Clinical Trial

pH1N1 Blinded Challenge Study

Recruiting Phase 1
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Summary
This protocol describes a clinical trial to develop and validate a Controlled Human Infection Model (CHIM) for influenza A/Arkansas/08/2020 (pH1N1). The study is designed to determine the optimal infectious dose of the pH1N1 challenge strain for use in future clinical trials evaluating influenza countermeasures. The study will enroll and challenge adult volunteers with the pH1N1 influenza virus challenge or sham inoculations. Given the adaptive design of this trial, the potential number of participants can vary. Depending on the pathway recommended by the PSRT and followed in the Trial Schema, the study population can range from around 30 to 99. The anticipated final sample size will be approximately 90 receiving pH1N1 challenge product plus and 6 persons receiving a sham inoculation. Participants will be pre-screened for health and for serological HAI antibody titers of \</1:40 against the challenge strain. Eligible participants will be enrolled sequentially into challenge cohorts and will be randomly assigned to receive a single dose of either sham inoculation or the interventional study product at a dose between 10\^6 to 10\^7 TCID50 (or 10\^5 TCID50 if needed). Dose titration will be conducted under an adaptive escalation schedule whereby dosing will start at 10\^6 TCID50 and escalate to the next dose if a pre-determined symptomatic influenza attack rate and clinical symptom score thresholds are not met and if the dose is determined to be safe with no pre-defined halting criteria being met. The primary objectives of this study are to determine the optimal infectious dose of a pH1N1 viral challenge to cause laboratory-confirmed clinical influenza and to assess the safety profile of pH1N1 viral challenge.
Protocol Amendment History 5 changes
notable Primary completion pushed: 2026-06-23 -> 2026-10-10 2026-07-07
minor Completion pushed: 2026-08-18 -> 2026-10-10 2026-07-07
critical Primary endpoint(s) modified 2026-04-09
notable Enrollment reduced: 180 -> 90 participants 2026-04-09
minor Trial arms changed: 9 -> 12 2026-04-09
Trial Details
NCT Number NCT07110532
Lead Sponsor National Institute of Allergy and Infectious Diseases (NIAID)
Conditions Influenza
Enrollment 90 participants
Start Date 2025-09-10
Primary Completion 2026-10-10 (estimated)
Study Completion 2026-10-10 (estimated)
Updated on ClinicalTrials.gov 2026-07-24