Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

NCT ID: NCT02669121

Last Updated: 2021-06-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 4748 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-06-14
• Study Completion Date: 2018-06-16

Brief Summary

The purpose of this study is to evaluate the efficacy of the Norovirus (NoV) GI.1/GII.4 bivalent virus-like particle vaccine against moderate or severe acute gastroenteritis (AGE) due to genotype-specific (GI.1 and GII.4) NoV strains.

Detailed Description

The vaccine being tested in this study is called NoV GI.1/GII.4 bivalent VLP vaccine adjuvanted with aluminum hydroxide. The norovirus vaccine is being tested to prevent AGE due to genotype-specific (GI.1 and GII.4) norovirus strains in healthy participants recruited from a US military training installation. This study will look at the illness rate of AGE occurring > 7 days after dosing due to genotype-specific (GI.1 or GII.4) NoV strains represented in the vaccine.

The study will enroll between 2800 and 8700 patients. Participants will be randomly assigned (by chance, like flipping a coin) to one of the two treatment groups-which will remain undisclosed to the participant and study doctor during the study (unless there is an urgent medical need):

• Norovirus GI.1/GII.4 Bivalent VLP Vaccine
• Placebo (dummy inactive solution) - this is a liquid that looks similar to the study drug but has no active ingredient

All participants will receive one dose of study medication on Day 1 administered via intramuscular injection.

This multi-center trial will be conducted in the United States at select military locations. The overall time to participate in this study is up to 45 days for participants in the navy 53 days for participants in the Air Force, and 72 days for participants in the marines. Participants will make multiple visits to the clinic, including a final visit on the last day of study participation (Day 45, 53 or 72) for a follow-up assessment.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

NoV placebo-matching 0.5 mL solution for injection, intramuscularly (IM), once, on Day 1.

Group Type: PLACEBO_COMPARATOR

NoV Placebo-matching Saline

Intervention Type: BIOLOGICAL

NoV placebo-matching saline (0.9% sodium chloride).

NoV GI.1/GII.4 Bivalent VLP Vaccine

NoV GI.1/GII.4 bivalent virus-like particle (VLP) vaccine, 0.5 mL injection, intramuscularly (IM), once, on Day 1.

Group Type: EXPERIMENTAL

NoV GI.1/GII.4 Bivalent VLP Vaccine

Intervention Type: BIOLOGICAL

NoV bivalent VLP vaccine, adjuvanted with 500 µg aluminum as Al(OH)3.

Interventions

NoV Placebo-matching Saline

NoV placebo-matching saline (0.9% sodium chloride).

Intervention Type: BIOLOGICAL

NoV GI.1/GII.4 Bivalent VLP Vaccine

NoV bivalent VLP vaccine, adjuvanted with 500 µg aluminum as Al(OH)3.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Participant signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any trial procedures after the nature of the trial has been explained according to local regulatory requirements.

2. Male or female participants, 18 to 49 years of age.

3. Is in good health at the time of entry into the trial as determined by medical history and the clinical judgment of the investigator.

4. Can comply with trial procedures and are available for the duration of follow-up.

Exclusion Criteria

1. Pregnancy.

2. Has known hypersensitivity to any of the Norovirus (NoV) GI.1/GII.4 bivalent virus-like particle (VLP) vaccine components (including excipients).

3. Has known hypersensitivity or allergy to any of the licensed required concomitant vaccine components to be administered (including excipients of these vaccines).

4. Has any condition or circumstance that the investigator determines would interfere with trial evaluation or interpretation.

5. Has known or suspected impairment or alteration of immune function.

6. Has a history of acute gastroenteritis (AGE) within 14 days of enrollment.

7. Has a history of body temperature of 38.0°C (100.4°F) or higher within 3 days of intended trial vaccination.

8. Has received blood, blood products, and/or plasma derivatives or any parenteral immunoglobulin antibody preparation in the past 3 months.

9. Immunosuppressive therapy within 3 months or systemic (e.g., oral or parenteral) corticosteroid treatment within 60 days prior to investigational trial dose administration.

10. Is participating in any clinical trial with another investigational product 30 days prior to the first trial visit or intending to participate in another clinical trial at any time during the conduct of this trial.

11. Participants who are first-degree relatives of individuals involved in the conduct of the trial.

12. Has any history of progressive or severe neurologic disorder, seizure disorder or neuro-inflammatory disease (e.g. Guillain-Barré syndrome).

13. Has history or any illness that, in the opinion of the investigator, might interfere with the results of the trial or pose additional risk to the participants due to participation in the trial.

14. Has received any other vaccines within 14 days (for inactivated vaccines) or 28 days (for live vaccines) prior to enrollment in this trial with the exception of routine immunizations as per Military Procedures.

15. If female of childbearing potential, sexually active, and has not used any of the "acceptable contraceptive methods" for at least 2 months prior to trial entry:

1. Of childbearing potential is defined as status post onset of menarche and not meeting any of the following conditions: menopausal for at least 2 years, status after bilateral tubal ligation for at least 1 year, status after bilateral oophorectomy, or status after hysterectomy.

2. Acceptable birth control methods are defined as one or more of the following:

• Hormonal contraceptive (such as oral, injection, transdermal patch, implant, cervical ring).
• Barrier (condom with spermicide or diaphragm with spermicide) each and every time during intercourse.
• Intrauterine device (IUD).
• Monogamous relationship with vasectomized partner. Partner must have been vasectomized for at least six months prior to the participants' trial entry.

16. If female of childbearing potential and sexually active, refusal to use an "acceptable contraceptive method" from Day 1 through 6 months after the last dose of trial vaccine. In addition, they must be advised not to donate ova during this period.

17. Has any positive or indeterminate pregnancy test.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 49 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Study Director

Role: STUDY_DIRECTOR

Takeda

Locations

Great Lakes Naval Station

Great Lakes, Illinois, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

U1111-1175-9077

Identifier Type: REGISTRY

Identifier Source: secondary_id

NOR-211

Identifier Type: -

Identifier Source: org_study_id