A Study to Describe the Safety and Immunogenicity of a Respiratory Syncytial Virus Vaccine IN006 in Healthy Adult Aged 18 Years and Above

NCT ID: NCT06645665

Last Updated: 2024-11-21

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 240 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-11-11
• Study Completion Date: 2027-04-30

Brief Summary

The study will evaluate the safety, tolerability, and immunogenicity of 3 dose levels of IN006 in healthy adults aged 18 Years and Above; of a revaccination of IN006 given approximately 12 months after the initial vaccination in older adults (aged ≥60 years).

Conditions

Respiratory Syncytial Virus Infections

Study Design

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

Study Groups

Cohort 1: Dose A in Younger Adults

Single injection of Dose A of IN006 or matching-placebo on Day 0

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Cohort 2: Dose B in Younger Adults

Single injection of Dose B of IN006 or matching-placebo on Day 0.

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Cohort 3: Dose C in Younger Adults

Single injection of Dose C of IN006 or matching-placebo on Day 0.

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Cohort 4: Dose A in Older Adults

One injection of either Dose A of IN006 or matching-placebo on Day 0. Participants who initially assigned to receive IN006 on Day 0 will be further randomized to receive a second injection of either IN006 or matching-placebo approximately 12 months later.

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Cohort 5: Dose B in Older Adults

One injection of either Dose B of IN006 or matching-placebo on Day 0. Participants who initially assigned to receive IN006 on Day 0 will be further randomized to receive a second injection of either IN006 or matching-placebo approximately 12 months later.

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Cohort 6: Dose C in Older Adults

One injection of either Dose C of IN006 or matching-placebo on Day 0. Participants who initially assigned to receive IN006 on Day 0 will be further randomized to receive a second injection of either IN006 or matching-placebo approximately 12 months later.

Group Type: EXPERIMENTAL

Bivalent RSV Vaccine (IN006)

Intervention Type: BIOLOGICAL

Formulation for injection

Placebo

Intervention Type: BIOLOGICAL

0.9% sodium chloride (normal saline) injection

Interventions

Bivalent RSV Vaccine (IN006)

Formulation for injection

Intervention Type: BIOLOGICAL

Placebo

0.9% sodium chloride (normal saline) injection

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. Healthy people aged 18-59 (Part 1) or ≥60 (Part 2), male or female.

2. Body mass index (BMI) in the range of 18 to 29 kg/m^2.

3. Laboratory tests, 12-lead electrocardiogram, chest radiograph, vital signs and physical examination results are normal during the screening period, or abnormal results assessed by the investigator had no clinical significance; Subjects ≥60 years old with stable medical conditions, whose risk was considered controllable by the investigator, could also be enrolled.

4. Women of childbearing age took effective contraception within 2 weeks before joining the study, and the pregnancy test results before vaccination are negative. All male and female subjects of reproductive age voluntarily agree to use effective contraception from the signing of informed consent until 6 months after vaccination.

Exclusion Criteria

1. The results of vital signs show: for subjects with no history of hypertension or hypotension, systolic blood pressure ≥140mmHg or < 90mmHg, and/or diastolic blood pressure ≥90mmHg or < 50mmHg; for subject with a history of hypertension not appropriately controlled via pharmaceutical treatment, systolic blood pressure ≥140mmHg or diastolic blood pressure ≥90mmHg in those aged 40-59, and systolic blood pressure ≥150mmHg or diastolic blood pressure ≥90mmHg in those aged 60 and above. Pulse rate > 100 beats/min or < 50 beats/min; Ear temperature/oral temperature > 37.5°C (or axillary temperature > 37.0°C).

2. Laboratory tests, 12-lead electrocardiogram, chest radiography (orthographic) and physical examination results: For subjects aged 18-59 years old, abnormal results judged to be clinically significant by the investigator, or for subjects ≥60 years old, abnormal results judged to be > Grade 1 criteria by the investigator; For laboratory tests, a retest may be conducted at the discretion of investigators to determine subjects eligibility.

3. Those with tattoos, scars and ecchymosis at the injection site.

4. Known allergy to the experimental vaccine or its excipient, or history of severe allergy to other vaccines, foods, drugs, etc.

5. The subject has received any previous investigational or marketed RSV vaccine, or has received investigational or marketed RSV prophylactic monoclonal antibody within the last 6 months.

6. Received inactivated, subunit, or recombinant influenza vaccine within 14 days prior to enrollment, or received any live vaccine, nucleic acid vaccine, or adenovirus vector vaccine within 28 days prior to enrollment; Or plan to receive other vaccines within 28 days of vaccination.

7. Used antipyretic, analgesic or anti-allergic drugs within 3 days before enrollment.

8. Have received blood or blood-related products (including immunoglobulins) within 3 months prior to enrollment, or had planned to use them during the study period.

9. People with the following diseases:

• A history of acute respiratory infection within 2 weeks of vaccination or a history of confirmed RSV-associated respiratory infection within 3 months prior to vaccination;
• History of congenital or acquired immune deficiency or autoimmune disease, or long-term use (continuous use > 14 days) of corticosteroids (dose ≥20mg/ day prednisone or equivalent dose) or other immunosuppressants within the past 6 months;
• people who are known to have been diagnosed with or currently have infectious diseases (including hepatitis B, hepatitis C, syphilis, and acquired immunodeficiency syndrome), or whose test positive for any of the hepatitis B surface antigens, hepatitis C antibodies, treponema pallidum antibodies, or human immunodeficiency virus antibodies;
• A history or family history of neurological disease (convulsions, seizures, etc.); History or family history of mental illness;
• Asplenia, or functional asplenia;
• A history of myocarditis, pericarditis, or idiopathic cardiomyopathy, or any condition that increases the risk of myocarditis or pericarditis;
• History of inflammatory demyelinating neuropathy such as Guillain-Barre syndrome;
• Severe cardiovascular diseases, diabetes, blood and lymphatic system diseases, immune system diseases, liver and kidney diseases, respiratory diseases, metabolic and skeletal diseases, or malignant tumors (excluding stable chronic medical history, such as diabetes, hypertension, etc.);
• Contraindications to intramuscular injection and blood drawing;
• A history of tuberculosis (TB) or a positive T-cell test for TB infection (T-SPOT).

10. Had a history of major surgery within 3 months prior to vaccination or planned surgery during the trial.

11. Abuser of Drug or alcohol in the year prior to screening, which the investigator believes that it may impact on subjects' safety assessment or compliance.

12. Women of childbearing age who are breastfeeding, pregnant, have positive pregnancy test results or plan to become pregnant within 6 months after participating in the study.

13. Those who have received a vaccine or drug involving lipid nanoparticles (LNP) within 1 year, are participating in other RSV-related clinical trials, and are in or plan to participate in other clinical trials during the study period.

14. The investigator assesses that the subject has any disease or condition that would place the subject at an unacceptable risk; The subject is unable to meet protocol requirements; Conditions that interfere with the assessment of vaccine response.

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

Sponsors

Shenzhen Shenxin Biotechnology Co., Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Huashan Hospital Affiliated to Fudan University

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Anning First People's Hospital

Kunming, Yunnan, China

Site Status: RECRUITING

Countries

China

Central Contacts

Clinical Development Innorna

Role: CONTACT

cd@innorna.com

+86-755-86532375

Other Identifiers

IN006002

Identifier Type: -

Identifier Source: org_study_id