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New polio vaccine shows promise in large infant trial

NCT ID NCT07297186

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This completed Phase 3 trial tested a new Sabin strain inactivated polio vaccine (sIPV) in 1200 healthy infants aged 2 months. The study compared the new vaccine to a standard polio vaccine to see if it was safe and triggered a strong immune response. The goal is to offer a more affordable and safer option to help eliminate polio worldwide.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Sabin strain inactivated poliovirus vaccine (sIPV)
What this could lead to
If successful, this could provide a safer and more affordable polio vaccine option for infants, helping global eradication efforts.
What could go wrong
This is a completed Phase 3 trial, but results are not yet published. The vaccine may not be as effective as the current standard, or could have unexpected side effects.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

1,200 people

The number who actually took part.

Started

Aug 2017

Finished

Apr 2023

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

60 to 89 days

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Healthy permanent residents aged 2 months (60\~89 days); 2. Infant's legal guardians agree to sign the informed consent forms voluntarily; 3. Infant's legal guardians are able to comply with the requirements of the clinical trial protocol; 4. Armpit temperature ≤ 37.0 ℃ Exclusion Criteria: 1. preterm birth (gestational age \< 37 weeks); 2. the presence of congenital malformations, developmental disorders, genetic defects, or severe malnutrition; 3. had a history of poliomyelitis; 4. had a personal or family history of allergy, convulsions, epilepsy, encephalopathy, or psychiatric disorders; 5. had known hypersensitivity to any component of the study vaccine or a history of severe allergic reaction (e.g., anaphylaxis) to any previous vaccination; 6. had immunodeficiency or receipt of immunosuppressive therapy; 7. diagnosed coagulation disorders (including factor deficiencies, coagulopathies, platelet abnormalities) or evidence of significant bruising/bleeding diathesis; 8. had known or investigator-suspected concurrent acute or active chronic diseases (including respiratory, cardiovascular, hepatic, renal, or dermatological conditions) or acute infection, or maternal HIV infection; 9. occurrence of fever (axillary temperature ≥ 38.0 °C) within the 3 days preceding enrollment; 10. had acute illness requiring systemic antibiotic or antiviral treatment within the 7 days preceding enrollment; 11. administration of blood products within the 3 months preceding enrollment; 12. had receipt of any live attenuated vaccine within the 14 days preceding enrollment; 13. had receipt of any inactivated or subunit vaccine within the 7 days preceding enrollment; 14. had recent administration of any other experimental product and any other condition deemed by the investigator as potentially interfering with the assessment of trial outcomes.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Jiangsu Provincial Center for Diseases Control and Prevention

    Nanjing, Jiangsu, 210009, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.