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A Study to Evaluate Efficacy, Immunogenicity and Safety of a Recombinant Respiratory Syncytial Virus Vaccine in Older Adults Aged 60 Years and Older

30. oktober 2026 oppdatert av: Guangzhou Patronus Biotech Co., Ltd.

A Randomized, Observer-blind, Placebo-controlled Phase III Clinical Trial to Evaluate the Efficacy, Immunogenicity, and Safety of the Respiratory Syncytial Virus (RSV) Vaccine, LYB005 in Older Adults Aged 60 Years and Older

This is a randomized, observer-blinded, placebo-controlled Phase III clinical trial to evaluate efficacy, immunogenicity and safety of the Respiratory Syncytial Virus (RSV) Vaccine, LYB005 in participants aged 60 years and older.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

A randomized, observer-blinded, placebo-controlled trial will be conducted to observe efficacy, immunogenicity and safety of LYB005 in adults aged 60 years and older. A total of 25000 participants aged 60 years and older will be enrolled. All participants will randomly receive the investigational vaccine and the placebo in a 1:1 ratio.

Studietype

Intervensjonell

Registrering (Antatt)

25000

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Jiangsu
      • Nanjing, Jiangsu, Kina
        • Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine)
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

60 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • A male or female participant aged 60 years and above;
  • Participants can provide valid identification, voluntarily agree to participate in the study, and sign the Informed Consent Form, and are able to attend all planned follow-up visits and comply with the protocol requirements;
  • Axillary temperature ≤ 37.0°C on the day of enrollment;
  • Female participants should have been menopausal or have undergone sterilization surgery; Menopause is defined as the absence of menstruation for at least 12 consecutive months without alternative medical measures; sterilization surgeries include bilateral tubal ligation or bilateral oophorectomy or hysterectomy; Male participants must not plan to father a child from the time of screening until 30 days after vaccination;
  • Participants in the trial who were judged by the researchers to be healthy or have stable health conditions. [Stable health condition: This refers to having a chronic disease and maintaining a stable condition within the three months prior to enrollment irrespective of receipt of specific treatment, such as diabetes, hypertension, chronic obstructive pulmonary disease, and asthma. If the researcher determines that the condition is stable, participation in this trial will be permitted.].

Exclusion Criteria:

  • Participants who are known to be allergic to any of the components contained in the test vaccine (e.g., sucrose, polysorbate 20, sodium dihydrogen phosphate dihydrate, and disodium hydrogen phosphate dihydrate.); A history of severe allergic reactions or serious adverse reactions to any vaccine;
  • A confirmed diagnosis or etiological evidence of respiratory syncytial virus infection and related diseases caused by the infection within 12 months before enrollment (confirmed by RT-PCR, RSV-Ab, etc.);
  • Have received or plan to receive any marketed or experimental RSV vaccine/RSV prophylactic medication;
  • Has taken antipyretics, analgesics (except for medications used for underlying conditions that, in the investigator's judgment, are unlikely to affect study outcomes, such as enteric-coated aspirin for the prevention of cardiovascular and cerebrovascular diseases.) or anti-allergy drugs within 3 days before enrollment;
  • Receipt of any non-live vaccine within 14 days prior to enrollment, or any live or nucleic acid vaccine within 28 days prior to enrollment;
  • Any non-specific immunoglobulins and/or blood products containing non-specific immunoglobulins (such as whole blood, plasma) have been used within 3 months prior to enrollment or are planned to be used during the trial;
  • Individual with the following diseases: ①Has acute diseases or are in the acute exacerbation period of chronic diseases within 3 days before vaccination; ②Individual with active tuberculosis or currently undergoing treatment for tuberculosis; ③History of congenital or acquired immunodeficiency or autoimmune diseases; Chronic administration (≥14 consecutive days) of corticosteroids (dose ≥ 20 mg/day prednisone or equivalent dose) or other immunomodulatory medications within the past 3 months, currently using or planning to use a long-acting immunomodulatory agent (e.g., infliximab), with the exception of inhaled or topical steroids, or short-term use (<14 consecutive days) of oral corticosteroids; ④Previous or current neurological disorders resulting in damage to brain nervous tissue (including seizures [specifically excluding simple febrile seizures in children], encephalopathy, etc.); or uncontrolled epilepsy with seizures occurring within 1 year prior to enrollment; or a history of psychotic disorders that affect normal behavior; ⑤Asplenia or functional asplenia; ⑥ Any cardiovascular, respiratory, hepatic, renal, metabolic, hematologic, or lymphatic disease deemed by the investigator to be unstable or uncontrolled (defined as requiring a major adjustment in treatment regimen within 3 months prior to enrollment, or hospitalization due to disease worsening; Individual with a history of lacunar cerebral infarction or cerebral infarction without residual sequelae can be enrolled if, after careful evaluation by the investigator, the condition has remained stable without recurrence for at least 5 years prior to enrollment); Individual with active malignancy or currently receiving antineoplastic therapy (excluding adjuvant endocrine therapy) are excluded (Certain malignancies, such as carcinoma in situ that has been clinically cured or papillary thyroid carcinoma, can be permitted following careful investigator assessment if there is no evidence of recurrence for ≥5 years prior to enrollment); ⑦Coagulation disorders (e.g., hemophilia or platelet count < 50 × 10⁹/L) that are contraindications for intramuscular injection; ⑧Uncontrolled hypertension as determined by the investigator (measured on-site: systolic blood pressure ≥ 160 mmHg and/or diastolic blood pressure ≥ 100 mmHg whether or not receiving medication); ⑨Arrhythmias that are newly diagnosed within 3 months prior to enrollment, not adequately controlled, or have required modification of treatment within 3 months prior to enrollment;
  • Oxygen saturation (SpO₂) ≤ 90% as measured on site;
  • History of major surgery within 6 months prior to enrollment (as determined by the investigator), or not fully recovered from the surgery, or having plans for major surgery during the study;
  • A history of alcohol consumption and/or drug abuse that, in the investigator's judgment, may affect study assessments or participant compliance (Note: Within 3 months prior to enrollment, average weekly alcohol consumption exceeding 21 units for males or 14 units for females, where 1 unit = 360 mL of beer, 45 mL of spirits containing 40% alcohol, or 150 mL of wine. Drug abuse refers to the repeated and excessive use of drugs with dependence-producing properties or dependence potential, unrelated to recognized medical needs and for non-medical purposes);
  • Individual who is currently participating in other clinical studies, or plan to participate in other clinical studies before the end of this clinical study;
  • Other conditions that may impact the participant's safety or influence the assessment of vaccine response, as determined by the investigator.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: LYB005

Participant aged 60 years and older will be vaccinated with 1 dose of LYB005 at Day 0.

0.5 mL per dose.

Placebo komparator: Placebo

Participants aged 60 years and older will be vaccinated with 1 dose of placebo at Day 0.

0.5 mL 0.9% sodium chloride (normal saline) injection per dose

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of first episode of RSV-associated lower respiratory tract disease (RSV-LRTD) from 14 days post-vaccination through the end of the first RSV season
Tidsramme: From 14 days post-vaccination through the end of the first RSV season

First episode of Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)-confirmed RSV A and/or RSV B- associated LRTD from 14 days post-vaccination through the end of the first RSV season was assessed. The case definition for RSV-confirmed LRTD is as follows: Presence of at least one RSV-positive swab detected by RT-PCR.

From 14 days post-vaccination through the end of the first RSV season

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Immediate adverse events (AEs) within 30 minutes after vaccination
Tidsramme: 30 mins after vaccination

The incidence, severity and causality of any AEs within 30 minutes after vaccination

30 mins after vaccination
Solicited local and systemic AEs
Tidsramme: Within 7 days after vaccination

The incidence, severity and causality of any solicited local and systemic AEs within 7 days after vaccination

Within 7 days after vaccination
Unsolicited AEs
Tidsramme: Within 30 days after vaccination

The incidence, severity and causality of any unsolicited AEs within 30 days after vaccination.

Within 30 days after vaccination
Serious adverse events (SAEs) and adverse events of special interest (AESIs)
Tidsramme: 12 months after vaccination

The incidence and causality of any SAEs and AESIs

12 months after vaccination
Incidence of first episode of RSV-associated severe LRTD (RSV-sLRTD) from 14 days post-vaccination through the end of the first RSV season
Tidsramme: From 14 days post-vaccination through the end of the first RSV season

RT-PCR-confirmed RSV A and/or RSV B-sLRTD is assessed.

From 14 days post-vaccination through the end of the first RSV season
Incidence of first episode of RT-PCR confirmed RSV A and/or B associated acute respiratory infections (ARI) from 14 days post-vaccination through the end of the first RSV season
Tidsramme: From 14 days post-vaccination through the end of the first RSV season

RT-PCR-confirmed RSV A and/or RSV B-ARI is assessed.

From 14 days post-vaccination through the end of the first RSV season
The geometric mean titer (GMT) of Neutralizing Antibodies against RSV A and RSV B
Tidsramme: Before vaccination, 14 days, 30 days, 12 months and 24 months after vaccination

Measured by microneutralization assay.

Before vaccination, 14 days, 30 days, 12 months and 24 months after vaccination
Geometric mean fold rise (GMFR) for Neutralizing Antibodies against RSV A and RSV B
Tidsramme: 14 days, 30 days, 12 months and 24 months after vaccination

Change from prevaccination in geometric mean fold rise of Neutralizing antibody titer against RSV A and RSV B

14 days, 30 days, 12 months and 24 months after vaccination
The geometric mean concentration (GMC) for Pre-fusion Protein Specific Binding Antibodies
Tidsramme: Before vaccination, 14 days, 30 days, 12 months and 24 months after vaccination

Measured by Enzyme-Linked Immunosorbent Assay (ELISA).

Before vaccination, 14 days, 30 days, 12 months and 24 months after vaccination
GMFR for Pre-fusion Protein Specific Binding Antibodies
Tidsramme: 14 days, 30 days, 12 months and 24 months after vaccination

Change from prevaccination in geometric mean fold rise of Pre-fusion Protein Specific Binding Antibodies

14 days, 30 days, 12 months and 24 months after vaccination

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

1. september 2027

Studiet fullført (Antatt)

1. desember 2027

Datoer for studieregistrering

Først innsendt

26. oktober 2026

Først innsendt som oppfylte QC-kriteriene

26. oktober 2026

Først lagt ut (Faktiske)

2. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

3. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • LYB005/CT-CHN-301

Plan for individuelle deltakerdata (IPD)

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UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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