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Trial - NCT05886790


Column Value
Trial registration number NCT05886790
Full text link
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

First author
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Jianying Huang

Contact
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

znyylcsy@126.com

Registration date
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

2023-06-02

Recruitment status
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Recruiting

Study design
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

RCT

Allocation
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Randomized

Design
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Parallel

Masking
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Open label

Center
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

single-center

Study aim
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Prevention

Inclusion criteria
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

inclusion criteria: volunteers aged 18 and above at the time of screening; volunteers can provide with informed consent and sign informed consent form (icf); have received covid-19 vaccine, and the interval between the last vaccination ≥ 3 months.

Exclusion criteria
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

those with convulsions, epilepsy, encephalopathy and serious neurological diseases (such as transverse myelitis, guillain-barre syndrome, demyelinating disease, etc.) in the past five years; those who are allergic to the active ingredient, any inactive ingredient, or substances used in the production process of the research vaccine, or those who are allergic to the similar vaccines previously; those who have had severe allergic reactions to vaccines in the past (such as acute allergic reactions, angioedema, dyspnea, etc.), and have any previous history of severe allergies to vaccines, foods, drugs, such as: urticaria, anaphylactic shock, skin eczema, allergic dyspnea, angioedema, etc. or a history of asthma; those who have previously suffered from severe heart diseases such as myocarditis and pericarditis; those who have experienced vaccination-related hospitalization or emergency care after previous vaccination; female urine pregnancy test positive or lactating volunteers, volunteers or their partners have not taken effective contraception 2 weeks before screening or have a pregnancy plan within 6 months; fever, axillary body temperature≥ 37.3°c; those with suspected symptoms of covid-19 in the past 3 months (fever, cough, muscle pain, loss of smell or taste, etc.); investigators judge that they have known or suspected concomitant serious diseases with unstable drug control, including: respiratory diseases, tuberculosis, acute infection or active chronic disease, liver and kidney disease, cardiovascular disease (cardiopulmonary failure), hypertension (systolic blood pressure ≥ 160 mmhg, diastolic blood pressure ≥100 mmhg), malignant tumors, infectious or allergic skin diseases; no spleen or functional spleen; thrombocytopenia, bleeding disorders, or other coagulation disorders (which may cause contraindications to intramuscular injection); immunosuppressant therapy, anti-allergic therapy, cytotoxic therapy, inhaled corticosteroids (excluding corticosteroid spray therapy for allergic rhinitis, superficial corticosteroid therapy for acute non-complicated dermatitis) in the past 6 months; suffering from nasal or oral diseases, such as acute rhinitis (sinusitis), allergic rhinitis, mouth ulcers, throat redness and swelling, etc.; have received blood products within 3 months prior to receiving the test vaccine; have received other vaccines or investigational drugs within 1 month prior to receiving the test vaccine; are receiving anti-tuberculosis treatment; those with a history of covid-19 infection in the past 3 months; those who have a positive test result of the novel coronavirus antigen at the time of screening; those with positive hiv infection results at screening; participated in other interventional studies of lipid-containing nanoparticles; according to the judgment of the investigator, due to various medical, psychological, social or other conditions, it is contrary to the trial protocol, or affects the volunteers' signing of informed consent.

Number of arms
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

3

Funding
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Zhongnan Hospital

Inclusion age min
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

18

Inclusion age max
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

100

Countries
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

China

Type of patients
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Healthy volunteers

Severity scale
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

N/A

Total sample size
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

450

primary outcome
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Anti-XBB-specific neutralizing antibody;The incidence of adverse reactions

Notes
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

None

Phase
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

Not reported

Arms
Last imported at : June 4, 2023, 4 a.m.
Source : ClinicalTrials.gov

[{"arm_notes": "", "treatment_id": 2738, "treatment_name": "Ad5-nco5t-ih", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "", "treatment_id": 2739, "treatment_name": "Mbo5", "treatment_type": "Rna based vaccine", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "", "treatment_id": 2066, "treatment_name": "Ad5-ncov-ih", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}]