ClinicalTrials.gg
Not yet recruitingNCT07703514Updated Nov 6, 2026

Safety and Immunogenicity of Chimeric Hemagglutinin mRNA Vaccine Candidates

A Phase 1 interventional study of cH15/3 and cH4/3 in Influenza, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 59 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Phase 1, Interventional, and Prevention

Updated Oct 23, 2026Start date movedGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 59 Years
Sex
All
01

Study summary

This is a Phase 1, randomized, controlled, dose-ranging clinical trial to assess the safety and immunogenicity of novel influenza A Group 1 and influenza A Group 2 mRNA chimeric hemagglutinin (HA) vaccine candidates given as intramuscular injections alone and in combination. A total of 60 healthy men and non-pregnant, non-breastfeeding women aged 18 through 59 years will be enrolled in one of 6 study arms. The 6 arms will consist of: 1) Sequential influenza A Group 1 mRNA chimeric hemagglutinin: cH8/1 (25 µg) followed by cH5/1 (25 µg), 2) Sequential influenza A Group 2 mRNA chimeric hemagglutinin: cH15/3 (25 µg) followed by cH4/3 (25 µg), 3) Sequential combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (25 µg) followed by cH5/1 + cH4/3 (25 µg), 4) A single dose of combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (50 µg) followed by placebo, 5) A single dose of combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH5/1 + cH4/3 (50 µg) followed by placebo, 6) Sequential combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (50 µg) followed by cH5/1 + cH4/3 (50 µg). The primary objectives are to evaluate safety and immunogenicity: 1) To assess the safety and reactogenicity of one or two doses of monovalent or bivalent Group 1 and 2 study products and 2) To describe the Group 1 and 2 anti-HA stalk IgG antibody responses of one or two doses of monovalent or bivalent Group 1 and 2 study products by ELISA.

Read the detailed description

This is a Phase 1, randomized, controlled, dose-ranging clinical trial to assess the safety and immunogenicity of novel influenza A Group 1 and influenza A Group 2 mRNA chimeric hemagglutinin (HA) vaccine candidates given as intramuscular injections alone and in combination. A total of 60 healthy men and non-pregnant, non-breastfeeding women aged 18 through 59 years will be enrolled in one of 6 study arms. The 6 arms will consist of: 1) Sequential influenza A Group 1 mRNA chimeric hemagglutinin: cH8/1 (25 µg) followed by cH5/1 (25 µg), 2) Sequential influenza A Group 2 mRNA chimeric hemagglutinin: cH15/3 (25 µg) followed by cH4/3 (25 µg), 3) Sequential combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (25 µg) followed by cH5/1 + cH4/3 (25 µg), 4) A single dose of combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (50 µg) followed by placebo, 5) A single dose of combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH5/1 + cH4/3 (50 µg) followed by placebo, 6) Sequential combined influenza A Group 1 and Group 2 mRNA chimeric hemagglutinin: cH8/1 + cH15/3 (50 µg) followed by cH5/1 + cH4/3 (50 µg). The primary objectives are to evaluate safety and immunogenicity: 1) To assess the safety and reactogenicity of one or two doses of monovalent or bivalent Group 1 and 2 study products and 2) To describe the Group 1 and 2 anti-HA stalk IgG antibody responses of one or two doses of monovalent or bivalent Group 1 and 2 study products by ELISA. The secondary objective is to describe the Group 1 and Group 2 anti-hemagglutinin stalk Immunoglobulin G (IgG) antibody response of one or two doses of monovalent or bivalent Group 1 and 2 study products by ELISA at a later timepoints.

02

Conditions studied

  • Influenza

Browse trials for

Keywords

  • cH15/3 (WA79/HK14)
  • cH4/3 (CZ56/HK14)
  • cH5/1 (VN04/CA09)
  • cH8/1 (SW02/CA09)
  • Chimeric Hemagglutinin
  • Double Blinded
  • Flu-CHAMPs
  • Healthy adults
  • Immunogenicity
  • Influenza
  • Influenza A
  • mRNA
  • Phase 1
  • Placebo
  • Randomized
  • Safety
  • Vaccine
03

In context

Influenza, Human

2,356 studies on the registry are indexed under Influenza, Human; 184 are open to participants now.

This study's planned enrollment of 60 is below the median of 227 across 1,957 interventional studies indexed under Influenza, Human.

Browse Influenza, Human studies →

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID) is the lead sponsor of 2,446 studies on the registry; 179 are open to participants now.

Of its 405 completed or terminated interventional studies of FDA-regulated products, 302 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 59 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Provision of signed and dated form before the initiation of any study procedures.
  2. Stated willingness to comply with all study procedures and availability for the duration of the study.
  3. Non-pregnant healthy adults, aged 18 to 59 years of age, inclusive, at the time of enrollment.
  4. In good general health as evidenced by medical history or diagnosed with stable chronic medical or psychiatric diagnoses or conditions.*

    *As determined by medical history, medications use, and physical examination to evaluate ongoing chronic medical or psychiatric diagnoses or conditions, defined as those that have been present for at least 90 days, which would not affect the assessment of the safety of participants or the immunogenicity of study products. These medical diagnoses or conditions should be stable for the last 60 days (no hospitalizations, emergency room [ER] or urgent care for the condition [excluding musculoskeletal conditions], or invasive medical procedure and no adverse symptoms that need medical intervention such as medication change/supplemental oxygen). This includes no change in chronic prescription medication or dose as a result of new symptoms or deterioration of the condition or disease being treated in the 30 days prior to enrollment. Any prescription change that is due to a 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. Participants may be on chronic or as-needed (prn) medications if, in the opinion of the site PI or appropriate sub-investigator, they pose no additional risk to participant safety or assessment of reactogenicity and immunogenicity, and do not indicate a worsening or treatment of continued symptoms of medical diagnosis or condition. Note: Low-dose topical as outlined in the Exclusion Criteria as well as herbals, vitamins, and supplements are permitted.

  5. Oral temperature is less than 100.4 degrees Fahrenheit*.

    *Inclusion requirement at enrollment and prior to study product administration.

  6. Heart rate (HR) is 55 to 100 beats per minute, inclusive*. *Screening heart rate values in the normal range or with grade 1 abnormalities deemed not by the site PI or designated clinician licensed to make medical diagnoses and listed on Form FDA 1572 are considered acceptable.
  7. Systolic blood pressure is 90 to 140 mmHg, inclusive*.

    *Screening systolic blood pressure values in the normal range or with grade 1 abnormalities deemed not clinically significant by the site PI or designated clinician licensed to make medical diagnoses and listed on Form FDA 1572 are considered acceptable.

  8. Diastolic blood pressure is 55 to 90 mmHg, inclusive*. *Screening diastolic blood pressure values in the normal range or with grade 1 abnormalities deemed not clinically significant by the site PI or designated clinician licensed to make medical diagnoses and listed on Form FDA 1572 are considered acceptable.
  9. between 18 kilograms/square meter (kg/m\^2) (inclusive) and \<35 kg/m\^2 at screening
  10. Females of * must agree to true abstinence** or use at least 1 acceptable primary form of ***,****

    • Not of childbearing potential - females (defined as having a history of amenorrhea for at least one year) or a documented status as being surgically sterile (hysterectomy, bilateral oophorectomy, salpingectomy, or Essure® placement with history of documented radiological confirmation test at least 90 days after the procedure).

      **True abstinence is 100% of the time, no sexual intercourse (male's penis enters the female's vagina). (Periodic abstinence [e.g., calendar, ovulation, symptothermal, post-ovulation methods] and withdrawal are not acceptable methods of contraception).

      ***Acceptable forms of primary contraception include monogamous relationship with a vasectomized partner who has been vasectomized for 180 days or more prior to the subject receiving the study product, tubal ligation, intrauterine devices, birth control pills, and injectable/implantable/insertable hormonal birth control products

      ****Must use at least one acceptable primary form of contraception for at least 30 days before screening and agreement to use such a method during study participation and for an additional 30 days after the end of last study product administration.

  11. Females of must have a negative serum pregnancy test at screening and a negative urine pregnancy test within 24 hours before the study product administration.
  12. Must agree to have samples collected for secondary research.

Exclusion criteria

Exclusion Criteria:

  1. A history of any medical disease or condition that, in the opinion of the site PI or appropriate sub-investigator, is a to study participation*.

    *Including acute, subacute, intermittent, or chronic medical disease or condition that would place the participant at an unacceptable risk of injury, render the participant unable to meet the requirements of the protocol, or may interfere with the evaluation of responses or the participant's successful completion of this trial.

  2. A history of any known or suspected condition, acquired or congenital, or conditions as determined by history and/or physical examination.
  3. A history of known active or recently active (12 months) neoplastic disease or a history of any hematologic . (Non-melanoma, treated, skin cancers are permitted.)
  4. A history of myocarditis or pericarditis.
  5. A history of Guillain-Barré Syndrome.
  6. Receipt of anticancer chemotherapy or radiation therapy (cytotoxic) within 3 years before study product administration.
  7. Current pregnancy or breastfeeding.
  8. Known allergic reactions to components of the products or seasonal influenza vaccine.
  9. Febrile illness or other acute illness* within 72 hours before the first study product administration.

    *An acute illness that 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.

  10. Receipt of another experimental agent* or other intervention within 60 days before the first study product administration**.

    *Including vaccine, drug, biologic, device, blood product, or medication.

    **Other than from participation in this trial

  11. Any condition that, in the judgment of the investigator, precludes participation because it could affect participant safety.
  12. Has a positive test result for surface antigen, virus antibody*, or type 1 or 2 antibodies at screening.

    *Persons testing positive for hepatitis C virus antibody with a history of treatment and a negative HCV viral load may be acceptable in the opinion of the PI or appropriate Sub-Investigator.

  13. Currently enrolled in or plans to participate in another clinical trial with an investigational agent*that will be received during the study-reporting period**.

    *Including licensed or unlicensed vaccine, drug, biologic, device, blood product, or medication.

    **Approximately 10 months after the first study product administration.

  14. Has a history of or severe allergic reaction* to any previous licensed or unlicensed influenza, mRNA, or LNP-containing vaccines.

    *For example, anaphylaxis, generalized urticaria, angioedema, or other significant reactions.

  15. Chronic use (more than 14 continuous days) of any medications that may be associated with impaired immune responsiveness*.

    *Including, but not limited to, systemic exceeding 10 mg/day of prednisone equivalent, allergy injections, immunoglobulin, interferon, immunomodulators, cytotoxic drugs, or other similar or toxic drugs during the preceding 6-month period before study product administration (Day 1). The use of low-dose topical, ophthalmic, inhaled, and intranasal steroid preparations will be permitted.

  16. Anticipating the need for immunosuppressive treatment within the next 6 months.
  17. Received immunoglobulins and/or any blood or blood products (except Rho D immunoglobulin) within the 4 months before the first study product administration.
  18. Plans to donate blood or blood products from screening through 90 days after dosing.
  19. Has any blood dyscrasias or significant disorder of coagulation.
  20. Has any chronic liver disease, including fatty liver.
  21. Has a history of alcohol abuse or other recreational drug (excluding cannabis) use within 6 months before the first study product administration.
  22. Has any abnormality or permanent body art (e.g., tattoo) that would interfere with the ability to observe local reactions at the injection site.
  23. Received or plans to receive a licensed, within 4 weeks before first study product administration through 4 weeks after last study product administration.
  24. Received or plans to receive a licensed, inactivated vaccine within 2 weeks before first study product administration through 2 weeks after last study product administration.
  25. Received or plans to receive a seasonal influenza vaccine within 90 days before first study product administration through 90 days after last study product administration.
  26. Have a known history of confirmed influenza virus infection within the past 90 days.
  27. Have screening clinical laboratory examinations of grade 1 or above*.

    *Grade 1 criteria for clinical laboratory (WBC count, , count, creatinine, , total ) may be acceptable if deemed not by the site principal investigator (PI) or the study clinician listed on the delegation log.

  28. Has had a positive SARS-CoV-2 test (home or laboratory-based) within 7 days before the screening visit or during the period between screening and enrollment visits.
Terms in these criteria, in plain language(22)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Reproductive potential

Able to have children. For women this usually means from the first period until menopause, unless permanently unable to through surgery; for men, unless permanently sterile. Read who the line is about — participants, women, men, or their partners.

Criteria about it usually ask for contraception during the study and for a time after it.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Cohort 1, Arm1

    Healthy adults will receive 2 monovalent dose intramuscular injections. cH8/1 (25ug) chimeric Hemagglutinin (HA) is the first dose given on Day 1, followed by a second dose administered 57 days later with cH5 /1(25 ug). N = 10

    Biological: cH5/1N1 · Biological: cH8/1N1

  • Experimental
    Cohort 1, Arm2

    Healthy adults will receive 2 monovalent dose intramuscular injections. cH15/3 (25ug) chimeric HA is the first dose given on Day 1, followed by a second dose of cH4/3 (25ug), administered 57 days later. N = 10.

    Biological: cH15/3 · Biological: cH4/3

  • Experimental
    Cohort 1, Arm3

    Healthy adults will receive 2 low dose bivalent intramuscular injections. cH8/1(12.5ug) + cH15/3 (12.5ug) chimeric HA is the first dose given on Day 1, followed by a second dose of cH5/1 (12.5ug) + cH4/3(12.5 ug) administered 57 days later. N = 10.

    Biological: cH15/3 · Biological: cH4/3 · Biological: cH5/1N1 · Biological: cH8/1N1

  • Experimental
    Cohort 2, Arm4

    Healthy adults will receive a single high dose bivalent combination intramuscular injection along with a placebo dose. cH8/1(25ug) + cH15/3(25ug) will be administered on Day 1, followed by a placebo dose 57 days later. N = 10.

    Biological: cH15/3 · Biological: cH8/1N1 · Drug: Saline

  • Experimental
    Cohort 2, Arm5

    Healthy adults will receive a single high dose bivalent combination intramuscular injection along with a placebo dose. cH5/1(25ug) + cH4/3(25ug) will be administered on Day 1, followed by a placebo dose 57 days later. N = 10.

    Biological: cH4/3 · Biological: cH5/1N1 · Drug: Saline

  • Experimental
    Cohort 2, Arm6

    Healthy adults will receive 2 high dose bivalent intramuscular injections. cH8/1(25ug) + cH15/3 (25ug) is the first dose given on Day 1, followed by the second dose of cH5/1(25 ug) + cH4/3 (25 ug) administered 57 days later. N = 10.

    Biological: cH15/3 · Biological: cH4/3 · Biological: cH5/1N1 · Biological: cH8/1N1

Interventions

  • BiologicalcH15/3

    The cH15/3 RNA study product encodes for a novel chimeric hemagglutinin comprised of an H15 HA head domain derived from influenza A/wedge-tailed shearwater/Western Australia/2576/1979 (H15N9) and the conserved stem domain derived from influenza A/Hong Kong/2014 (H3N2) (GenBank: OQ349633). The cH15/3 RNA is encapsulated in LNPs for delivery. The LNP is comprised of 4 lipid components: ionizable lipid (ALC-0315), distearoylphosphatidylcholine (DSPC), cholesterol (non-animal derived), and PEG lipid (ALC-0159).

  • BiologicalcH4/3

    The cH4/3 RNA encodes a novel chimeric hemagglutinin comprised of an H4 head domain from A/duck/Czechoslovakia/1956 (H4N6) and a conserved stem domain from A/Hong Kong/2014 (H3N2) (GenBank: OQ349617), delivered via lipid nanoparticles (LNPs) containing ionizable lipid (ALC-0315), distearoylphosphatidylcholine (DSPC), cholesterol (non-animal derived), and PEG lipid (ALC-0159).

  • BiologicalcH5/1N1

    cH5/1N1 is a H1N1 influenza vaccine: egg grown split inactivated influenza virus vaccines containing chimeric hemagglutinins (HAs). The chimeric viruses contain the globular heads of exotic viruses- and the HA stem domain and neuraminidase protein from currently circulating seasonal H1N1.

  • BiologicalcH8/1N1

    cH8/1N1 is a H1N1 influenza vaccine: egg grown split inactivated influenza virus vaccines containing chimeric hemagglutinins (HAs). The chimeric viruses contain the globular heads of exotic viruses- and the HA stem domain and neuraminidase protein from currently circulating seasonal H1N1.

  • DrugSaline

    Sodium chloride solution.

06

What researchers measure

Primary outcomes

  1. Geometric mean fold rise (GMFR) from baseline in HA-stalk specific titers by ELISA

    Time frame: Day 1 through Day 85

  2. Geometric mean titer (GMT) by ELISA

    Time frame: Day 1 Through Day 85

  3. Number and percentage of participants with greater than or equal to a 2-, 4-, and 10-fold rise from baseline in Hemagglutinin (HA)-stalk specific titers by ELISA

    Time frame: Day1 through Day 85

  4. Occurrence of Adverse Events of Special Interest (AESIs)

    Time frame: Day 1 through Day 240

  5. Occurrence of Guillain-Barre Syndrome (GBS)

    Time frame: Through Day 240

  6. Occurrence of hematological or biochemical laboratory adverse events

    Time frame: Day 8 through Day 64

  7. Occurrence of laboratory confirmed influenza A infection

    Time frame: Through Day 240

  8. Occurrence of Medically-Attended Adverse Events (MAAEs)

    Time frame: Through Day 240

  9. Occurrence of New-Onset Chronic Medical Conditions (NOCMCs)

    Time frame: Through Day 240

  10. Occurrence of Serious Adverse Events (SAEs)

    Time frame: Through Day 240

  11. Occurrence of solicited local adverse events (AEs)

    Time frame: Day 1 through Day 64

  12. Occurrence of solicited systemic adverse events (AEs)

    Time frame: Day 1 through Day 64

  13. Occurrence of unsolicited adverse events (AEs)

    Time frame: Day 1 through Day 85

Secondary outcomes

  1. Geometric mean fold-rise (GMFR) from baseline in Hemagglutinin (HA) stalk specific titers by ELISA

    Time frame: Day 240

  2. Hemagglutinin (HA)-stalk specific geometric mean titer (GMT) by ELISA

    Time frame: Day 240

  3. Number and percentage of participants with greater than or equal to a 2-, 4-, and 10-fold rise from baseline in Hemagglutinin (HA) -stalk specific titers by ELISA

    Time frame: Day 240

07

Study locations

1 site
  • University of Maryland, School of Medicine, Center for Vaccine Development and Global Health
    Baltimore, Maryland 21201-1509, United States
08

Updates

4 registry updates since Sep 25, 2026
Start date
Aug 28, 2026→Oct 9, 2026
moved 2 times, Oct 9, 2026 – Oct 23, 2026
Show all 4 updates
  1. Oct 30, 2026
    Minor edits only
    + 1 other change: verification date
  2. Oct 23, 2026
    Start date Sep 18, 2026→Oct 9, 2026
    + 1 other change: verification date
  3. Oct 16, 2026
    Minor edits only
    + 1 other change: verification date
  4. Oct 9, 2026
    Start date Aug 28, 2026→Sep 18, 2026
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07703514
Responsible party
Sponsor
First posted
Jul 14, 2026
Start date
Oct 9, 2026 (estimated)
Primary completion
Apr 12, 2027 (estimated)
Completion
Apr 12, 2027 (estimated)
Last update
Nov 6, 2026

Study contacts

Meagan Deming
Contact
mdeming@som.umaryland.edu
14107068333

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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