cell and plasmablast responses.
Sample Size: The study will enroll 1071 participants with equal distribution across the three dosing arms and age strata. The PBMC sub-cohort will include 240 participants (40 per arm among 5-14 years, 40 per arm 1-4 years), with detailed immunological assessments.
Data Analysis: The immunogenicity of the vaccine across different dosing schedules will be compared to determine non-inferiority. Data will be analyzed descriptively to summarize the by-grade incidence of treatment-emergent adverse events (AEs), serious adverse events (SAEs), and other safety indicators.
Impact: This trial aims to generate evidence on the optimal dosing schedule for Euvichol-S OCV, potentially informing future vaccination strategies in cholera-endemic regions and improving cholera prevention in resource-limited settings.
Read the detailed description
Study Rationale Between October 2022 and February 2024, Kenya has experienced a cholera outbreak with over 10,000 reported cases and 166 deaths across 23 counties. Alarmingly, children under 10 years of age account for one-third of the documented cases, indicating their heightened vulnerability to the disease. In February 2023, Kenya vaccinated more than 2.2 million people with a single dose of oral cholera vaccine (OCV). However, this reactive campaign alone has proven insufficient to control the outbreak.
To address endemic cholera and prevent future outbreaks, the Kenya MoH has applied to Gavi, the Vaccine Alliance, to receive OCV for a preventive vaccination campaign in 2025 to 2028. Based on recent hotspot mapping led by partners in our consortium, the government plans to conduct mass vaccination campaigns in 94 hotspot sub-counties, reaching 19 million individuals. This campaign will mark the first national preventive campaign of OCV in East Africa. Insights gained will benefit not only Kenya but also neighbouring countries experiencing cholera outbreaks.
Studies evaluating the relative impact of campaigns utilizing two doses with extended intervals are limited. Additionally, prior studies assessing extended dosing intervals have not compared durability and immunogenicity within specific age groups, nor have they consistently included extended follow-up periods. Given the specific vulnerability of children, the Global Task Force for Cholera Control ranks research on optimal cholera vaccine schedules for children one to five years as the highest priority in the Cholera Roadmap Research Agenda.
Vaccination with OCV is a proven, effective strategy to prevent cholera outbreaks. However, the current manufacturer-recommended dosing regimen is challenging to implement programmatically and offers only short-term protection, particularly in young children, the most vulnerable population. This study aims to address this gap by generating evidence on the immunogenicity and durability of immunity across different dosing schedules. By evaluating the immune response, particularly in children, this trial will provide critical data to inform optimal dosing strategies. The findings will support the Kenyan Ministry of Health in enhancing the impact of preventive OCV campaigns and improving long-term cholera control efforts in endemic regions.
Risks and Benefits
Known Potential Risks
Associated with oral vaccine administration:
Mild to moderate side effects, such as gastrointestinal discomfort, nausea, or diarrhea, may occur.
Serious allergic reactions, though rare, are a possibility and will be monitored.
Behaviour Change:
Although the literature on preventative behaviors suggest that it is highly unlikely, it is theoretically possible that participants might alter their risk behaviors assuming they are protected post-vaccination. They will be advised to continue following cholera prevention measures.
Specific Risks from Euvichol-S Vaccine:
Euvichol-S is generally well-tolerated. In the phase 3 clinical trial, of 1,595 participants who received the product, 151 (<10%) reported any adverse event. The most common adverse events after vaccination were pyrexia (3.6%) and nasopharyngitis (2.2%).
The specific risks associated with different dosing intervals of Euvichol-S are under study. Participants will be informed of any known risks related to the vaccine.
Community Perceptions:
Participation in the vaccine trial might affect community perceptions towards the participant. Efforts will be made to maintain confidentiality and manage community relations carefully.
Associated with Venous Puncture:
While generally safe, venous puncture can result in discomfort or minor reactions such as pain at the puncture site, bruising, or occasional bleeding. Participants will receive instructions to minimize and manage these potential effects.
Vaccine efficacy risks:
One dose of oral cholera vaccine offers short-term protection against cholera, necessitating a second dose for longer-term immunity. Our hypothesis is that longer intervals between doses (3-months and 1 year) will result in similar long-term immunity at 1 year after the delayed booster dose as with the standard 2-week dosing interval at 1 year after the booster dose; however, it is possible that protection against cholera may diminish prior to the 2nd dose. These risks will be clearly communicated to participants, and any new information regarding vaccine efficacy will be communicated as it becomes available.
Known Potential Benefits Euvichol-S oral cholera vaccine induces a protective immune response against cholera. Thus, participants in this study who receive the vaccine are expected to have a lower risk of cholera compared to those who are not enrolled in the trial and do not receive immunization. Additionally, participants in this trial will receive the vaccine before it becomes widely available through government vaccination campaigns. This early access to the vaccine provides an immediate benefit in reducing their risk of cholera infection. Furthermore, this study aims to enhance the understanding of cholera vaccination strategies, potentially leading to more effective public health interventions against cholera globally.
Assessment of Potential Risks and Benefits
The trial balances the mild to moderate side effects and the rare but serious risks of allergic reactions from the Euvichol-S oral cholera vaccine against the expected benefit of reduced cholera risk among participants. While there are uncertainties regarding the longevity of protection, especially between dosing intervals, the study is critical for optimizing vaccination schedules and enhancing global cholera prevention strategies.
Objectives and Endpoints The primary objective is to assess and compare the immune response, specifically plasma vibriocidal GMT, two weeks post-second dose of Euvichol-S, across three dosing intervals: 2-weeks, 3-months and 1-year. Our secondary objectives expand on this by evaluating seroconversion, immune response within different age groups, monitoring long-term GMT differences, assessing cholera incidence, and documenting the vaccine's safety profile over extended dosing intervals. Additionally, our exploratory objectives include, analyzing V. cholerae O-specific polysaccharide (OSP)-specific plasma antibody, circulating gut-homing plasmablasts (a surrogate marker for the mucosal immune response), and memory B cell response magnitude and dynamics, to gain comprehensive insights into the vaccine's immunogenicity over 18 months.
Primary Objective To assess and compare the immune response to Euvichol-S, measured by plasma vibriocidal geometric mean titer (GMT) two weeks after the second vaccine dose, across different dosing intervals in participants aged 1 year and older.
Hypotheses:
The immune response to a three-month or twelve-month dosing interval of Euvichol-S is non-inferior to the recommended two-week interval in participants aged 1 year and older two weeks after the second dose.
This non-inferiority persists within specific age groups: young children (1-4 years), older children (5-14 years), and adults (15+ years), as measured at 6 months, 12 months, and 18 months after enrollment.
Secondary Objectives To compare plasma vibriocidal GMT across different dosing intervals within specific age groups.
To evaluate vibriocidal antibody seroconversion in relation to dosing intervals among all participants and within each age group.
To monitor and document the changes in vibriocidal GMT over an 18-month follow-up period, comparing between dosing interval groups and within age groups.
To assess and compare the incidence of cholera disease over an 18-month follow-up, focusing on the association with age groups and dosing intervals.
To evaluate and describe the safety and tolerability profile of extended dosing intervals of Euvichol-S.
Exploratory Objectives Assess and compare the following measures a) among all study participants and b) within each age group: Anti-O-specific polysaccharide (OSP) IgA and IgG responses in plasma over an 18-month follow-up period
Circulating gut-homing anti-OSP plasmablasts at baseline and 5 days after each dose of vaccine in a subcohort of children under 15 years Circulating anti-OSP memory B cells at baseline and 14 days after booster doses after each dose of vaccine in a subcohort of children under 15 years Assess and compare the persistence of plasma anti-OSP and vibriocidal immune response over an 18-month follow-up period by age group and dosing interval.
Cholera Disease Incidence Comparison: This involves comparing the incidence of cholera over 18 months across different age groups and dosing intervals. It is a direct measure of the vaccine's effectiveness in preventing the disease in the real-world setting.
Safety Profile Assessment: Investigators will record and analyze adverse events, spanning 18 months from the initial vaccination to the final follow-up, to assess the vaccine's safety over different dosing schedules.
- Conditions
- Cholera Vaccination
- Being tested
- Euvichol-S Oral Cholera Vaccine
- Keywords
- Cholera, extended dosing, Euvichol-S, OCV, vaccination, immunization
- Medical subject headings
- Cholera
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Euvichol-S Oral Cholera VaccineDrug
Also called cholera: inactivated oral, Euvichol
Parallel-group, phase IV, open-label, randomized, non-inferiority trial
Arms:
Three distinct arms, each balanced in a 1:1:1 ratio:
Standard Dosing Arm (Two Weeks Interval) Extended Interval Dosing Arm (Three Months Interval) Annual Booster Dosing Arm (Twelve Months Interval)
Each dosing arm will have the following three age strata:
Children aged 1-4 years Children aged 5-14 years Adults aged 15 years and older
| Study group | Role | What they receive |
|---|---|---|
| Standard Dosing Arm (Two Weeks Interval) | Active comparator | Participants received the second OCV dose per the recommended dosing schedule 2 weeks after the initial dose. Receives: Drug: Euvichol-S Oral Cholera Vaccine |
| Extended Interval Dosing Arm (Three Months Interval) | Experimental | Participants received the second OCV dose 3 months after the initial dose. Receives: Drug: Euvichol-S Oral Cholera Vaccine |
| Annual Booster Dosing Arm (Twelve Months Interval) | Experimental | Participants received the second OCV dose 12 months after the initial dose. Receives: Drug: Euvichol-S Oral Cholera Vaccine |
What is being measured
The primary outcome is the main question the study is designed to answer.
To assess and compare the immune response to Euvichol-S, measured by plasma vibriocidal geometric mean titer (GMT) two weeks after the second vaccine dose, across different dosing intervals in participants aged 1 year and older.
Plasma Vibriocidal GMT Measurement: Measurement of the concentration of plasma vibriocidal GMT two weeks after administering the second dose of Euvichol-S. Vibriocidal antibodies are the best-established immune correlate of protection against cholera. The GMT, a statistical representation of the antibody levels in the study population, is an objective and quantifiable measure of the vaccine's immunogenicity. By comparing GMT values across different dosing intervals, we aim to validate the immunogenicity of extended dosing schedules, assessing if they are as effective at eliciting a protective immune response as the standard two-week interval. This assessment will be crucial in guiding future vaccination strategies, particularly in resource-limited settings where scheduling flexibility can significantly impact public health outcomes.
Measured: Plasma vibriocidal GMT measurement 2-weeks after the 2nd vaccine dose of Euvichol-S in participants 1+ years for the Comparator Arm (2nd dose at 2 weeks), Intervention Arm 1 (2nd dose at 3-months), and Intervention Arm 2 (2nd dose at 1-year)
Secondary outcomes (1)
Plasma Vibriocidal GMT
Plasma Vibriocidal GMT Comparison: Compare the concentration of plasma vibriocidal geometric mean titer (GMT) across various dosing intervals within distinct age groups to determine whether the average antibody levels within each age strata varies by the vaccine dosing schedule.
Vibriocidal Antibody Seroconversion Evaluation: Assess the proportion of vaccinees who had a 4-fold or greater rise in vibriocidal titers after vaccination, indicating the development of an immune response to the vaccine.
Longitudinal GMT Changes Monitoring: Describe plasma vibriocidal GMT over an 18-month period: two weeks post-vaccination and also at 6, 12, and 18 months post-enrollment; this outcome tracks the persistence and variation of GMT by dosing interval and age to understand the duration and stability of the immune response elicited by the vaccine.
Cholera Disease Incidence Comparison: Compare the incidence of cholera over 18 months across different age groups and dosing intervals.
Measured: Plasma vibriocidal GMT over an 18-month period: two weeks post-vaccination and also at 6, 12, and 18 months post-enrollment.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Mar 2026
- Study start31 Oct 2025
- Primary completionJun 2028 (estimated)
- Study completionJun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cholera VaccinationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 4
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Parallel-group, phase IV, open-label, randomized, non-inferiority trial Arms: Three distinct arms, each balanced in a 1:1:1 ratio: Standard Dosing Arm (Two Weeks Interval) Extended Interval Dosing Arm (Three Months Interval) Annual Booster Dosing Arm (Twelve Months Interval) Each dosing arm will have the following three age strata: Children aged 1-4 years Children aged 5-14 years Adults aged 15 years and older
- Masking
- None (open label)
- Enrolment
- 1,071 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Albert B. Sabin Vaccine Institute
- Sponsor type
- University, hospital or other
- Collaborators
- Kenya Medical Research Institute, Washington State University, Massachusetts General Hospital, Kenya Ministry of Health, Nairobi City County
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07487077
- Sponsor's protocol ID
- Sabin-OCV-24
- Other IDs
- Wellcome Grant Number: 228242/
- Status last verified
- Mar 2026
- First submitted
- 4 Mar 2026
- Last updated
- 23 Mar 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase IV Parallel-Group, Open-Label, Randomized Non-Inferiority Trial Evaluating Immunogenicity of Extended Dosing Intervals for Euvichol-S Oral Cholera Vaccine, Nairobi, Kenya
- ClinicalTrials.gov ID
- NCT07487077
- Acronym / sponsor ID
- Sabin-OCV-24
- Conditions
- Cholera Vaccination
- Keywords
- Cholera, extended dosing, Euvichol-S, OCV, vaccination, immunization
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,071 participants (estimated)
- Lead sponsor
- Albert B. Sabin Vaccine InstituteUniversity, hospital or other
- Collaborators
- Kenya Medical Research Institute, Washington State University, Massachusetts General Hospital, Kenya Ministry of Health, Nairobi City County
- Study start
- 31 Oct 2025 (actual)
- Primary completion
- Jun 2028 (estimated)
- Study completion
- Jun 2028 (estimated)
- First posted
- 23 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background: Despite efforts to control cholera, outbreaks continue to occur in Kenya. Oral cholera vaccines (OCVs) are a critical tool in cholera prevention strategies. This study evaluates the immunogenicity of extended dosing intervals for Euvichol-S, a WHO-prequalified OCV, in a Phase IV non-inferiority trial.
Overview Design: This trial is a parallel-group, open-label, randomized, non-inferiority study. It aims to compare the immune response of three dosing schedules of the Euvichol-S OCV: a standard 2-week interval, a 2-month interval, and a 12-month interval. The study will enroll 1071 participants, stratified by age into three groups (1-4 years, 5-14 years, 15+ years. The primary endpoint is the plasma vibriocidal geometric mean titer (GMT) measured two weeks after the second dose.
Primary Objective: To assess and compare the immune response to Euvichol-S measured by vibriocidal GMT two weeks after the second vaccine dose across different dosing intervals.
Study Sites: The study will be conducted in the Mukuru informal settlement in Nairobi, Kenya, a high-priority cholera hotspot area. The Kenya Medical Research Institute (KEMRI) will manage the study, leveraging its established relationship with the community.
Study Population: Inclusion criteria include residents of Mukuru ≥1 year, who are healthy as determined by medical history and physical examination. Exclusion criteria include pregnant women, severe malnutrition, and non-HIV immunosuppressive conditions or severe chronic diseases.
Study Interventions: Participants will be randomized to one of three dosing arms stratified by age: a standard 2-week interval, a 3-month interval, or an annual booster interval. Participants will receive the Euvichol-S OCV according to the assigned schedule. The follow-up period for participants will be 18 months, during which they will undergo regular scheduled visits and additional unscheduled visits as needed (i.e., standard dosing arm: six scheduled visits; 3-month interval arm: 7 visits; annual booster arm: 6 visits). Blood samples will be collected at each vaccination visit and 14 days later and at 6 months, 1 year and 18 months after enrollment to measure plasma vibriocidal GMT and other immunological markers. Older children in the PBMC cohort will have two additional samples collected five days after each vaccine dose and a larger blood volume (10mls) collected at 14 days after the second dose.
Outcome Measures: Primary outcome measures include the plasma vibriocidal GMT two weeks post-second dose. Secondary outcomes include antibody seroconversion rates, longitudinal GMT changes, incidence of cholera disease, and the safety profile of the vaccine. The PBMC sub-cohort will provide detailed insights into memory B cell and plasmablast responses.
Sample Size: The study will enroll 1071 participants with equal distribution across the three dosing arms and age strata. The PBMC sub-cohort will include 240 participants (40 per arm among 5-14 years, 40 per arm 1-4 years), with detailed immunological assessments.
Data Analysis: The immunogenicity of the vaccine across different dosing schedules will be compared to determine non-inferiority. Data will be analyzed descriptively to summarize the by-grade incidence of treatment-emergent adverse events (AEs), serious adverse events (SAEs), and other safety indicators.
Impact: This trial aims to generate evidence on the optimal dosing schedule for Euvichol-S OCV, potentially informing future vaccination strategies in cholera-endemic regions and improving cholera prevention in resource-limited settings.
Detailed description
Study Rationale Between October 2022 and February 2024, Kenya has experienced a cholera outbreak with over 10,000 reported cases and 166 deaths across 23 counties. Alarmingly, children under 10 years of age account for one-third of the documented cases, indicating their heightened vulnerability to the disease. In February 2023, Kenya vaccinated more than 2.2 million people with a single dose of oral cholera vaccine (OCV). However, this reactive campaign alone has proven insufficient to control the outbreak.
To address endemic cholera and prevent future outbreaks, the Kenya MoH has applied to Gavi, the Vaccine Alliance, to receive OCV for a preventive vaccination campaign in 2025 to 2028. Based on recent hotspot mapping led by partners in our consortium, the government plans to conduct mass vaccination campaigns in 94 hotspot sub-counties, reaching 19 million individuals. This campaign will mark the first national preventive campaign of OCV in East Africa. Insights gained will benefit not only Kenya but also neighbouring countries experiencing cholera outbreaks.
Studies evaluating the relative impact of campaigns utilizing two doses with extended intervals are limited. Additionally, prior studies assessing extended dosing intervals have not compared durability and immunogenicity within specific age groups, nor have they consistently included extended follow-up periods. Given the specific vulnerability of children, the Global Task Force for Cholera Control ranks research on optimal cholera vaccine schedules for children one to five years as the highest priority in the Cholera Roadmap Research Agenda.
Vaccination with OCV is a proven, effective strategy to prevent cholera outbreaks. However, the current manufacturer-recommended dosing regimen is challenging to implement programmatically and offers only short-term protection, particularly in young children, the most vulnerable population. This study aims to address this gap by generating evidence on the immunogenicity and durability of immunity across different dosing schedules. By evaluating the immune response, particularly in children, this trial will provide critical data to inform optimal dosing strategies. The findings will support the Kenyan Ministry of Health in enhancing the impact of preventive OCV campaigns and improving long-term cholera control efforts in endemic regions.
Risks and Benefits
Known Potential Risks
Associated with oral vaccine administration:
Mild to moderate side effects, such as gastrointestinal discomfort, nausea, or diarrhea, may occur.
Serious allergic reactions, though rare, are a possibility and will be monitored.
Behaviour Change:
Although the literature on preventative behaviors suggest that it is highly unlikely, it is theoretically possible that participants might alter their risk behaviors assuming they are protected post-vaccination. They will be advised to continue following cholera prevention measures.
Specific Risks from Euvichol-S Vaccine:
Euvichol-S is generally well-tolerated. In the phase 3 clinical trial, of 1,595 participants who received the product, 151 (<10%) reported any adverse event. The most common adverse events after vaccination were pyrexia (3.6%) and nasopharyngitis (2.2%).
The specific risks associated with different dosing intervals of Euvichol-S are under study. Participants will be informed of any known risks related to the vaccine.
Community Perceptions:
Participation in the vaccine trial might affect community perceptions towards the participant. Efforts will be made to maintain confidentiality and manage community relations carefully.
Associated with Venous Puncture:
While generally safe, venous puncture can result in discomfort or minor reactions such as pain at the puncture site, bruising, or occasional bleeding. Participants will receive instructions to minimize and manage these potential effects.
Vaccine efficacy risks:
One dose of oral cholera vaccine offers short-term protection against cholera, necessitating a second dose for longer-term immunity. Our hypothesis is that longer intervals between doses (3-months and 1 year) will result in similar long-term immunity at 1 year after the delayed booster dose as with the standard 2-week dosing interval at 1 year after the booster dose; however, it is possible that protection against cholera may diminish prior to the 2nd dose. These risks will be clearly communicated to participants, and any new information regarding vaccine efficacy will be communicated as it becomes available.
Known Potential Benefits Euvichol-S oral cholera vaccine induces a protective immune response against cholera. Thus, participants in this study who receive the vaccine are expected to have a lower risk of cholera compared to those who are not enrolled in the trial and do not receive immunization. Additionally, participants in this trial will receive the vaccine before it becomes widely available through government vaccination campaigns. This early access to the vaccine provides an immediate benefit in reducing their risk of cholera infection. Furthermore, this study aims to enhance the understanding of cholera vaccination strategies, potentially leading to more effective public health interventions against cholera globally.
Assessment of Potential Risks and Benefits
The trial balances the mild to moderate side effects and the rare but serious risks of allergic reactions from the Euvichol-S oral cholera vaccine against the expected benefit of reduced cholera risk among participants. While there are uncertainties regarding the longevity of protection, especially between dosing intervals, the study is critical for optimizing vaccination schedules and enhancing global cholera prevention strategies.
Objectives and Endpoints The primary objective is to assess and compare the immune response, specifically plasma vibriocidal GMT, two weeks post-second dose of Euvichol-S, across three dosing intervals: 2-weeks, 3-months and 1-year. Our secondary objectives expand on this by evaluating seroconversion, immune response within different age groups, monitoring long-term GMT differences, assessing cholera incidence, and documenting the vaccine's safety profile over extended dosing intervals. Additionally, our exploratory objectives include, analyzing V. cholerae O-specific polysaccharide (OSP)-specific plasma antibody, circulating gut-homing plasmablasts (a surrogate marker for the mucosal immune response), and memory B cell response magnitude and dynamics, to gain comprehensive insights into the vaccine's immunogenicity over 18 months.
Primary Objective To assess and compare the immune response to Euvichol-S, measured by plasma vibriocidal geometric mean titer (GMT) two weeks after the second vaccine dose, across different dosing intervals in participants aged 1 year and older.
Hypotheses:
The immune response to a three-month or twelve-month dosing interval of Euvichol-S is non-inferior to the recommended two-week interval in participants aged 1 year and older two weeks after the second dose.
This non-inferiority persists within specific age groups: young children (1-4 years), older children (5-14 years), and adults (15+ years), as measured at 6 months, 12 months, and 18 months after enrollment.
Secondary Objectives To compare plasma vibriocidal GMT across different dosing intervals within specific age groups.
To evaluate vibriocidal antibody seroconversion in relation to dosing intervals among all participants and within each age group.
To monitor and document the changes in vibriocidal GMT over an 18-month follow-up period, comparing between dosing interval groups and within age groups.
To assess and compare the incidence of cholera disease over an 18-month follow-up, focusing on the association with age groups and dosing intervals.
To evaluate and describe the safety and tolerability profile of extended dosing intervals of Euvichol-S.
Exploratory Objectives Assess and compare the following measures a) among all study participants and b) within each age group: Anti-O-specific polysaccharide (OSP) IgA and IgG responses in plasma over an 18-month follow-up period
Circulating gut-homing anti-OSP plasmablasts at baseline and 5 days after each dose of vaccine in a subcohort of children under 15 years Circulating anti-OSP memory B cells at baseline and 14 days after booster doses after each dose of vaccine in a subcohort of children under 15 years Assess and compare the persistence of plasma anti-OSP and vibriocidal immune response over an 18-month follow-up period by age group and dosing interval.
Cholera Disease Incidence Comparison: This involves comparing the incidence of cholera over 18 months across different age groups and dosing intervals. It is a direct measure of the vaccine's effectiveness in preventing the disease in the real-world setting.
Safety Profile Assessment: Investigators will record and analyze adverse events, spanning 18 months from the initial vaccination to the final follow-up, to assess the vaccine's safety over different dosing schedules.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Parallel-group, phase IV, open-label, randomized, non-inferiority trial Arms: Three distinct arms, each balanced in a 1:1:1 ratio: Standard Dosing Arm (Two Weeks Interval) Extended Interval Dosing Arm (Three Months Interval) Annual Booster Dosing Arm (Twelve Months Interval) Each dosing arm will have the following three age strata: Children aged 1-4 years Children aged 5-14 years Adults aged 15 years and older
| Arm | Type | Receives |
|---|---|---|
| Standard Dosing Arm (Two Weeks Interval) | Active comparator | Drug: Euvichol-S Oral Cholera VaccineParticipants received the second OCV dose per the recommended dosing schedule 2 weeks after the initial dose. |
| Extended Interval Dosing Arm (Three Months Interval) | Experimental | Drug: Euvichol-S Oral Cholera VaccineParticipants received the second OCV dose 3 months after the initial dose. |
| Annual Booster Dosing Arm (Twelve Months Interval) | Experimental | Drug: Euvichol-S Oral Cholera VaccineParticipants received the second OCV dose 12 months after the initial dose. |
Who may qualify
- Ages
- 1 year and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (6 listed)
- Residents of Mukuru, Nairobi, Kenya
- Individuals aged 1 year and above
- Voluntary written informed consent for study participation provided by an individual or his/her legally acceptable representative. Children aged 13 years and above will also provide assent, with parental permission required for all children.
- Ability to comply with study requirements and attend follow-up visits during the study period.
- Participants must be in good health, as determined by medical history, physical examination, and the clinical judgment of the investigators. Clinical judgment will consider factors such as the absence of acute illness or, uncontrolled or severe chronic conditions that may affect participation in the study.
Key exclusion criteria (11 listed)
- Known history of hypersensitivity reactions to other vaccines.
- Pregnant women, due to differences in immune response. A pregnancy test will be administered to all female participants who have reached menarche and are under 50 years.
- Reported diarrhea or abdominal pain lasting 2 weeks or longer within 6 months prior to study initiation; to avoid confounding the vaccine's effects with pre-existing conditions.
- Received a cholera vaccine in the last 24 months: Ensures that the study assesses the vaccine in question without interference from prior vaccinations.
- History of cholera disease in the last 24 months: Recent history of cholera infection can interfere with the measurement of vaccine response.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Euvichol-S Oral Cholera VaccineAlso: cholera: inactivated oral, EuvicholParallel-group, phase IV, open-label, randomized, non-inferiority trial Arms: Three distinct arms, each balanced in a 1:1:1 ratio: Standard Dosing Arm (Two Weeks Interval) Extended Interval Dosing Arm (Three Months Interval) Annual Booster Dosing Arm (Twelve Months Interval) Each dosing arm will have the following three age strata: Children aged 1-4 years Children aged 5-14 years Adults aged 15 years and older | Drug | Annual Booster Dosing Arm (Twelve Months Interval), Extended Interval Dosing Arm (Three Months Interval), Standard Dosing Arm (Two Weeks Interval) |
Primary outcome
To assess and compare the immune response to Euvichol-S, measured by plasma vibriocidal geometric mean titer (GMT) two weeks after the second vaccine dose, across different dosing intervals in participants aged 1 year and older.
Time frame: Plasma vibriocidal GMT measurement 2-weeks after the 2nd vaccine dose of Euvichol-S in participants 1+ years for the Comparator Arm (2nd dose at 2 weeks), Intervention Arm 1 (2nd dose at 3-months), and Intervention Arm 2 (2nd dose at 1-year)
Plasma Vibriocidal GMT Measurement: Measurement of the concentration of plasma vibriocidal GMT two weeks after administering the second dose of Euvichol-S. Vibriocidal antibodies are the best-established immune correlate of protection against cholera. The GMT, a statistical representation of the antibody levels in the study population, is an objective and quantifiable measure of the vaccine's immunogenicity. By comparing GMT values across different dosing intervals, we aim to validate the immunogenicity of extended dosing schedules, assessing if they are as effective at eliciting a protective immune response as the standard two-week interval. This assessment will be crucial in guiding future vaccination strategies, particularly in resource-limited settings where scheduling flexibility can significantly impact public health outcomes.
1 secondary outcome
Plasma Vibriocidal GMT
Time frame: Plasma vibriocidal GMT over an 18-month period: two weeks post-vaccination and also at 6, 12, and 18 months post-enrollment.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Mar 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Euvichol-S Oral Cholera Vaccine in people with Cholera Vaccination, run by Albert B. Sabin Vaccine Institute at 1 site in Kenya.
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 6 inclusion and 11 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: looking for participants now, as of the sponsor's last update on 23 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Kenya. 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. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Samuel Kariuki, BVM, PhD (+254 722232467, samkariuki2@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To assess and compare the immune response to Euvichol-S, measured by plasma vibriocidal geometric mean titer (GMT) two weeks after the second vaccine dose, across different dosing intervals in participants aged 1 year and older. (time frame: Plasma vibriocidal GMT measurement 2-weeks after the 2nd vaccine dose of Euvichol-S in participants 1+ years for the Comparator Arm (2nd dose at 2 weeks), Intervention Arm 1 (2nd dose at 3-months), and Intervention Arm 2 (2nd dose at 1-year)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 23 Mar 2026.