RecruitingPhase 2NCT07215858

BPL-1357 Against H1N1 Influenza Virus Challenge

Randomized, Double-Blinded, Placebo-Controlled, Phase 2 Study of the Safety and Efficacy of BPL-1357 Against H1N1 Influenza Virus Challenge


Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Enrollment

129 participants

Start Date

Jul 29, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Background: Influenza (flu) infections are a serious global health threat. Each year, between 3 and 5 million people get the flu, and up to 500,000 die from it. Current vaccines protect against seasonal flus, but broader vaccines are needed to protect against potential flu pandemics. Objective: To test an experimental flu vaccine. Eligibility: Healthy people aged 18 to 55 years. Design: The study will last 5 to 8 months and has 2 phases, A and B. The study vaccine will be given either as a shot in the arm or as a nasal spray. Participants will receive 1 of 3 combinations: (1) study vaccine in the nose and placebo in the arm; (2) placebo in the nose and study vaccine in the arm; or (3) placebo in the nose and placebo in the arm. A placebo is just like the real vaccine but contains no active ingredients. Phase A: Participants will have 5 clinic visits over 56 days. They will receive a shot and a nasal spray at 2 of the visits, 28 days apart. At each visit, they will have a physical exam, with tests of their blood, urine, and nasal secretions. They will check their temperature at home and record any symptoms for 7 days after each vaccine. Phase B: Participants will stay in the hospital for at least 9 days. They will be infected with a flu virus. They will provide blood, urine, and nasal fluid samples. They will have tests of their heart function. They will remain in the hospital until they test negative for the flu 2 days in a row. They will have 2 follow-up visits, 4 and 8 weeks after leaving the hospital. ...


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called BPL-1357 IM, a biological treatment called BPL-1357 IN, and others for people with human and influenza. The study is currently recruiting participants at 2 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALBPL-1357 IM

Quadrivalent, inactivated, whole-virus vaccine containing 4 different wild-type avian viruses given intramuscularly.

BIOLOGICALBPL-1357 IN

Quadrivalent, inactivated, whole-virus vaccine containing 4 different wild-type avian viruses given intranasally.

OTHERPlacebo IM

Placebo given intramuscularly.

OTHERPlacebo IN

Placebo given intranasally.


Locations(2)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

University of Texas Medical Branch, Galveston

Galveston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07215858


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