Rotavirus GastroenteritisPhase 3NCT05958771
The Efficacy of Three Doses of Live Attenuated, Oral Rotavirus Vaccine 116E
A Phase 3 study testing ROTAVAC 5D in people with Rotavirus Gastroenteritis, run by University of Chile at 16 sites in Chile.
Trial summary
This is a randomized, double-blind, phase 3 study to evaluate the Efficacy, Safety, and Immunogenicity of ROTAVAC 5D, a live attenuated rotavirus vaccine in healthy infants. A total of 5800 healthy Chilean infants will be recruited in this study and randomized to receive either vaccine or placebo in 1:1 ratio. Read more about this study
- Who is it for?
- Ages 60 to 89 daysHealthy volunteers can take part
- Conditions the study is for
- Rotavirus Gastroenteritis
- What is being tested?
- ROTAVAC 5D
- Type of treatment
- Vaccines, Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 4,270 participants
- Where
- 16 sitesChile
- Study dates
- 6 Jul 2023to 27 Feb 2026
- Phase
- Phase 3
- Are there results?
- None posted in the registry
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 60 to 89 days
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- At least one parent(s) or legally acceptable representative's consent for participation and are able to understand study procedures
- Subjects aged at least 2 months at recruitment
- No plans to move in the next 12 months
Who cannot join
- Administration of rotavirus vaccine in the past
- Participants vaccinated with a dose of vaccine from the National Immunization Program corresponding to their current age, in which more than 48 hours have passed since the last dose received
- Presence of any illness requiring hospital referral (temporary exclusion)
- Known case of immunodeficiency disease, known HIV positive
- Known case of chronic gastroenteritis disease, chronic pulmonary disease, chronic renal disease, congenital heart disease (Stable with no on-going medication).
- Any other conditions which in the judgment of the investigator warrant exclusion (e.g. no exclusion criteria but seems 'ill', investigators suspects neglect)
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- Diarrhea on the day of enrollment (temporary exclusion)
- A known sensitivity or allergy to any components of the study vaccines.
- Major congenital or genetic defect.
- Has received any immunoglobulin therapy and/or blood products since birth.
- History of chronic administration (defined as more than 14 days) of immunosuppressants including corticosteroids. Infants on inhaled or topical steroids may be permitted to participate in the study, at the discretion of the principal investigator.
Trial locations and contacts
16 sites in 1 country.
16 sites in 1 country
Chile16 sites
Vacunatorio Mediped
Antofagasta, Antofagasta, 124 3817
Vacunatorio Kinewen, Concepción
Concepción, Biobio
CESFAM Dr. Alejandro Gutierrez, Coyahique
Coyhaique, Aysén
Hospital Base de Osorno
Osorno, Los Lagos Region
Hospital de Puerto Montt
Port Montt, Los Lagos Region
CESFAM Puerto Aysen
Puerto Aisén, Aysén
CESFAM Colina
Santiago, Metropolitan Region
CESFAM Dr. Alejandro del Rio, Puente Alto
Santiago, Metropolitan Region
CESFAM Esmeralda
Santiago, Metropolitan Region
CESFAM Lo Barnechea
Santiago, Metropolitan Region
Clínica Dávila
Santiago, Metropolitan Region
Hospital de Carabineros
Santiago, Metropolitan Region
Hospital Dr. Exequiel González Cortés
Santiago, Metropolitan Region
Hospital Roberto del Rio
Santiago, Metropolitan Region
CESFAM Jean y Marie Thierry de Valparaíso
Valparaíso, Valparaiso
Hospital Dr. Gustavo Fricke
Viña del Mar
About this study
Official title: The Efficacy of Three Doses of Live Attenuated, Oral Rotavirus Vaccine 116E (ROTAVAC 5D) in Chilean Infants.
This is a randomized, double-blind, phase 3 study to evaluate the Efficacy, Safety, and Immunogenicity of ROTAVAC 5D, a live attenuated rotavirus vaccine in healthy infants.
A total of 5800 healthy Chilean infants will be recruited in this study and randomized to receive either vaccine or placebo in 1:1 ratio. Among these participants 300 will be categorized to immunogenicity cohort, 150 from each group, and blood samples will be collected to assess the immune response.
Read the detailed description
Prior to study initiation, study clinics and offices will be set up in each of the enrollment sites. Awareness about the study will be created in the community. All categories of staff will be recruited and trained. CRFs, SOPs and registers will be developed. Regulatory and IRB approvals will be obtained. Permissions and clearances will be sought from the Government.
The study team will identify pregnant women, newborns and infants aged less than 8 weeks as potential participants. Information about the study will be shared with these families, and those willing to participate will be enrolled after obtaining consent and subsequent screening of the subject. Subjects will be enrolled in the study since 2 months + 29 days of age and will be given 3 doses of the Test Article/placebo along with childhood vaccines (which will include vaccines against diphtheria, pertussis, tetanus, Haemophilus influenzae B, Hepatitis B and IPV, and pneumococcal conjugated vaccine at 2 and 4 month of age). Participants vaccinated with a dose of vaccine from the National Immunization Program corresponding to their current age, in which more than 48 hours have passed since the last dose received, the subject will not be considered for the study. The Test Article will be liquid ORV 116E, 105.0ffu stored at 2-8°C. The Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age. After each visit, a safety evaluation will be carried out on all participants. A card will be given to the caregivers for the daily record of temperature, diarrhea, vomiting, food refusal and/or irritability, for a period of 1 week. On day 3 and 7, the research team will contact the caregivers by telephone to note the general state of health of the infant and to collect the card. The subjects will be followed f or episodes of acute gastroenteritis every two weeks through contact by email or text message (+ 2 days), until 8 months + up to 14 days post 3 doses of vaccination. The expected duration of subjec participation is 13 months. In addition to the contacts at every two weeks follow-up, parents/primary caregiver will be advised to contact the study team whenever the subject has symptoms of gastroenteritis (GE; the operational definition of GE for this study will be the change in the habitual pattern of the stools, both in more frequent passage than is normal for the individual and/or in the decrease in stool consistency), signs or symptoms of suspected intussusception (IS, defined as stomach pain and vomiting that start suddenly and come and go several times per hour, and then later, bloody stools) or any other illness requiring hospital referral. If the caregiver report symptoms of GE, an "illness visit" will be activated. The caregiver will be asked to collect a stool specimen. The field worker will ensure that the parents/primary caregiver have stool containers available with them so that stool specimens can be collected whenever the enrolled subject has GE. In the next 24-48 hours, the stool sample will be processed with an ELISA rotavirus test. If the result is negative, the illness visit will be discontinued, and the episode will be registered. If the result is positive, a daily telephone follow-up will be carried out throughout the GE episode, up to 24 hours after the last altered stool. If during the illness visit any symptom/sign of dehydration and/or clinical severity is verified by the research team, the participant will be invited to be evaluated at the study center. During the illness visit the following variables will be collected daily by the caregiver in an illness visit card: stools number and consistency, vomiting episodes, temperature (based on subjective perception of the caregiver of potential fever, or at the same time point during the consecutive days, preferably between 2 and 8 PM), administration of ORS yes/no, number of administrations, and if possible, volume administered). If the child is hospitalized, the following information will be obtained from hospitalization charts: number and consistency of stool episodes, number of vomiting episodes, highest daily temperature, hydration evaluation, use of ORS and/or IV solutions (volume used and fluid description) duration of hospitalization, and any potential complication. If in the follow-up every two weeks of the participants, an episode that did not activate the illness visit of GE is reported or detected, the episode will be recorded and an attemp t will be made to collect as much data as possible retrospectively.
The study team will contact the parents/primary caregiver through mobile phone and collect the information of the illness visit card.
Out of the enrolled subjects, 150 from each group will constitute the "Immunogenicity Subset".
Visit 1 Baseline (vaccine at 2 Months of age + 29 days):
- The participant will be screened for eligibility based on vitals (heart rate and body temperature) and physical examination.
- If the participant is eligible (in good general health or stable preexisting disease as per the discretion of the Principal investigator).
- A study vaccine/placebo will be administered. Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any immediate adverse event.
- Daily card will be given to the parent/primary caregiver.
- Blood sample (3 mL) will be collected for immunogenicity analysis in a subset of (n=300) participants prior to vaccination.
Visit 2 (vaccine at 4 Months of age, +29 days):
- Study participants will return to the OPD for vitals and physical examination (general and systemic examination). A study vaccine /placebo will be administered.
- Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any adverse event.
- Daily card will be collected and a new card will be given to the parent/primary caregiver.
Visit 3 (vaccine at approximately 6 Months of age, +29 days):
- Study participants will return to the OPD for vitals and physical examination (general and systemic examination). A study vaccine /placebo will be administered.
- Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any adverse event.
- Diary card will be collected and a new card will be given to the parent/primary caregiver. Visit 4 (1 Month after visit 3 ++5days): (only for immunogenicity group)
- Study participants (Subset) will return to the OPD for physical examination (general and systemic examination) and diary card will be collected.
- Blood sample (3 mL) will be collected for immunogenicity analysis in a subset of n=300.
- Diary card (Photograph) will be collected from the non-immunogenic participants. Blood samples: In the "Immunogenicity Subset", 3 ml blood specimens will be collected at baseline and 28 (+) 5 days after the third dose of the Test Article/placebo to assess the anti-rotavirus IgA antibody titer. Stool Specimens: The study team will attempt to collect a stool specimen for every GE episode, preferably within the first 2 days after episode onset . The stool specimen may be collected up to 7 days after the last day of diarrhea. The stool specimens will be sent to the laboratory. If the episode is a suspected intussusception or vaccine associated gastroenteritis that has occurred within four weeks after each dose of the Test Article/placebo, the specimen will be sent to the laboratory immediately for rotavirus testing and typing. For all ELISA RV positive samples, an aliquot of the stool specimen will be assessed for 22 enteropathogens by multiplex-PCR panel and to identify the genotype of the virus.
- Conditions
- Rotavirus Gastroenteritis
- Being tested
- ROTAVAC 5D, Placebo
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ROTAVAC 5DDrug
monovalent vaccine containing suspension of live attenuated rotavirus 116E prepared in Vero cells. Each dose contains NLT 10 e 5.0 FFU
PlaceboDrug
Placebo contains all the excipients of ROTAVAC 5D but without the suspension of live attenuated rotavirus
| Study group | Role | What they receive |
|---|---|---|
| Children who receive the IP | Active comparator | The Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age.
Test article: ROTAVAC 5D, 3 doses. Each dose of 0.5 mL. Administered orally. Receives: Drug: ROTAVAC 5D |
| Children who receive placebo | Placebo comparator | The Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age.
Placebo: 3 doses. Each dose of 0.5 mL. Administered orally. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of subject who suffer a severe rotavirus gastroenteritis according to the Vesikari Score in vaccine arm as compared to placebo
Efficacy of ORV 116E in comparison to a placebo against severe rotavirus gastroenteritis defined as: episode of diarrhea (the passage of three or more loose or watery stools within a 24-hour period), with or without vomiting, with Vesikari score ≥11
Measured: till 8 months +14 days after administering the third dose
Secondary outcomes (12)
Percentage of subject who suffer a moderate-to-severe rotavirus gastroenteritis according to WHO rehydration plan in vaccine arm as compared to placebo
Efficacy of ORV 116E in comparison to a placebo against moderate-to-severe rotavirus gastroenteritis defined as: episode of diarrhea (the passage of three or more loose or watery stools within a 24-hour period), with or without vomiting, that requires overnight hospitalization or rehydration therapy equivalent to World Health Organization (WHO) plan B (oral rehydration therapy) or plan C (intravenous rehydration therapy) in a medical facility such as a hospital, clinic, or supervised rural health care center
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer any severity of rotavirus gastroenteritis according to the Vesikari score in vaccine arm as compared to placebo arm
Any severity of gastroenteritis caused by non vaccine rotavirus
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer moderate-severe rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Efficacy of ORV 116E in comparison to a placebo against rotavirus gastroenteritis defined as: episode of diarrhea (the passage of three or more loose or watery stools within a 24-hour period), with or without vomiting. Moderate-severe will be defined by the requirement of overnight hospitalization or rehydration therapy equivalent to World Health Organization (WHO) plan B (oral rehydration therapy) or plan C (intravenous rehydration therapy) in a medical facility such as a hospital, clinic, or supervised rural health care center.
Rotavirus-only gastroenteritis will be defined as absence of co-pathogens according to Filmarray ® Gastrointestinal Panel.
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer severe (according to Vesikari score) rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Efficacy of ORV 116E in comparison to a placebo against severe (>11 on the 20 point Vesikari scoring scale) rotavirus-only gastroenteritis (absence of co-pathogens according to Filmarray ® Gastrointestinal Panel )Rotavirus-only gastroenteritis will be defined as absence of co-pathogens according to Filmarray ® Gastrointestinal Panel.
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer any severity (according to Vesikari score) of rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Efficacy of ORV 116E in comparison to a placebo against any severity (any score on the 20 point Vesikari scoring scale) of rotavirus only gastroenteritis (absence of co-pathogens
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer severe (>11 on the 20 point Vesikari scoring scale) gastroenteritis irrespective of etiology in vaccine arm as compared to placebo arm
Efficacy of ORV 116E in comparison to a placebo against Severe (>11 on the 20 point Vesikari scoring scale) gastroenteritis irrespective of etiology
Measured: till 8 months +14 days after administering the third dose
Intent to treat efficacy of ROTAVAC 5D against severe rotavirus gastroenteritis
Severe rotavirus gastroenteritis (≥11 on the 20 point Vesikari scoring scale) caused by non-vaccine rotavirus in the intent-to-treat population till 8 months
+14 days after administering the third dose
Measured: till 8 months +14 days after administering the third dose
Percentage of subject who suffer solicited immediate adverse events after each dose in vaccine arm as compared to placebo arm
Safety of ROTAVAC 5D solicited adverse events till 30 minutes after each vaccination (immediate solicited adverse events)
Measured: 0 to 30 minutes after each vaccination.
Percentage of subject who suffer solicited adverse events till 7 days after each dose in vaccine arm as compared to placebo arm
Solicited adverse events occurring within 7 days after each vaccination
Measured: 30 minutes to 7 days after each vaccination.
Percentage of subject who suffer any adverse event in the 4-week period following each dose in vaccine arm as compared to placebo arm
Unsolicited adverse events assessed from day 0 to end of the study in comparison to a placebo will be assessed in a subset of subjects Unsolicited adverse events from day 0 to 28 following each dose in comparison to a placebo will be assessed in a subset of subjects
Measured: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
Percentage of subject who suffer any severe adverse event during the study period in vaccine arm as compared to placebo arm
Any severe adverse event will be assessed in all subjects throughout the study period.
Measured: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
b. Percentage of subject who suffer intussusception during the study period in vaccine arm as compared to placebo arm
Intussusception will be assessed in all subjects throughout the study period.
Measured: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jul 2023
- Study start6 Jul 2023
- Primary completion27 Feb 2026
- Study completion27 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rotavirus GastroenteritisStudies 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 3
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 4,270 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Chile
- Sponsor type
- University, hospital or other
- Collaborators
- Bharat Biotech International Limited
- Responsible party
- Principal investigator, Miguel O'Ryan Gallardo, University of Chile
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05958771
- Sponsor's protocol ID
- BBIL/Rotavac 5D-CHILE /2022
- Status last verified
- Jun 2026
- First submitted
- 23 Jun 2023
- Last updated
- 30 Jun 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 30 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Efficacy of Three Doses of Live Attenuated, Oral Rotavirus Vaccine 116E (ROTAVAC 5D) in Chilean Infants.
- ClinicalTrials.gov ID
- NCT05958771
- Acronym / sponsor ID
- BBIL/Rotavac 5D-CHILE /2022
- Conditions
- Rotavirus Gastroenteritis
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 4,270 participants (actual)
- Lead sponsor
- University of ChileUniversity, hospital or other
- Collaborators
- Bharat Biotech International Limited
- Study start
- 6 Jul 2023 (actual)
- Primary completion
- 27 Feb 2026 (actual)
- Study completion
- 27 Feb 2026 (actual)
- First posted
- 25 Jul 2023 (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.
This is a randomized, double-blind, phase 3 study to evaluate the Efficacy, Safety, and Immunogenicity of ROTAVAC 5D, a live attenuated rotavirus vaccine in healthy infants.
A total of 5800 healthy Chilean infants will be recruited in this study and randomized to receive either vaccine or placebo in 1:1 ratio. Among these participants 300 will be categorized to immunogenicity cohort, 150 from each group, and blood samples will be collected to assess the immune response.
Detailed description
Prior to study initiation, study clinics and offices will be set up in each of the enrollment sites. Awareness about the study will be created in the community. All categories of staff will be recruited and trained. CRFs, SOPs and registers will be developed. Regulatory and IRB approvals will be obtained. Permissions and clearances will be sought from the Government.
The study team will identify pregnant women, newborns and infants aged less than 8 weeks as potential participants. Information about the study will be shared with these families, and those willing to participate will be enrolled after obtaining consent and subsequent screening of the subject. Subjects will be enrolled in the study since 2 months + 29 days of age and will be given 3 doses of the Test Article/placebo along with childhood vaccines (which will include vaccines against diphtheria, pertussis, tetanus, Haemophilus influenzae B, Hepatitis B and IPV, and pneumococcal conjugated vaccine at 2 and 4 month of age). Participants vaccinated with a dose of vaccine from the National Immunization Program corresponding to their current age, in which more than 48 hours have passed since the last dose received, the subject will not be considered for the study. The Test Article will be liquid ORV 116E, 105.0ffu stored at 2-8°C. The Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age. After each visit, a safety evaluation will be carried out on all participants. A card will be given to the caregivers for the daily record of temperature, diarrhea, vomiting, food refusal and/or irritability, for a period of 1 week. On day 3 and 7, the research team will contact the caregivers by telephone to note the general state of health of the infant and to collect the card. The subjects will be followed f or episodes of acute gastroenteritis every two weeks through contact by email or text message (+ 2 days), until 8 months + up to 14 days post 3 doses of vaccination. The expected duration of subjec participation is 13 months. In addition to the contacts at every two weeks follow-up, parents/primary caregiver will be advised to contact the study team whenever the subject has symptoms of gastroenteritis (GE; the operational definition of GE for this study will be the change in the habitual pattern of the stools, both in more frequent passage than is normal for the individual and/or in the decrease in stool consistency), signs or symptoms of suspected intussusception (IS, defined as stomach pain and vomiting that start suddenly and come and go several times per hour, and then later, bloody stools) or any other illness requiring hospital referral. If the caregiver report symptoms of GE, an "illness visit" will be activated. The caregiver will be asked to collect a stool specimen. The field worker will ensure that the parents/primary caregiver have stool containers available with them so that stool specimens can be collected whenever the enrolled subject has GE. In the next 24-48 hours, the stool sample will be processed with an ELISA rotavirus test. If the result is negative, the illness visit will be discontinued, and the episode will be registered. If the result is positive, a daily telephone follow-up will be carried out throughout the GE episode, up to 24 hours after the last altered stool. If during the illness visit any symptom/sign of dehydration and/or clinical severity is verified by the research team, the participant will be invited to be evaluated at the study center. During the illness visit the following variables will be collected daily by the caregiver in an illness visit card: stools number and consistency, vomiting episodes, temperature (based on subjective perception of the caregiver of potential fever, or at the same time point during the consecutive days, preferably between 2 and 8 PM), administration of ORS yes/no, number of administrations, and if possible, volume administered). If the child is hospitalized, the following information will be obtained from hospitalization charts: number and consistency of stool episodes, number of vomiting episodes, highest daily temperature, hydration evaluation, use of ORS and/or IV solutions (volume used and fluid description) duration of hospitalization, and any potential complication. If in the follow-up every two weeks of the participants, an episode that did not activate the illness visit of GE is reported or detected, the episode will be recorded and an attemp t will be made to collect as much data as possible retrospectively.
The study team will contact the parents/primary caregiver through mobile phone and collect the information of the illness visit card.
Out of the enrolled subjects, 150 from each group will constitute the "Immunogenicity Subset".
Visit 1 Baseline (vaccine at 2 Months of age + 29 days):
- The participant will be screened for eligibility based on vitals (heart rate and body temperature) and physical examination.
- If the participant is eligible (in good general health or stable preexisting disease as per the discretion of the Principal investigator).
- A study vaccine/placebo will be administered. Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any immediate adverse event.
- Daily card will be given to the parent/primary caregiver.
- Blood sample (3 mL) will be collected for immunogenicity analysis in a subset of (n=300) participants prior to vaccination.
Visit 2 (vaccine at 4 Months of age, +29 days):
- Study participants will return to the OPD for vitals and physical examination (general and systemic examination). A study vaccine /placebo will be administered.
- Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any adverse event.
- Daily card will be collected and a new card will be given to the parent/primary caregiver.
Visit 3 (vaccine at approximately 6 Months of age, +29 days):
- Study participants will return to the OPD for vitals and physical examination (general and systemic examination). A study vaccine /placebo will be administered.
- Following vaccination, participants will remain at the study site for at least 30minutes of observation to record any adverse event.
- Diary card will be collected and a new card will be given to the parent/primary caregiver. Visit 4 (1 Month after visit 3 ++5days): (only for immunogenicity group)
- Study participants (Subset) will return to the OPD for physical examination (general and systemic examination) and diary card will be collected.
- Blood sample (3 mL) will be collected for immunogenicity analysis in a subset of n=300.
- Diary card (Photograph) will be collected from the non-immunogenic participants. Blood samples: In the "Immunogenicity Subset", 3 ml blood specimens will be collected at baseline and 28 (+) 5 days after the third dose of the Test Article/placebo to assess the anti-rotavirus IgA antibody titer. Stool Specimens: The study team will attempt to collect a stool specimen for every GE episode, preferably within the first 2 days after episode onset . The stool specimen may be collected up to 7 days after the last day of diarrhea. The stool specimens will be sent to the laboratory. If the episode is a suspected intussusception or vaccine associated gastroenteritis that has occurred within four weeks after each dose of the Test Article/placebo, the specimen will be sent to the laboratory immediately for rotavirus testing and typing. For all ELISA RV positive samples, an aliquot of the stool specimen will be assessed for 22 enteropathogens by multiplex-PCR panel and to identify the genotype of the virus.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Children who receive the IP | Active comparator | Drug: ROTAVAC 5DThe Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age. Test article: ROTAVAC 5D, 3 doses. Each dose of 0.5 mL. Administered orally. |
| Children who receive placebo | Placebo comparator | Drug: PlaceboThe Test Article/placebo will be co-administered with the childhood vaccines that are scheduled at the regular National Program of Immunization vaccination visits around 2 months, 4 months and 6 months of age. Placebo: 3 doses. Each dose of 0.5 mL. Administered orally. |
Who may qualify
- Ages
- 60 to 89 days
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (3 listed)
- At least one parent(s) or legally acceptable representative's consent for participation and are able to understand study procedures
- Subjects aged at least 2 months at recruitment
- No plans to move in the next 12 months
Key exclusion criteria (11 listed)
- Administration of rotavirus vaccine in the past
- Participants vaccinated with a dose of vaccine from the National Immunization Program corresponding to their current age, in which more than 48 hours have passed since the last dose received
- Presence of any illness requiring hospital referral (temporary exclusion)
- Known case of immunodeficiency disease, known HIV positive
- Known case of chronic gastroenteritis disease, chronic pulmonary disease, chronic renal disease, congenital heart disease (Stable with no on-going medication).
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 |
|---|---|---|
| ROTAVAC 5Dmonovalent vaccine containing suspension of live attenuated rotavirus 116E prepared in Vero cells. Each dose contains NLT 10 e 5.0 FFU | Drug | Children who receive the IP |
| PlaceboPlacebo contains all the excipients of ROTAVAC 5D but without the suspension of live attenuated rotavirus | Drug | Children who receive placebo |
Primary outcome
Percentage of subject who suffer a severe rotavirus gastroenteritis according to the Vesikari Score in vaccine arm as compared to placebo
Time frame: till 8 months +14 days after administering the third dose
Efficacy of ORV 116E in comparison to a placebo against severe rotavirus gastroenteritis defined as: episode of diarrhea (the passage of three or more loose or watery stools within a 24-hour period), with or without vomiting, with Vesikari score ≥11
12 secondary outcomes
Percentage of subject who suffer a moderate-to-severe rotavirus gastroenteritis according to WHO rehydration plan in vaccine arm as compared to placebo
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer any severity of rotavirus gastroenteritis according to the Vesikari score in vaccine arm as compared to placebo arm
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer moderate-severe rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer severe (according to Vesikari score) rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer any severity (according to Vesikari score) of rotavirus-only gastroenteritis (absence of co-pathogens) in vaccine arm as compared to placebo arm
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer severe (>11 on the 20 point Vesikari scoring scale) gastroenteritis irrespective of etiology in vaccine arm as compared to placebo arm
Time frame: till 8 months +14 days after administering the third dose
Intent to treat efficacy of ROTAVAC 5D against severe rotavirus gastroenteritis
Time frame: till 8 months +14 days after administering the third dose
Percentage of subject who suffer solicited immediate adverse events after each dose in vaccine arm as compared to placebo arm
Time frame: 0 to 30 minutes after each vaccination.
Percentage of subject who suffer solicited adverse events till 7 days after each dose in vaccine arm as compared to placebo arm
Time frame: 30 minutes to 7 days after each vaccination.
Percentage of subject who suffer any adverse event in the 4-week period following each dose in vaccine arm as compared to placebo arm
Time frame: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
Percentage of subject who suffer any severe adverse event during the study period in vaccine arm as compared to placebo arm
Time frame: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
b. Percentage of subject who suffer intussusception during the study period in vaccine arm as compared to placebo arm
Time frame: from day 0 to end of the study ( till 1 year (12 months) + up to 14 days)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jun 2026.
- Individual participant dataSharing planned: Undecided
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
16 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing ROTAVAC 5D in people with Rotavirus Gastroenteritis, run by University of Chile at 16 sites in Chile.
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 3 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: finished, as of the sponsor's last update on 30 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 16 sites in Chile. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Percentage of subject who suffer a severe rotavirus gastroenteritis according to the Vesikari Score in vaccine arm as compared to placebo (time frame: till 8 months +14 days after administering the third dose). 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 30 Jun 2026.