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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06972810




Registration number
NCT06972810
Ethics application status
Date submitted
27/04/2025
Date registered
15/05/2025
Date last updated
12/06/2025

Titles & IDs
Public title
Human Infection Study of H3N2 Influenza in Healthy Adults
Scientific title
A Controlled Human Infection Study of a Recombinant H3N2 (A/Texas/71/2017, Clade 3C3a) Influenza Virus in Healthy Adults in Australia
Secondary ID [1] 0 0
27338
Universal Trial Number (UTN)
Trial acronym
FluCHIM
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Influenza 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - A/Texas/71/2017, clade 3C3a H3N2 influenza virus

Experimental: Influenza Challenge Model with Influenza A H3N2 virus strain -


Other interventions: A/Texas/71/2017, clade 3C3a H3N2 influenza virus
The intervention product is a live challenge virus that is manufactured in the USA under Good Manufacturing Practice (GMP). The challenge will be administered intranasally using a sprayer device. Participants will be admitted into an inpatient facility prior to the administration of the flu virus. Following inoculation, they will be quarantined for a minimum of 8 days prior to discharge. Participants will receive supportive care and PCR positive participants will receive an effective antiviral medication. Participants will be followed for a total of 6 months.
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of participants who become infected with the virus
Timepoint [1] 0 0
Day 1 to Day 7 post challenge
Primary outcome [2] 0 0
Safety of the H3N2 challenge model
Timepoint [2] 0 0
Day 0 to 6 months post challenge
Secondary outcome [1] 0 0
Detection of asymptomatic infection
Timepoint [1] 0 0
Day 1 to 7 post challenge
Secondary outcome [2] 0 0
Percentage of participants who develop influenza antibodies
Timepoint [2] 0 0
Day 0 - 14 post challenge

Eligibility
Key inclusion criteria
1. General good health, without significant medical conditions that would interfere with participant safety, as defined by medical history, physical examination, screening laboratory tests, and ECG at a screening evaluation.
2. Susceptible to the challenge virus as determined by a baseline serum HAI and NAI antibody titer to the RG-A/Texas/71/2017 (H3N2; clade 3c3a) virus of 1:40 or less.
3. Able to understand and comply with planned study procedures and available for the duration of the trial.
4. Willing to participate in the study and adhere to all trial requirements, including providing written consent to remain at the trial site for at least seven days after administration of the challenge virus. This willingness must be demonstrated by signing the informed consent document.
5. Willing to allow the investigators to discuss the participant's medical history with their General Practitioner or any relevant health professional.
6. Willing to refrain from donating blood for the duration of the study period.
7. Willing to refrain from smoking and illicit drug use during the quarantine period.
8. Women of childbearing potential (WOCBP)* are required to practice a highly effective form of contraception during the course of the study. Acceptable forms of contraception for female participants include:

1. Established use of oral, injected or implanted hormonal methods of contraception (established for a minimum of 4 weeks prior to first inpatient quarantine).
2. Placement of an intrauterine device (IUD) or intrauterine system (IUS).

* Male sterilization, if the vasectomized partner is the sole partner for the participant and appropriate post vasectomy documentation of sterilization success is available.
3. Same sex intercourse only.
4. True abstinence from heterosexual intercourse, when this is in line with the preferred and usual lifestyle of the participant (Periodic abstinence and withdrawal are not acceptable methods of contraception). Careful history and documentation regarding the reliability of this method must be recorded.
Minimum age
18 Years
Maximum age
50 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
1. History of clinically significant or currently active neurological, cardiac, respiratory, hepatic, rheumatological, autoimmune, or renal disease. Specifically:

1. History of chronic obstructive pulmonary disease, pulmonary hypertension, or chronic lung condition of any etiology;
2. Current diagnosis of asthma or reactive airway disease (e.g., to viral infections) within the past 2 years;
3. History of thromboembolic, cardiovascular or cerebrovascular disease;
4. Current diabetes mellitus (Type I or Type II);
5. Any history of malignancy except for non-recurrent basal cell carcinoma;
6. History or evidence of clinically significant autoimmune disease or known immunodeficiency of any cause (including HIV);
7. History of a surgical splenectomy;
8. History of severe psychiatric illness at any time (e.g., psychiatric illness that resulted in inpatient admission, psychosis, suicide attempt) or current significant active symptoms of anxiety and/or depression; i. Participants with history of anxiety-related symptoms of any severity within the last 2 years if the Generalized Anxiety Disorder-7 score is =5 ii. Participants with a history of depression of any severity within the last 2 years if the Patient Health Questionnaire-9 score is =4
9. Bleeding disorder (e.g., factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following injections or venepuncture; OR
10. Other conditions that, in the opinion of the Investigator, could interfere with a participant completing the study and necessary investigations.
2. Any clinical laboratory test parameters = 1.5x upper limit of normal (ULN) unless deemed by the investigator to have no clinical significance.
3. Body Mass Index (BMI) of less than 18.5 or greater than 32.
4. Behavioral or cognitive impairment that in the opinion of the investigator affects the ability of the participant to understand and cooperate with the study protocol.
5. The use of alcohol or psychoactive drugs/controlled substances in the past 12 months that:

1. Has had a functional impact on the participant's life;
2. Has resulted in or been a medical condition that required treatment; OR
3. Could constitute abuse or misuse
6. Current use of illicit substance use, defined as a negative urine drug screen at screening and at admission (cannabis (THC), amphetamine, barbiturates, benzodiazepines, cocaine, ecstasy, methamphetamine, methadone, opiates, Phencyclidine (PCP)).
7. History of anaphylaxis.
8. Allergy to both Oseltamivir and Baloxavir.
9. Known allergy to two or more classes of antibiotics (e.g., penicillins, cephalosporins, fluoroquinolones, or glycopeptides).
10. Personal or family history a severe response to a viral infection including but not limited to:

1. Guillain-Barré Syndrome;
2. Clinically significant post-viral fatigue or other post-viral long-term sequalae.
11. Previous hospitalization with influenza or related complications.
12. Use of corticosteroids (including nasal sprays/inhaled preparations but excluding other topical preparations) or immunosuppressive drugs within 30 days prior to challenge.
13. Receipt of a live vaccine within 4 weeks or other vaccine within 2 weeks prior to enrollment.
14. Receipt of any investigational drug or vaccine within 3 months or 5.5 half-lives (whichever is greater).
15. Receipt of blood or blood-derived products (including immunoglobulin) within 6 months prior to challenge.
16. Smoking or vaping:

1. Current smoker defined as anyone who has smoked a nicotine product (including any vaping) at anytime in the month prior to enrollment; OR
2. Significant past history of smoking (defined as = 20 year pack history and ceased smoking <10 years ago).
17. Participants who share a household with someone at higher risk for influenza-related complications, including:

1. Persons =65 years of age or <5 years of age;
2. Persons with chronic pulmonary disease (e.g., asthma), chronic cardiovascular disease (e.g., cardiomyopathy, congestive heart failure, ischemic heart disease), metabolic disease (e.g., diabetes mellitus, renal dysfunction, haemoglobinopathies), immunosuppression, neurological and neurodevelopmental conditions,
3. Children and teenagers who are receiving long-term aspirin therapy, OR
4. Women who are pregnant or who are trying to become pregnant.
18. Infection with human immunodeficiency virus-1 (HIV-1), hepatitis C virus (HCV), or hepatitis B (HBV)
19. Clinically significant abnormalities on ECG (as determined by the study investigator).
20. Concurrent enrollment (or planned at anytime over the course of this trial) in a study which uses an investigational product or collects participant's blood.
21. Acute medical condition which is either undiagnosed/still being investigated at time of challenge, OR requiring new or adjustment of prescription medication use in the 30 days prior to challenge.
22. Any neurologic abnormality impairing the gag reflex or contributing to aspiration.
23. Significant abnormality altering the anatomy of the nose/nasopharynx or clinically significant nasal deviation or any other clinically significant nasal pathology.
24. Recent history (180 days prior to challenge) of nasal/sinus surgery or epistaxis requiring a medical procedure to control it (e.g., cauterisation, packing, the use of topical vasoconstrictors).
25. Current sinusitis.
26. Venous access deemed inadequate for the phlebotomy demands of the study.
27. Confirmed infection with influenza virus (on PCR) within the past 6 months prior to enrollment.
28. Receipt of a seasonal influenza vaccine in the past 6 months prior to enrollment or planned receipt in the first 2 months of the study.
29. Any condition or finding, to include medical and psychiatric conditions, that in the opinion of the Investigator, might interfere with the safety of the participant, affect the participant's ability to participate in the trial and/or interfere with the collection or interpretation of the study objectives.
30. Participants who are excluded from the study because they have been discovered during screening procedures to be suffering from a previously undiagnosed condition thought to require further medical attention will, with their consent, be referred appropriately to their GP or a specialist.

Study design
Purpose of the study
Other
Allocation to intervention
Not applicable
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
5/05/2025
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
30/06/2026
Actual
Sample size
Target
12
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Doherty Clinical Trials - Melbourne
Recruitment postcode(s) [1] 0 0
3002 - Melbourne

Funding & Sponsors
Primary sponsor type
Other
Name
University of Melbourne
Address
Country
Other collaborator category [1] 0 0
Government body
Name [1] 0 0
National Institute of Allergy and Infectious Diseases (NIAID)
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Other
Name [2] 0 0
WHO Collaborating Centre for Reference and Research on Influenza
Address [2] 0 0
Country [2] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Dr Gail Cross, MBSS (BSc), FRACP
Address 0 0
University of Melbourne
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Dr Gail Cross, MBSS (BSc), FRACP
Address 0 0
Country 0 0
Phone 0 0
+61 (0) 3 9970 4200
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided


Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT06972810