H3N2 M2SR in Pediatric Population

Completed · Phase 1 · Has a placebo group

Conditions studied: Influenza, Influenza Immunisation

In brief

This is a Phase I double-blind, randomized, placebo-controlled study in 50 healthy adolescents and children, 9-17 years of age, inclusive, who are in good health and meet all eligibility criteria. This clinical trial is designed to assess the safety and immunogenicity of a prime-boost regimen of H3N2 M2SR intranasal influenza vaccine (manufactured by FluGen) followed by licensed inactivated Quadrivalent Influenza Vaccine (QIV) boost administered intramuscularly Subjects will be enrolled in one of two groups in a 1:1 ratio. Arm 1 will receive one dose of M2SR intranasally on Day 1 and one dose of QIV on Day 92. Arm 2 will receive one dose of placebo (saline) intranasally on Day 1, and one dose of QIV on Day 92. Study duration will be approximately 28 months with patient participation duration approximately 13 months. The primary study objective is to assess the safety and reactogenicity of a monovalent live attenuated influenza H3N2 M2SR vaccine.

Key facts

Study ID

NCT03553940

Run by

National Institute of Allergy and Infectious Diseases (NIAID)

People needed

43

Starts

2018-08-15

Expected to finish

2020-08-27

Last updated by the study team

2021-10-21

Who can join

Age: 9 and older, up to 17. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Parent(s)/legal guardian(s) must provide written informed consent prior to initiation of any study procedures, and subject must provide assent.
• Are able to understand and comply with planned study procedures and be available for all study visits.
• Are males or non-pregnant females, 9-17 years old, inclusive at the time of enrollment.
• Are in good health*.
• As determined by medical history and physical examination to evaluate acute or currently ongoing chronic medical diagnoses or conditions, defined as those that have been present for at least 90 days, which would affect the assessment of the safety of subjects or the immunogenicity of study vaccinations. Chronic medical diagnoses or conditions should be stable for the last 60 days (no hospitalizations, ER, or urgent care for condition and no adverse symptoms that need medical intervention). This includes no change in chronic prescription medication, dose, or frequency as a result of deterioration of the chronic medical diagnosis or condition in the 60 days prior to enrollment. Any prescription change that is due to change of health care provider, insurance company, etc., or that is done for financial reasons, as long as in the same class of medication, will not be considered a deviation of this inclusion criterion. Any change in prescription medication due to improvement of a disease outcome, as determined by the site principal investigator or appropriate sub-investigator, will not be considered a deviation of this inclusion criterion. Subjects may be on chronic or as needed (prn) medications if, in the opinion of the site principal investigator or appropriate sub-investigator, they pose no additional risk to subject safety or assessment of reactogenicity and immunogenicity and do not indicate a worsening of medical diagnosis or condition. Similarly, medication changes subsequent to enrollment and study vaccination are acceptable provided there was no deterioration in the subject's chronic medical condition that necessitated a medication change, and there is no additional risk to the subject or interference with the evaluation of responses to study vaccination. Note: Low dose topical steroids, herbals, vitamins, and supplements are permitted.
• Oral temperature is less than 100.0 degrees Fahrenheit.
• For female adolescent of child-bearing potential* must agree to correctly use an acceptable method of contraception** from 30 days prior to vaccination until 30 days after the last study vaccination.
• Defined by the onset of menses, and not sterilized via tubal ligation, bilateral oophorectomy, hysterectomy, or successful Essure(R) placement (permanent, non-surgical, non-hormonal sterilization) with documented radiological confirmation test at least 90 days after the procedure, and still menstruating.
• *Includes non-male sexual relationships, abstinence from sexual intercourse with a male partner, monogamous relationship with a vasectomized partner, and correct use of male condoms with the use of applied spermicide, intrauterine devices, NuvaRing(R), and licensed hormonal methods such as implants, injectables, contraceptive patches or oral contraceptives ("the pill"). Method of contraception will be captured on the appropriate data collection form.
• Female adolescent of childbearing potential must have a negative urine pregnancy test within 24 hours prior to study vaccination.
• Males who are sexually active with a female of childbearing potential must agree not to father a child for 30 days after receipt of the first study vaccination.
• Agrees not to participate in another clinical trial during the study period.
• Agrees not to donate blood or blood products to a blood bank for 12 months after receiving the investigational vaccine.
• Weight = / > 34 kg or 75 pounds.
• Hemoglobin = / > 11.5 g/dL.
• Hematocrit > 35%.
• Ferritin level = / > 15 ng/mL.
• Parent/legal guardian must provide consent to future use of stored samples.

You may not qualify if…

• Have an acute illness*, as determined by the site PI or appropriate sub-investigator, within 72 hours prior to each study vaccination.
• An acute illness which is nearly resolved with only minor residual symptoms remaining is allowable if, in the opinion of the site PI or appropriate sub-investigator, the residual symptoms will not interfere with the ability to assess safety parameters as required by the protocol.
• Have any medical disease or condition that, in the opinion of the site PI or appropriate sub-investigator, is a contraindication to study participation*.
• Including acute or chronic medical disease or condition, defined as persisting for at least 90 days, that would place the subject at an unacceptable risk of injury, render the subject unable to meet the requirements of the protocol, or may interfere with the evaluation of responses or the subject's successful completion of this study.
• Have immunosuppression as a result of an underlying illness or treatment, or use of anticancer chemotherapy or radiation therapy (cytotoxic) within 3 years prior to study vaccination.
• Have known active neoplastic disease or a history of any hematologic malignancy. Non-melanoma skin cancers that are not active are permitted.
• Have known HIV, hepatitis B, or hepatitis C infection.
• Have a history of severe reactions following previous immunization with licensed or unlicensed influenza vaccines.
• History of anatomic disorder of the nares or nasopharynx (Deviated septum is allowed).
• History of chronic sinus infections.
• Have a history of Guillain-Barre Syndrome.
• Have a history of alcohol or drug abuse prior to study vaccination.
• Have any diagnosis, current or past, of schizophrenia, bipolar disease, or other psychiatric diagnosis that may interfere with subject compliance or safety evaluations.
• Have been hospitalized for psychiatric illness, history of suicide attempt, or confinement for danger to self or others prior to study vaccination.
• Have taken oral and/or nasal corticosteroids of any dose within 30 days prior to each study vaccination or plan to take in the 30 days following the first study vaccination.
• Have taken high-dose*,** inhaled corticosteroids within 30 days (prior to study vaccination).
• High-dose defined as per age as using inhaled high dose per reference chart.
• *https://www.nhlbi.nih.gov/files/docs/guidelines/asthma_org.pdf.
• Use of aspirin or salicylate-containing products 30 days prior to the first vaccination.
• Recurring or active wheezing or diagnosis of asthma, or history of significant wheezing*.
• Medically significant wheezing: defined as wheezing on physical exam plus sign of respiratory distress (tachypnea, retractions, or dyspnea), hypoxemia (O2 saturation < 95%), or new bronchodilator prescription, or use of daily bronchodilator therapy (not on an "as needed" basis).
• Received any licensed live or inactivated vaccine within 30 days prior to or plan to receive any licensed live or inactivated vaccine within 30 days after each study vaccination.
• Received any influenza vaccine (inactivated or live) within 6 months prior to the first study vaccination and until the end of the study.
• Received immunoglobulin or other blood products within 6 months prior to study vaccination.
• Received an experimental agent* within 30 days prior to the first study vaccination, or expects to receive an experimental agent** during the 12-month trial-reporting period.

Where it is running

• Saint Louis University - Center for Vaccine Development — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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