Intradermal Administration of a COVID-19 mRNA Vaccine in Elderly

NCT05977127 | Terminated Phase 2

• 1 other identifier: 2023-503800-99-00
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 1

Brief Summary

Respiratory tract infections, e.g. caused by SARS-CoV-2, disproportionately affect elderly. Vaccination has shown to be the most cost-effective approach to prevent infections. However, older adults often fail to induce a potent immune response to vaccines, as was also seen recently for COVID-19 mRNA vaccines. This is likely due to immune dysfunction as a consequence of aging. To potentiate a stronger immune response, vaccine administration into the papillary dermis (intradermal, ID) has been proposed as an alternative strategy to intramuscular (IM) administration. Vaccination through the ID route has shown to be safe and equally or more effective than IM vaccination with a wide variety of vaccines. Recently, ID administration has been tested with two COVID-19 mRNA vaccines (Spikevax, Moderna and Comirnaty, Pfizer/BioNTech) in reduced (fractional) doses of the standard IM dose. To ease ID administration and thereby facilitate the implementation of this route, silicon-based microneedles have been developed. These needles have shown to allow ID administration of the Spikevax vaccine with equal safety and immunogenicity profiles as the traditional Mantoux approach in young adults. In the present study, we will investigate the immunogenicity of a 20 mcg dose of the COVID-19 mRNA Comirnaty vaccine through ID administration with silicon microneedles in elderly people (75 years and older), and compare this to immunogenicity of IM administration of a 20 mcg dose and a 30 mcg (standard IM) dose.

Conditions

Vaccination; Infection; COVID-19

Keywords

Intradermal; COVID-19 mRNA vaccine; Elderly; Immune response

Outcome Measures

Primary Outcomes (1)

• Concentrations of SARS-CoV-2-Spike protein specific IgG antibodies in serum for the different intervention groups

  at 28 days after vaccination

Secondary Outcomes (2)

• Titers of SARS-CoV-2 specific neutralising antibodies in serum of the different intervention groups

  at 28 days after vaccination

• The percentage of participants with local and systemic adverse events

  up to 28 days after vaccination

Other Outcomes (5)

• Concentrations of SARS-CoV-2-Spike protein specific antibodies in serum and mucosal samples for the different intervention groups at various timepoints

  Day 0, day 28 and month 4 after vaccination

• Titers of SARS-CoV-2 specific neutralising antibodies in serum and mucosal samples of the different intervention groups at various timepoints

  Day 0, day 28 and month 4 after vaccination

• Changes in expression level of host genes

  day 0 and day 1 after vaccination

Study Arms (3)

Intradermal vaccination with 20 mcg mRNA vaccine

EXPERIMENTAL

Participants will receive a single dose of 20 mcg COVID-19 mRNA vaccine (Comirnaty; Pfizer/BioNTech) through the intradermal route using microneedles.

Biological: Comirnaty

Intramuscular vaccination with 30 mcg mRNA vaccine

ACTIVE COMPARATOR

Participants will receive a single dose of 30 mcg COVID-19 mRNA vaccine (Comirnaty; Pfizer/BioNTech) through the intramuscular route.

Biological: Comirnaty

Intramuscular vaccination with 20 mcg mRNA vaccine

ACTIVE COMPARATOR

Participants will receive a single dose of 20 mcg COVID-19 mRNA vaccine (Comirnaty; Pfizer/BioNTech) through the intramuscular route.

Biological: Comirnaty

Interventions

Comirnaty BIOLOGICAL

Administration of Comirnaty vaccine

Intradermal vaccination with 20 mcg mRNA vaccine; Intramuscular vaccination with 20 mcg mRNA vaccine; Intramuscular vaccination with 30 mcg mRNA vaccine

Eligibility Criteria

• Age: 75 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Older Adult (65+)

You may qualify if:

• Male or female aged ≥75 years at the moment of immunization.
• Healthy, determined by medical history and clinical judgement of the investigator. Participants with a pre-existing illness that is stable, defined as disease not requiring significant change in therapy or hospitalisation during the 6 weeks before enrolment and not expected to require any intervention during the study, can be included.
• Willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, and other study procedures.
• Willing to postpone their regular COVID-19 vaccination upon invitation by the Municipal Health Service or general practitioner until at least four months after receiving the intervention.
• Completed a primary series of COVID-19 vaccination.
• Capable and willing to give personal signed informed consent.
• Adequate understanding of the procedures of the study and agrees to abide strictly thereby.
• Fully conversant in the Dutch language.
• Agrees his/her general practitioner is informed about participation in the study.
• Agrees to provide access to information regarding their vaccination background.
• Agrees that the study physician and his/her delegates have access to their medical file at Radboudumc.

You may not qualify if:

• Medical or psychiatric condition that may increase the risk of study participation or, in the investigator's judgement, make the participant inappropriate for the study.
• No decision-making capacity.
• History of severe adverse reaction to a vaccine or to any component of the study intervention.
• Thrombose with thrombocytopenia syndrome after vaccination with a COVID-19 vaccine.
• Dermatological conditions that might interfere with the ID vaccination.
• Receipt of COVID-19 vaccination within 3 months before receiving the study intervention.
• Known or suspected immunodeficiency, as determined by medical history or medication use (inhalation corticosteroids are allowed).
• History of autoimmune disease or an active autoimmune disease requiring therapeutic intervention.
• Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate IM injection.
• Participation in other studies involving other study interventions within 28 days prior and during 28 days after receiving the study intervention.
• Receipt of any other non-study vaccine within 28 days prior and after receiving the study intervention.

Sponsors & Collaborators

• Radboud University Medical Center: lead

Study Sites (1)

Radboudumc

Nijmegen, Netherlands

Location

MeSH Terms

Conditions

Infections; COVID-19

Interventions

BNT162 Vaccine

Condition Hierarchy (Ancestors)

Pneumonia, Viral; Pneumonia; Respiratory Tract Infections; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

mRNA Vaccines; Nucleic Acid-Based Vaccines; Vaccines, Synthetic; Recombinant Proteins; Proteins; Amino Acids, Peptides, and Proteins; Vaccines; Biological Products; Complex Mixtures; COVID-19 Vaccines; Viral Vaccines; Antigens; Biological Factors

Study Officials

• Hans de Graaf

  Stichting Radboud University Medical Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Masking Details: Only laboratory personnel is masked. Because of the different administration routes it is not possible to mask the participants or investigators
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: open-label, randomised, proof-of-concept intervention study

Study Record Dates

• First Submitted: August 3, 2023
• First Posted: August 4, 2023
• Study Start: September 26, 2023
• Primary Completion: March 21, 2024
• Study Completion: March 21, 2024
• Last Updated: March 28, 2024

Record last verified: 2024-03

Locations

NL (1)