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New COVID vaccine shows promise in both needle and nasal spray forms

NCT ID NCT05205746

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a single dose of a new COVID-19 vaccine (AVX/COVID-12) in 158 healthy adults who already had some immunity to the virus. The vaccine was given either as an injection or a nasal spray to see which route worked better and was safe. Researchers measured antibody and T-cell responses to understand how well the vaccine boosted protection.

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 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

158 people

The number who actually took part.

Started

Nov 2021

Finished

Jul 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

18 years and older

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. Be ≥ 18 years old. 2. Indistinct sex. 3. Having given their informed consent. 4. No respiratory problems during the last 21 days prior to administration of the single dose. 5. No conditions or alterations in the physical examination, laboratory values and cabinet that in the opinion of the investigator may interfere with the participation of the subject in the study or require a more detailed medical study. 6. Negative PCR test for SARS-CoV-2 during the screening visit. 7. Negative pregnancy test in women with pregnancy potential. 8. Signature of commitment for the use of highly effective contraceptive methods for at least 30 days after administration of the intramuscular injection or intranasal. 9. In case of presenting any chronic disease with medical management, it must be controlled and stable without changes in treatment during the last three months prior to the scrutiny visit. 10. Commitment to maintain adequate prevention measures to avoid the contagion by SARS-CoV-2 during their participation in the study, considering themselves these strict use during the first 14 days after the baseline visit (Use of face masks in closed places, social distancing measures in spaces open, and frequent hand washing). 11. Present detectable titers of anti-Spike IgG in peripheral serum during the visit of screening with titers less than 1,200 U/mL in a chemiluminescence test. 12. Submit proof of vaccination 4 months or more after the last vaccination 13. Have been vaccinated with the complete program of any of the following vaccines against SARS-CoV-2: * ModeRNA * Pfizer * AstraZeneca * CanSino * Sinovac * Sinopharm * Johnson \& Johnson (Janssen) * Sputnik V Exclusion Criteria: 1. History of hypersensitivity or allergy to any of the components of the vaccine. 2. History of severe anaphylactic reactions from any cause. 3. History of seizures. 4. Uncontrolled chronic diseases. 5. Chronic diseases that require management with immunosuppressive agents or immune response modulators (eg, systemic corticosteroids, cyclosporine, rituximab among others). 6. Oncological disease. 7. Active participation, or during the last 3 months in any other clinical study or research experimental intervention. 8. Use within 30 days prior to screening evaluation of any drug or herbal supplement, or alternative medicine (for example, transfer factor, chlorine dioxide, etc.) aimed at treating or preventing complications or contagion by SARS-CoV-2, or any other condition. 9. Febrile illness at the time of the screening visit. 10. Have received any vaccine (experimental or approved) during the 60 days prior to the scrutiny visit. 11. Having received a blood transfusion or blood components during the last 4 months prior to the scrutiny hearing. 12. Have been a plasma donor during the last 4 months prior to the visit of scrutiny. 13. Have undergone dialysis or hemodialysis procedures during the last year prior to the scrutiny visit. 14. Work on poultry or gamecock farms. 15. History of substance abuse problems that in the opinion of the investigator could interfere with the subject's ability to adequately comply with the protocol guidelines.

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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

  • CAIMED Investigación en Salud S.A. de C.V.

    Mexico City, Mexico City, 06760, Mexico

  • Centro Mexicano de Estudios Clínicos CEMDEC SA de CV

    Mexico City, Mexico City, 06100, Mexico

  • Oaxaca Site Management Organization S.C.

    Oaxaca City, Oaxaca, 68000, Mexico

  • Unidad Médico Familiar No. 20 Instituto Mexicano del Seguro Social

    Mexico City, Mexico City, 07760, Mexico

More trials for these conditions

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