Phase 1 Clinical Trial of the Safety and Immunogenicity of an Adenovirus-based TB Vaccine Administered by Aerosol

Tuberculosis Clinical Trial

Official title:

Phase 1, Open-label Clinical Trial to Evaluate the Safety and Immunogenicity of an Adenovirus-based Tuberculosis Vaccine Administered by Aerosol

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02337270
• Other study ID #: M002
• Status: Completed
• Phase: Phase 1
• Start date: September 5, 2017
• Est. completion date: September 7, 2021

Study information

• Verified date: October 2021
• Source: McMaster University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 1 study, in healthy volunteers who have previously been immunized with bacilli Calmette Guerin (BCG), to evaluate the safety and immune responses that develop in the blood and lungs following the administration by aerosol of a new experimental adenovirus-based vaccine for tuberculosis (TB), Ad5Ag85A.

Description:

This is a phase 1, open label study to evaluate the safety and immunogenicity of a single administration of one of two doses of a recombinant replication deficient human adenoviral (Ad5) TB vaccine containing the immunodominant antigen Ag85A delivered to the respiratory tract by aerosol in healthy volunteers with a history of BCG immunization. 28 healthy volunteers will be enrolled. The first cohort (n=8) will receive a lower dose of vaccine using the AeroNeb Solo Vibrating Mesh Nebulizer. For the second cohort (n=20) participants will be randomized to either a higher dose of vaccine by aerosol (n=10) or intramuscular administration (n=10). Cellular immune responses in the lung and peripheral blood will be evaluated

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: September 7, 2021
• Est. primary completion date: September 7, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Healthy human subjects who are between 18 and 55 years of age with a history of BCG vaccination.

2. HIV antibody negative

3. Able to understand and comply with protocol requirements and instructions; able to attend scheduled study visits and complete required investigations.

4. For women, negative pregnancy test and practicing two acceptable forms of contraception for the duration of the study (barrier contraceptive, birth control pill, surgically sterile, post-menopausal 2 years, abstinence)

5. For men, using barrier contraception for the duration of the study

Exclusion Criteria:

1. Pregnant or lactating women

2. Subjects who have any acute or chronic illnesses including active tuberculosis, any relevant findings on physical examination or are receiving any drug treatment in the opinion of the investigator likely to affect the immune system including current use of inhaled or nasal steroids.

3. Subjects with a history of any bleeding disorder or receiving any drug treatment that in the opinion of the investigator may increase the risk of bleeding

4. Subjects with a history of respiratory disease, e.g. asthma, chronic bronchitis, chronic obstructive pulmonary disease (COPD).

5. Current smokers, including e-cigarettes, and ex-smokers who have quit within the last year, as reported by the subject

6. Subjects with clinically significant abnormality of baseline spirometry tests

7. Any health-related condition for which study bronchoscopy is contraindicated

8. Subjects who have a history of active or latent TB infection or whose PBMC's are responsive to ESAT6/CFP10 stimulation using a commercial interferon gamma release assay for TB [consistent with latent TB infection].

9. Subjects whose baseline laboratory values are outside of the normal range unless the abnormality is considered not to be of clinical relevance by the Investigator. A single repeat test is allowed during the screening period.

10. Subjects whose use of alcohol or drugs would, in the opinion of the investigator, interfere with adherence to the study protocol.

11. Subjects who are using, or have a history of using, inhaled cocaine, metamphetamine or other inhaled or smoked recreational drugs. Subjects who give a history of last smoking marijuana more than a year ago may be enrolled, as long as they do not smoke marijuana for the duration of the study.

12. Failure to provide written consent.

13. Known allergy to vaccine components

14. Previous vaccination with Ad5Ag85A or any other experimental TB vaccine

15. Known exposure to active TB within past 6 months or subjects whose occupation puts them at increased risk of TB exposure (based on Hamilton Health Science/St Joseph Healthcare list of high risk personnel)

16. Any abnormality on chest x-ray suggestive of active or remote tuberculosis infection or evidence on chest-x-ray of clinically significant respiratory disease.

17. PPD skin test within last 12 months

Related Conditions & MeSH terms

• Adenoviridae Infections
• Tuberculosis

Intervention

Biological:
• Ad5Ag85A
Aerosol administration of Ad5Ag85A

Locations

Country	Name	City	State
Canada	McMaster University Medical Centre	Hamilton	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
McMaster University	Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants reporting adverse events	Adverse events will be assessed according to the CTCAE Expanded Common Toxicity Criteria at 48-72 hours after vaccination, and at weeks 2, 4, 8, 12, 16 and 24	Over 24 weeks
Secondary	Immunogenicity of one of two doses of Ad5Ag85A administered by aerosol	Change from baseline in the immune responses of specific T-cells in bronchoalveolar lavage [BAL] fluid (mucosal) and blood (systemic). Immune responses measured will include interferon Elispot assay, cytokine production and intracellular cytokine staining	Two weeks after vaccination
Secondary	Immunogenicity of one of two doses of Ad5Ag85A administered by aerosol		Eight (first cohort) or twelve (second cohort) weeks after vaccination
Secondary	Immunogenicity of inhaled administration of Ad5Ag85A compared with intramuscular administration		Two weeks after vaccination
Secondary	Immunogenicity of inhaled administration of Ad5Ag85A compared with intramuscular administration		Twelve weeks after vaccination
Secondary	Number of participants reporting adverse events with inhaled administration of Ad5Ag85A compared with intramuscular administration		Over 24 weeks
Secondary	Immune responses measured from induced sputum compared with bronchoalveolar lavage	For first cohort of 8 participants only	Two weeks after vaccination
Secondary	immune responses measured from induced sputum compared with bronchoalveolar lavage	For first cohort of 8 participants only	Eight weeks after vaccination
Secondary	Number of participants developing a positive interferon release assay for TB after vaccination with Ad5Ag85A	For first cohort of 8 patients only	At 16 weeks
Secondary	Number of participants reporting adverse events correlated with level of pre-existing anti-adenoviral antibodies		Over 24 weeks
Secondary	Immune response to vaccination correlated with pre-existing anti-adenoviral antibodies		Two weeks after vaccination
Secondary	Immune response to vaccination correlated with pre-existing anti-adenoviral antibodies		Eight weeks after vaccination
Secondary	Number of participants reporting adverse effects correlated with dose of vaccine received by inhalation		Over 24 weeks
Secondary	Immune response to vaccine correlated with dose of vaccine received by inhalation		Two weeks after vaccination
Secondary	Immune response to vaccine correlated with dose of vaccine received by inhalation		Eight or 12 weeks after vaccination

External Links

•   Safety and immunopotency of an adenovirus-vectored tuberculosis vaccine delivered via inhaled aerosol to healthy humans: a dose and route comparison phase 1b study