Vaccine Pandemic Preparedness Through Airway Immunology Characterization (VAXXAIR)

Chronic Obstructive Pulmonary Disease Trial Network, Denmark

Status and phase: Begins enrollment in 2 months; Early Phase 1

Conditions: Influenza, Human

Treatments: Biological: Vaxigripetra; Biological: Flumist

Study type: Interventional

Funder types: Other

Identifiers

NCT05921448

VAXXAIR

Details and patient eligibility

About

The study aims to compare the effectiveness of live attenuated influenza vaccines (LAIV) and intramuscular-inactivated vaccines (IIV) in healthy individuals aged 18-49. It will investigate cellular and humoral responses, identify immunological markers for targeted vaccine improvement, and establish a collaborative platform for accelerated immunological and clinical vaccine research.

Full description

There are several types of vaccines and the focus on the important role of vaccines in health has increased after the SARS-CoV-2 pandemic. Therefore, it is desired to investigate whether so-called 'live attenuated influenza vaccines' (LAIV) can prove more effective than the most frequently used 'intramuscular-inactivated vaccines' (IIV).

Several studies have previously compared the humoral and cellular response to LAIV and IIV and some of these have shown that LAIV elicits a more robust cellular response than intramuscularly administered vaccines.

In the study, the immunological differences in cellular and humoral response following vaccination either intramuscularly or nasally will be characterized. The patient group will consist of healthy individuals between 18-49 years of age. It is further desired to identify immunological markers that vaccines can be directed against in order to improve the immunological response. Finally, a platform for collaboration on accelerated immunological and clinical vaccine research will be established.

The study is a randomized, double-blind, placebo-controlled study. It is carried out in several locations and is Good Clinical Practice monitored.

Enrollment: 60 estimated patients

Sex: All

Ages: 18 to 49 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Healthy individuals (Charlson´s co-morbidity index :0, and investigator judged as healthy)

2. Age: 18-49 years

3. Total IgG levels in normal range (discretion of investigator according to local lab)

4. Total IgA levels (discretion of investigator according to local lab)

5. Undetectable HAI titres to the H3N2 component of the vaccines*

6. Normal CD4+ and CD8+ T-cell and normal B-cell counts

7. Reference levels from ISO-15189 accredited T-, B- and NK-cell count routine analyses will be applied.

   • If <20% of the first 100 screened persons apply to this criterion, this will be changed to a specific cut off based on the lowest quartile level of HAI titres to the H3N2 component of these 100 screened persons.

Exclusion criteria

1. Laboratory-confirmed influenza infection during the past year documented by a positive PCR test in the Danish Microbiological database or anamnestic reported influenza infection in the same period

2. Active smoker

3. BMI > 35 kg/m2

4. Women of childbearing potential not using safe contraception, or who are pregnant, or breast-feeding

5. Any allergies to components of or contraindication for Vaxigriptetra® or Flumist® incl. previous severe adverse reactions to influenza vaccinations or components of the vaccines

6. Use of immunosuppressive drugs* within the past 6 months or who are currently using them

7. HIV, HBV, HCV laboratory confirmed active infection at screening visit

8. Have an acute illness, including an oral temperature ≥ 38°C, within 3 days prior to vaccination

9. Have received any vaccines, including live-attenuated vaccines within 4 weeks before inclusion, or plan receipt of such vaccines within 30 days following the inclusion

10. Any known malignant neoplasm within 5 years (except basal carcinoma of the skin).

11. Severe mental illness or linguistic issues which significantly impedes cooperation

12. Inability to provide written informed consent

    • defined as: Azathioprin, methotrexate, cyclophosphamide, basiliximab, belimumab, anifrolumab, alemtuzumab, rituximab, mycophenolat, calcineurin inhibitors (ciclosporin, voclosporin and tacrolimus), mTOR inhibitors (everolimus and sirolimus), prednisolone (or any corticosteroid in doses above the equivalent of 5 mg prednisolone), TNF-α inhibitors (such as infliximab), anti-thymocyte globulin.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 2 patient groups

Vaxigripetra

Experimental group

Description:

This arm will receive 1 dose of 0.5 mL Vaxigripetra (intra-muscular injection) and 1 dose of 0.2 mL placebo (nasal, 1 spray in each nostril).

Treatment:

Biological: Vaxigripetra

Flumist

Experimental group

Description:

1 dose of 0.2 mL Flumist (nasal, 1 spray in each nostril) and 1 dose of 0.5 mL placebo (intra-muscular injection).

Treatment:

Biological: Flumist