Safety and Immunogenicity of SYS6017 in Healthy Participants Aged 40 Years or More

CSPC Megalith Biopharmaceutical Co.,Ltd.

Status and phase: Not yet enrolling; Phase 1

Conditions: Herpes Zoster

Treatments: Other: Placebo; Biological: A zoster mRNA vaccine SYS6017

Study type: Interventional

Funder types: Industry

Identifiers

NCT06954818

SYS6017-001

Details and patient eligibility

About

Herpes zoster is caused by the reactivation of latent varicella-zoster virus (VZV) which stays in latency after its primary infection. Immunosenescence contributes significantly to elevating morbidity associated with aging. Vaccination plays a key role in reducing the disease burden of zoster and the associated complications. This randomized, observer-blind, placebo-controlled, adaptive phase 1 trial aims to evaluate the safety and immunogenicity of an investigational zoster mRNA vaccine in healthy participants aged 40 years or more.

Enrollment: 200 estimated patients

Sex: All

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 1. Healthy participants aged 40 years or more;
• 2. Be able to understand the study procedures and comply with the requirements of the protocol for the scheduled visits, voluntarily consent to participate in the study and sign the informed consent form (ICF);
• 3. Being in good health at the discretion of investigators based on medical history inquiry, physical examination, laboratory test and electrocardiograph examination;
• 4. For female participants of childbearing potential: no sexual activity or used effective contraceptive methods within one menstrual cycle before enrollment; no pregnancy plans and agree to used effective contraceptive methods with 8 months after enrollment.

Exclusion criteria

• 1. History of zoster;
• 2. History of vaccination with varicella vaccine or zoster vaccine (including investigational vaccine);
• 3. Axillary temperature ≥ 37.1℃ on the day of enrollment or within 24 h before enrollment;
• 4. Have abnormal test or examination result that is of Grade 1 (inclusive) or more in accordance with the Guidelines for Adverse Event Grading Standards for Clinical Trials of Preventive Vaccines (2019) issued by China National Medical Products Administration or other applicable adverse event grading standards referred in the protocol;
• 5. History of allergy to any component of the investigational vaccine, or history of severe allergic reaction (including but not limited to anaphylaxis, allergic laryngeal edema, Henoch-Schonlein purpura, thrombocytopenia purpura or Arthus reaction) to vaccines or medicines;
• 6. History of myocarditis, pericarditis, or idiopathic cardiomyopathy, or any condition that would increase the risk of myocarditis or pericarditis;
• 7. History of demyelinating diseases, including but not limited to Guillain-Barré syndrome, multiple sclerosis, ophthalmoneuromyelitis, acute disseminated encephalomyelitis, etc.
• 8. Current epilepsy or convulsion, severe neurological or psychiatric disorders;
• 9. Have contraindications to intramuscular injection, e.g., diagnosed thrombocytopenia, any coagulation disorders, or current treatment with anticoagulants, etc;
• 10. Active malignant tumor, malignant tumor without adequate treatment, malignant tumor with a potential risk of recurrence during the study;
• 11. Active, unstable, severe or uncontrolled cardiovascular and cerebrovascular diseases, thrombotic diseases, blood and lymphatic system diseases, liver and kidney diseases, respiratory diseases, metabolic diseases, musculoskeletal diseases, autoimmune diseases, etc;
• 12. Have diagnosed immunocompromise or immunosuppression, congenital or functional asplenia, or splenectomy;
• 13. Have received immunosuppressants, immunostimulants, or other immunomodulatory medicines (e.g., corticosteroids, ≥ 20 mg/d prednisone or equivalent) for a long time (defined as 14 days or more), within 6 months before enrollment, or planning to receive the aforementioned medicines during the study; inhaled and topical steroids are allowed;
• 14. Have received whole blood, plasma, serum, immunoglobulins, or monoclonal antibodies within 3 months before enrollment, or planning to receive these products during the study;
• 15. Blood donation or blood loss ≥ 450 mL within 1 month before enrollment, or planning to donate blood during the study;
• 16. Have received any other vaccine within 30 days before enrollment, or planning to receive any other vaccine within 30 days after the last dose;
• 17. Currently participating in or planning to participate in other clinical trials during the study;
• 18. For female participant of childbearing potential: having positive urine pregnancy test, being in pregnancy or lactation before enrollment;
• 19. Unable to comply with the study procedures or adhere to the study requirements, or there are other conditions that make the participation in this study inappropriate, as determined by the investigators.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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200 participants in 6 patient groups, including a placebo group

Investigational vaccine of Dosage A

Experimental group

Treatment:

Biological: A zoster mRNA vaccine SYS6017

Investigational vaccine of Dosage B

Experimental group

Treatment:

Biological: A zoster mRNA vaccine SYS6017

Investigational vaccine of Dosage C

Experimental group

Treatment:

Biological: A zoster mRNA vaccine SYS6017

Investigational vaccine of Dosage D

Experimental group

Treatment:

Biological: A zoster mRNA vaccine SYS6017

Investigational vaccine of Dosage E

Experimental group

Treatment:

Biological: A zoster mRNA vaccine SYS6017

Placebo

Placebo Comparator group

Treatment:

Other: Placebo