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Scientists create controlled whooping cough infection to speed up vaccine research

NCT ID NCT05136599

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 04, 2026 · Updated 2 times

Summary

This completed phase 1 study tested whether giving healthy adults a controlled dose of whooping cough bacteria via nasal spray can safely cause mild infection. The goal was to establish a human infection model for future vaccine and treatment research. 79 participants aged 18-40 were enrolled to find the optimal dose that causes mild symptoms without serious harm.

What this could mean

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

Active substance
Bordetella pertussis bacteria (intranasal)
What this could lead to
If successful, this model could help researchers test future pertussis vaccines and treatments more efficiently.
What could go wrong
This is an early-phase study with only 79 healthy adults, so results may not apply to the general population. The infection is mild and controlled, but risks include developing pertussis symptoms.

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 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

79 people

The number who actually took part.

Started

Jan 2022

Finished

Mar 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

18 to 40 years

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: To be eligible for the study, each participant must satisfy ALL of the following criteria: 1. Age 18-40 years, inclusive. 2. Good general health status, as determined by history and physical examination conducted no longer than 30 days prior to the challenge. 3. Participants who, in the opinion of the Investigator, can and will comply with the requirements of the protocol (e.g., complete Diary Cards, return for follow-up visits). 4. Written informed consent obtained from the participant. 5. If female of childbearing potential and heterosexually active, has practiced adequate contraception for 28 days prior to challenge and has a negative pregnancy test on the day before B. pertussis challenge and has agreed to continue adequate contraception until 60 days after inoculation. Adequate contraception is defined as a contraceptive method with a failure rate of \<1% per year when used consistently and correctly and, when applicable, in accordance with the product label. Examples include the following: * Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation: oral, intravaginal, or transdermal * Progestogen-only hormonal contraception associated with inhibition of ovulation: oral, injectable, or implantable * Intra-uterine device (IUD) with or without hormonal release * Vasectomized partner, provided that this is the participant's sole partner and that he has received a medical assessment of the surgical success * Credible self-reported history of heterosexual abstinence for at least 28 days prior to challenge * Female partner A premenopausal woman who has at least one of the following is considered not of childbearing potential: * Documented hysterectomy * Documented bilateral salpingectomy * Documented bilateral oophorectomy * Documented and current bilateral tubal ligation or occlusion 6. Currently fully vaccinated against SARS-CoV-2/COVID-19 according to provincial Public Health guidelines. 7. If there is a reported history of SARS-CoV-2/COVID-19 infection, the participant must be asymptomatic for \>4 weeks. Exclusion Criteria: Participants with ANY of the following criteria at the time of screening will be excluded: 1. Underlying chronic medical condition requiring ongoing follow-up and monitoring by a physician (e.g., diabetes, seizure disorder). 2. Underlying cardiac and/or pulmonary disease including hypertension, angina, prior myocardial infarction, asthma, emphysema, chronic bronchitis, and pulmonary tuberculosis. 3. Moderate or severe symptoms of health anxiety, anxiety, and mood symptoms. Self-reported current diagnosis of a major psychiatric illness, including a schizophrenia spectrum disorder, bipolar disorder, posttraumatic stress disorder, obsessive compulsive disorder, substance use, or eating disorder. 4. QT prolongation on electrocardiogram (EKG). 5. History of everyday smoking/vaping in the last 2 years and/or current smoking/vaping more than once per week. 6. Pregnant (known before or established at the time of screening using a urine-based test) or breastfeeding. 7. Immunocompromised (with HIV/AIDS-positive or receiving immunosuppressive therapy involving steroids) or with any medical condition or medication that leads to a compromised immune system. 8. Positive for hepatitis B or C. 9. Vaccinated against pertussis within previous 5 years and/or \>7 cumulative doses from infancy to date of screening. 10. Reported history of laboratory-confirmed pertussis infection. 11. Antibody titer to pertussis toxin \>20 EU/mL (2x the lower limit of quantification (LLOQ)). 12. Nasopharyngeal detection of B. pertussis prior to challenge using culture isolation and/or PCR detection, or detection of other respiratory infection. 13. Living with young children (\<1 year of age) or with any household member not current in their pertussis immunization up to Day 56 post-challenge. Note: Household members whose vaccination is not current will be offered a pertussis-containing vaccine, as recommended and funded by the Nova Scotia Department of Health and Wellness. 14. Living or working with (any form of close contact) any of the at-risk/vulnerable groups (children \<1 year of age, pregnant woman who have not yet received their maternal Tdap vaccine, immunocompromised individuals, anyone not current in their pertussis immunization, or adults \>65 years of age who have not received a dose of Tdap vaccine within the past 10 years) up to Day 56 post-challenge. 15. Known allergy to macrolides including azithromycin or erythromycin, history of Clostridium difficile within last 2 months. 16. Any contraindication to receiving azithromycin. 17. Taking any antibiotic currently or within the previous 2 weeks. 18. Currently taking terfenadine, astemizole, theophylline, or cimetidine. 19. Recent (within 6 months) nasal or sinus surgery, recent use of intranasal steroids (4 weeks), or diagnosis with nasal polyps. 20. Receipt of any investigational drug or vaccine (including SARS-CoV-2/COVID-19 vaccine) within 6 months prior to challenge. An investigational vaccine is defined as a vaccine that is still being tested in clinical trials or one that has not yet been authorized for use in Canada for administration by public vaccine programs. 21. Receipt of any authorized vaccines within 2 weeks of being challenged with B. pertussis in this study. (This is to avoid attributing any AEs from these vaccines to the B. pertussis challenge, which would skew the study results.) 22. Current laboratory-confirmed SARS-CoV-2/COVID-19 infection. 23. Previous moderate or severe laboratory-confirmed SARS-CoV-2/COVID-19 infection that required hospitalization. 24. Head trauma (e.g., fracture of the cribriform plate) within 1 year of screening. 25. Any other finding that the Investigator considers will make the participant unsuitable for the study or unable to comply with the study requirements. 26. Symptoms indicative of acute respiratory illness (such as fever, cough, difficulty breathing) identified during the physical examination done on Day -1 (check-in) or Day 0 before a participant is challenged. 27. History of Bell's Palsy and/or facial paralysis. 28. Receipt of facial cosmetic filler in the past 3 months.

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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

  • Canadian Center for Vaccinology

    Halifax, Nova Scotia, B3K 6R8, Canada

More trials for these conditions

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