Clinical Trial of SARS-CoV-2 mRNA Vaccine(LVRNA009) as Heterologous Booster in Islamabad

NCT05428592 | Unknown Phase 3

• 1 other identifier: LVRNA009-Ⅲ-02
• Study Type: interventional
• Target: 1,100
• Locations: 1 country
• Sites: 1

Brief Summary

This study is a randomized, blinded, parallel-controlled phase 3 clinical trial. The study intent to evaluate the immunogenicity and safety of SARS-CoV-2 mRNA Vaccine (LVRNA009) as heterologous booster in participants aged 18 years and older vaccinated 2 doses Inactivated SARS-CoV-2 Vaccine.

Conditions

SARS-CoV-2

Outcome Measures

Primary Outcomes (5)

• Geometric mean titer (GMT) of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  14 days after vaccination for all participants

• Seroconversion Rate (SCR) of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  Seroconversion is defined as: GMT post vaccination≥ 4-fold rise from baseline GMT value

  14 days after vaccination for all participants

• Incidence of each solicited (local and systemic) AE and each unsolicited AE

  AE within 14 days, unsolicited AE within 28 days after vaccination for all participants

• Intensity of each solicited (local and systemic) AE and each unsolicited AE

  AE within 14 days, unsolicited AE within 28 days after vaccination for all participants

• Duration of each solicited (local and systemic) AE and each unsolicited AE

  AE within 14 days, unsolicited AE within 28 days after vaccination for all participants

Secondary Outcomes (13)

• Geometric mean increase (GMI) of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  14 days after vaccination for all participants

• GMT of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  28 days, 3 months, 6 months, and 12 months after vaccination for all participants

• SCR of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  28 days, 3 months, 6 months, and 12 months after vaccination for all participants

• GMI of SARS-CoV-2 (Wild-type strain) VNA (live virus neutralizing assay)

  28 days, 3 months, 6 months, and 12 months after vaccination for all participants

• GMT of SARS-CoV-2 (Wild-type strain) VNA (pseudo-virus neutralizing assay)

  14 days, 28 days, 3 months, 6 months, and 12 months after vaccination for all participants

Other Outcomes (2)

• Cellular immune subgroup: virus antigen-specific IL-2, IL-4, IL-13, IFN-γ cytokine titers (ELISpot)

  7 days, 14 days, and 28 days after vaccination

• Cross-neutralization subgroup: cross-neutralizing ability of VNA (live virus neutralizing assay) against other VOCs of SARS-CoV-2

  14 and 28 days after vaccination

Study Arms (2)

LVRNA009 study group

EXPERIMENTAL

Biological: LVRNA009

CoronaVac® control group

ACTIVE COMPARATOR

Biological: CoronaVac®

Interventions

LVRNA009 BIOLOGICAL

50μg /0.5 mL/Vial/person

LVRNA009 study group

CoronaVac® BIOLOGICAL

0.5 mL/Vial, 0.5mL per human dose containing 600SU of inactivated SARS-CoV-2 antigen

CoronaVac® control group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adults aged 18 years and older.
• Understand the contents of the ICF and voluntarily sign it (If the participant is unable to sign the ICF on his/her own due to illiteracy, an impartial witness is needed).
• Participants who are willing and able to comply with study requirements, including all scheduled visits, vaccinations, laboratory tests, and other study procedures.
• Female participants of childbearing potential or partners of male participants: voluntarily agree to use effective contraception with their partners 14 days prior to the vaccination and must agree to continue such precautions during the study until 3 months after vaccination. \[Effective contraception includes oral contraceptives, injectable or implantable contraception, extended-release topical contraceptives, hormonal patches, intrauterine devices (IUDs), sterilization, abstinence, condoms (for males), diaphragms, cervical caps, etc.\].
• For female participants: without childbearing potential (amenorrhea for at least 1 year or documented surgical sterilization) or have used effective contraception with a negative pregnancy test before vaccination in this study.
• Axillary temperature \<37.3°C/99.1°F at screening visit and 72 hours prior to vaccination.
• Healthy participants or participants with mild underlying disease \[in a stable state without exacerbation (no admission to hospital or no major adjustment to treatment regimen, etc.) for at least 3 months prior to enrollment in this study\].
• Participants who have vaccinated 2 doses of CoronaVac® (with an interval of 3-8 weeks between 2 doses), for 6-12 months prior to enrollment.

You may not qualify if:

• Previous medications intervention for the prophylaxis or prevention of COVID-19 (Including vaccination with any licensed SARS-CoV-2 vaccines other than 2 doses of CoronaVac® ).
• History of Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS) or other coronavirus infections.
• History of a previous laboratory-confirmed diagnosis of SARS-CoV-2 infection or COVID-19.
• History of allergy to any component of the study vaccine or history of severe allergic reaction to the vaccine or drug (including but not limited to anaphylaxis, allergic laryngeal oedema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (Arthus reaction)).
• Positive nucleic acid for SARS-CoV-2 in nasopharyngeal/oropharyngeal swab specimens.
• Positive HIV test result.
• A history or family history of convulsions, epilepsy, encephalopathy and psychosis.
• Malignant tumors in the active phase, malignant tumors not receiving adequate treatment, malignant tumors at potential risk of recurrence during the study period.
• Congenital or functional splenic deficiency, complete or partial splenectomy for any reason.
• Prolonged (defined as more than 14 days) use of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, inhaled and topical steroids are permitted) within 6 months prior to the vaccine.
• Any other licensed vaccines given within 28 days prior to the study vaccination, or planned administration of vaccine(s) within 28 days after vaccination.
• Have received immunoglobulin or other blood products within 3 months prior to enrollment or plan to receive them during the study period.
• Blood donation or blood loss ≥ 450 mL within 1 month prior to enrolment, or planned donation during the study period.
• Participants who have received any other investigational product within 1 month prior to enrollment or intent to participate in another clinical study at any time during the conduct of this study.
• Female participants who are pregnant or breastfeeding.

Sponsors & Collaborators

• AIM Vaccine Co., Ltd.: lead

Study Sites (1)

Clinical Trial Unit, National Institute of Health

Islamabad, 45500, Pakistan

Location

MeSH Terms

Interventions

LVRNA009 COVID-19 vaccine; sinovac COVID-19 vaccine

Study Officials

• Aamer Ikram

  National Institute of Health, Islamabad

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Fan Zhang

CONTACT

021-33360772; fan.zhang@aimbio.com

Wumei Han

CONTACT

021-33360772; wumei.han@aimbio.com

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: A randomized, blinded, parallel-controlled design

Study Record Dates

• First Submitted: June 14, 2022
• First Posted: June 23, 2022
• Study Start: April 1, 2023
• Primary Completion: October 1, 2023
• Study Completion: October 1, 2024
• Last Updated: February 2, 2023

Record last verified: 2022-06

Locations

PA (1)