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New Data for AREXVY, GSK’s Respiratory Syncytial Virus Vaccine, Show Potential to Help Protect a Broader Group of Adults at Increased Risk for RSV Disease

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GSK announced new preliminary data for AREXVY, its RSV vaccine, showing promising results in two key populations: adults aged 18-49 with risk factors and immunocompromised adults. A single dose demonstrated robust immune response in at-risk adults 18-49, while immunocompromised adults showed positive results with two doses. The vaccine's potential expansion could benefit over 21 million at-risk adults aged 18-49 in the US alone. Currently approved for adults 60+ in over 50 countries and at-risk adults 50-59 in select regions, these new data support potential broader application. The safety profile remained consistent with previous trials, showing mainly mild, transient effects.

GSK ha annunciato nuovi dati preliminari per AREXVY, il suo vaccino RSV, mostrando risultati promettenti in due popolazioni chiave: adulti tra i 18 e i 49 anni con fattori di rischio e adulti immunocompromessi. Una singola dose ha dimostrato una robusta risposta immunitaria negli adulti a rischio tra i 18 e i 49 anni, mentre gli adulti immunocompromessi hanno mostrato risultati positivi con due dosi. L'espansione potenziale del vaccino potrebbe beneficiare oltre 21 milioni di adulti a rischio tra i 18 e i 49 anni solo negli Stati Uniti. Attualmente approvato per adulti di età pari o superiore a 60 anni in oltre 50 paesi e per adulti a rischio tra i 50 e i 59 anni in alcune regioni selezionate, questi nuovi dati supportano una possibile applicazione più ampia. Il profilo di sicurezza è rimasto coerente con i trial precedenti, mostrando principalmente effetti lievi e transitori.

GSK anunció nuevos datos preliminares para AREXVY, su vacuna contra el VRS, mostrando resultados prometedores en dos poblaciones clave: adultos de 18 a 49 años con factores de riesgo y adultos inmunocomprometidos. Se demostró que una sola dosis generaba una respuesta inmune robusta en adultos en riesgo de 18 a 49 años, mientras que los adultos inmunocomprometidos mostraron resultados positivos con dos dosis. La posible expansión de la vacuna podría beneficiar a más de 21 millones de adultos en riesgo de 18 a 49 años solo en EE.UU. Actualmente, está aprobada para adultos mayores de 60 años en más de 50 países y para adultos en riesgo de 50 a 59 años en regiones seleccionadas; estos nuevos datos respaldan una posible aplicación más amplia. El perfil de seguridad se mantuvo consistente con ensayos anteriores, mostrando principalmente efectos leves y transitorios.

GSK는 자사의 RSV 백신 AREXVY에 대한 새로운 초기 데이터를 발표했으며, 두 가지 주요 집단인 18-49세의 위험 요소가 있는 성인과 면역력이 저하된 성인에서 유망한 결과를 보였습니다. 한 번의 투여로 위험에 처한 18-49세 성인에서 강력한 면역 반응이 나타났고, 면역력이 저하된 성인은 두 번의 투여로 긍정적인 결과를 보였습니다. 백신의 잠재적 확장은 미국 내에서만 2100만 명 이상의 위험에 처한 18-49세 성인에게 혜택을 줄 수 있습니다. 현재 60세 이상 성인을 위해 50개국 이상에서 승인되었고, 위험 요소가 있는 50-59세 성인에 대해서는 일부 지역에서 승인되었습니다. 이러한 새로운 데이터는 보다 광범위한 적용 가능성을 지지합니다. 안전성 프로필은 이전 시험과 일관되게 유지되었으며, 주로 경미하고 일시적인 효과를 보였습니다.

GSK a annoncé de nouvelles données préliminaires pour AREXVY, son vaccin contre le VRS, montrant des résultats prometteurs dans deux populations clés : des adultes âgés de 18 à 49 ans avec des facteurs de risque et des adultes immunodéprimés. Une seule dose a démontré une réponse immunitaire robuste chez les adultes à risque âgés de 18 à 49 ans, tandis que les adultes immunodéprimés ont montré des résultats positifs avec deux doses. L'expansion potentielle du vaccin pourrait bénéficier à plus de 21 millions d'adultes à risque âgés de 18 à 49 ans rien qu'aux États-Unis. Actuellement approuvé pour les adultes de 60 ans et plus dans plus de 50 pays et pour les adultes à risque de 50 à 59 ans dans certaines régions, ces nouvelles données soutiennent une application potentiellement plus large. Le profil de sécurité est resté cohérent avec les essais antérieurs, montrant principalement des effets légers et transitoires.

GSK hat neue vorläufige Daten für die AREXVY, ihren RSV-Impfstoff, bekannt gegeben, die vielversprechende Ergebnisse in zwei Schlüsselgruppen zeigen: Erwachsene im Alter von 18 bis 49 Jahren mit Risikofaktoren und immungeschwächte Erwachsene. Eine Einzelimpfung führte zu einer robusten Immunantwort bei gefährdeten Erwachsenen im Alter von 18 bis 49 Jahren, während immungeschwächte Erwachsene mit zwei Dosen positive Ergebnisse zeigten. Die potenzielle Ausweitung des Impfstoffs könnte über 21 Millionen gefährdete Erwachsene im Alter von 18 bis 49 Jahren allein in den USA zugutekommen. Der Impfstoff ist derzeit in über 50 Ländern für Erwachsene ab 60 Jahren und in ausgewählten Regionen für gefährdete Erwachsene im Alter von 50 bis 59 Jahren zugelassen, diese neuen Daten unterstützen eine potenziell breitere Anwendung. Das Sicherheitsprofil blieb konsistent mit früheren Studien und zeigte hauptsächlich milde, vorübergehende Nebenwirkungen.

Positive
  • Potential market expansion to include 21+ million at-risk adults aged 18-49 in the US
  • Single dose showed robust immune response in adults 18-49 at increased risk
  • Successful immune response in immunocompromised adults with two doses
  • Consistent safety profile with previous clinical trials
Negative
  • Additional dose requirement for immunocompromised patients may increase treatment costs

Insights

The preliminary clinical trial data for AREXVY demonstrates significant potential for market expansion. The vaccine shows robust immune response in two key populations: adults 18-49 with risk factors and immunocompromised individuals. With 21 million at-risk adults aged 18-49 in the US alone, this represents a substantial market opportunity.

The trial data's strength lies in meeting non-inferiority endpoints compared to older adults and showing consistent immune responses across RSV subtypes. The safety profile aligns with previous studies, which is important for regulatory approval. The potential label expansion to include younger at-risk adults and immunocompromised patients could significantly increase AREXVY's addressable market, particularly given the lack of competing vaccines for these populations.

This development positions GSK to potentially capture an untapped market segment. The expansion into younger at-risk populations could drive substantial revenue growth, considering the complete absence of approved RSV vaccines for adults under 60 with risk factors. The successful trials in immunocompromised patients further differentiate AREXVY in the competitive landscape.

GSK's strategic timing is notable, as they're moving quickly to expand their first-mover advantage in the RSV vaccine space. The robust data and planned regulatory submissions suggest potential label updates could come within the next 12-18 months, allowing GSK to strengthen its market position before competitors can catch up.

  • Single dose of vaccine elicited robust immune response with acceptable safety profile in adults aged 18-49 at increased risk for RSV-LRTD
  • Two doses of vaccine in immunocompromised adults aged 18 and older elicited immune responses similar to one dose in healthy adults aged 50+ and with an acceptable safety profile
  • In the US alone, adults aged 18-49 with at least one risk factor for RSV disease could exceed 21 million1

PHILADELPHIA--(BUSINESS WIRE)-- GSK plc (LSE/NYSE: GSK) today announced new preliminary data for AREXVY (Respiratory Syncytial Virus Vaccine, Adjuvanted) in adults aged 18-49 at increased risk for lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) due to certain underlying medical conditions and in adults who are immunocompromised. These data show the vaccine’s potential to help protect a broader group of adults at risk from the potentially serious consequences of RSV. In the US alone, the number of adults aged 18-49 with at least one risk factor that could put them at risk for RSV disease could exceed 21 million.1

The vaccine is currently approved for active immunization for the prevention of RSV-LRTD caused by RSV in adults aged 60 and older in over 50 countries, and in adults aged 50-59 at increased risk in a number of countries including the US and in Europe*. There are currently no RSV vaccines recommended for adults younger than 60 years of age who are at increased risk for RSV disease, despite the burden of disease in this population.

Tony Wood, Chief Scientific Officer, GSK, said: “These promising data add to the evidence supporting GSK’s RSV vaccine and could help expand protection to more adults at risk from RSV disease. They also provide valuable insights into the potential impact of a second dose for certain populations. We’re committed to working with health authorities and regulators to help adults at increased risk of RSV disease benefit from vaccination.”

In the phase IIIb trial (NCT063894872) a single dose of the vaccine elicited robust immune responses in adults aged 18-49 at increased risk for RSV-LRTD due to certain underlying medical conditions (n=395). The immune response was non-inferior to that observed in adults aged 60 and older (n=417), meeting the trial’s co-primary endpoints.

In the phase IIb trial (NCT059219033) a single dose of the vaccine showed a robust immune response in adults aged 18 and older who are immunocompromised due to kidney or lung transplant (n=131), with a second dose (n=130) eliciting responses similar to those of healthy adults aged 50 and older who received one dose (n=125). These immune responses were consistent for RSV-A and RSV-B subtypes in all groups (those who received 1 or 2 doses). These data will be presented today at the meeting of the CDC’s Advisory Committee on Immunization Practices.

In both studies, the safety and reactogenicity data were consistent with results from the phase III program that have supported the initial approval of the vaccine. The most common local adverse event was pain, and the most common systemic adverse events were fatigue, myalgia, arthralgia and headache, most of which were transient and mild in intensity.

RSV is a common, contagious virus that can cause severe respiratory illness and impacts an estimated 64 million people of all ages globally every year.4 Immunocompromised people and those with certain underlying medical conditions, such as chronic obstructive pulmonary disease (COPD), asthma, heart failure and diabetes are at increased risk for severe consequences from an RSV infection compared to those without these conditions,5, 6 including having a higher risk of mortality.7

Final results from these trials will be presented at upcoming medical conferences and submitted for peer-reviewed publication. The final data will also be submitted to the US Food and Drug Administration (FDA) and other regulators to support potential label updates.

About the trial designs

NCT06389487 is a phase IIIb open-label study to evaluate the non-inferiority of the immune response and to evaluate the safety of the GSK’s RSV vaccine in adults aged 18-49 at increased risk for RSV disease (n=395) compared to adults aged 60 and older (n=417). 1,457 participants were enrolled across 52 locations in 6 countries.

The trial’s co-primary endpoints were RSV-A and RSV-B neutralization titers expressed as mean geometric titer ratio (relative to older adults over adults at increased risk) and sero-response in RSV-A and RSV-B neutralizing titers one month post vaccine administration. There were also safety and immunogenicity secondary endpoints. An additional cohort of 601 participants aged 18-49 were followed up for adverse events separate to safety follow up of the initial cohort. The study is ongoing to collect further safety and immunogenicity data up to 6 months post vaccination and is expected to finish in 2025.

NCT05921903 is a phase IIb, randomized, controlled, open-label, multi-country study to evaluate the immune response and safety of GSK’s RSV vaccine in adults (≥18 years of age) who are immunocompromised due to lung and renal transplant, comparing 1 versus 2 doses (1 dose, n=131, 2 doses, n=130) one month (30-42 days) after the second vaccine administration compared to a control group of non-immunocompromised adults aged 50 and older receiving a single dose of GSK’s RSV vaccine (n=125 non-immunocompromised adults aged 50 and older). 386 participants were enrolled across 48 locations in 8 countries.

The trial’s co-primary endpoints were RSV-A and RSV-B neutralization titers following a first and a second dose of GSK’s RSV vaccine expressed as mean geometric increase post dose 2 relative to post dose 1 at approximatively one month. There were also safety and immunogenicity secondary endpoints. The study is ongoing to collect further safety and immunogenicity data up to 12 months post last dose and is expected to finish in 2025.

About AREXVY (Respiratory Syncytial Virus Vaccine, Adjuvanted)
AREXVY contains recombinant RSV glycoprotein F stabilized in the prefusion conformation (RSVPreF3). This antigen is combined with GSK’s proprietary AS01E adjuvant.

The use of this vaccine should be in accordance with official recommendations. As with any vaccine, a protective immune response may not be elicited in all vaccinees.

The vaccine has been approved for the prevention of RSV-LRTD in individuals 60 years of age and older in more than 50 countries, including in Europe, Japan and US. In addition, it is approved in the US and EU/EEA countries for use in individuals aged 50-59 who are at increased risk due to certain underlying medical conditions. Regulatory reviews for this extended indication are also undergoing review in other countries – including Japan. The proposed trade name remains subject to regulatory approval in other markets.

The GSK proprietary AS01 adjuvant system contains STIMULON QS-21 adjuvant licensed from Antigenics Inc, a wholly owned subsidiary of Agenus Inc. STIMULON is a trademark of SaponiQx Inc., a subsidiary of Agenus.

Indication for AREXVY
AREXVY is a vaccine indicated for active immunization for the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in:

  • Individuals 60 years of age and older;
  • Individuals 50 through 59 years of age who are at increased risk for LRTD caused by RSV.

Important Safety Information for AREXVY

  • AREXVY is contraindicated in anyone with a history of a severe allergic reaction (eg, anaphylaxis) to any component of AREXVY
  • Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions following administration of AREXVY
  • Syncope (fainting) may occur in association with administration of injectable vaccines, including AREXVY. Procedures should be in place to avoid injury from fainting
  • Immunocompromised persons, including those receiving immunosuppressive therapy, may have a diminished immune response to AREXVY
  • In adults 60 years of age and older, the most commonly reported adverse reactions (≥10%) were injection site pain (60.9%), fatigue (33.6%), myalgia (28.9%), headache (27.2%), and arthralgia (18.1%)
  • In adults 50 through 59 years of age, the most commonly reported adverse reactions (≥10%) were injection site pain (75.8%), fatigue (39.8%), myalgia (35.6%), headache (31.7%), arthralgia (23.4%), erythema (13.2%), and swelling (10.4%)
  • There are no data on the use of AREXVY in pregnant or breastfeeding individuals. AREXVY is not approved for use in persons <50 years of age
  • Vaccination with AREXVY may not result in protection of all vaccine recipients

Please see full Prescribing Information for AREXVY.

About GSK
GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. Find out more at gsk.com.

Cautionary statement regarding forward-looking statements
GSK cautions investors that any forward-looking statements or projections made by GSK, including those made in this announcement, are subject to risks and uncertainties that may cause actual results to differ materially from those projected. Such factors include, but are not limited to, those described under Item 3.D “Risk factors” in GSK’s Annual Report on Form 20-F for 2023, and GSK’s Q2 Results for 2024.

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Notes:
* European Union member states, as well as in the European Economic Area (EEA) countries Iceland, Norway and Liechtenstein.

References

1 Based on a study focusing on US adults aged 20-49. Among adults aged 20-49 years in the US, a total of 17.0% (N=21 million/125 million) had at least one diagnosed risk factor for severe RSV disease (including CHF, CHD, stroke, angina, MI, COPD, current asthma, diabetes, current liver disease, and/or renal disease) – in [E.Horn et al, “Characteristics Associated with the Presence of One or More Risk Factors for Severe Respiratory Syncytial Virus Disease among Adults in the United States”, poster presented at ID Week poster [available on demand: P691 - https://idweek2024.eventscribe.net/index.asp]
2 Clinicaltrials.gov, “A Study on the Immune Response and Safety of Vaccine Against Respiratory Syncytial Virus (RSV) Given to Adults 18 to 49 Years of Age at Increased Risk for Respiratory Syncytial Virus Disease, Compared to Older Adults 60 Years of Age and Above” – available at: https://clinicaltrials.gov/study/NCT06389487
3 Clinicaltrials.gov, “A Study on the Immune Response and Safety of an RSV Vaccine When Given to Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant and Are at an Increased Risk of Respiratory Syncytial Virus Lower Respiratory Tract Disease and Compared to Healthy Adults 50 Years of Age and Above (RSV OA=ADJ-023)” – available at: https://clinicaltrials.gov/study/NCT05921903
4 National Institute of Allergy and Infectious Diseases, Respiratory Syncytial Virus (RSV). Available at: https://www.niaid.nih.gov/diseases-conditions/respiratory-syncytial-virus-rsv – last accessed: September 2024
5 Branche AR et al., Incidence of Respiratory Syncytial Virus Infection Among Hospitalized Adults, 2017–2020 in Clinical Infectious Diseases, 2022:74:1004–1011
6 CDC, Clinical overview of RSV. Available at: https://www.cdc.gov/rsv/hcp/clinical-overview/index.html. Last accessed: October 2024
7 A.Njue et al., “Systematic Literature Review of Risk Factors for Poor Outcomes Among Adults With Respiratory Syncytial Virus Infection in High-Income Countries” in Open Forum Infectious Diseases, Volume 10, Issue 11, November 2023, ofad513, https://doi.org/10.1093/ofid/ofad513

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Source: GSK plc

FAQ

What are the new findings for GSK's AREXVY RSV vaccine?

New data shows AREXVY elicits robust immune response in adults aged 18-49 at increased risk for RSV-LRTD and in immunocompromised adults, with acceptable safety profiles in both populations.

How many doses of AREXVY (GSK) are needed for immunocompromised patients?

According to the trial results, immunocompromised adults require two doses of AREXVY to achieve immune responses similar to those seen in healthy adults aged 50+ who received one dose.

What is the current approval status of GSK's AREXVY vaccine?

AREXVY is currently approved for adults 60 and older in over 50 countries, and for at-risk adults aged 50-59 in several countries including the US and Europe.

What is the market potential for AREXVY (GSK) in the US for adults aged 18-49?

In the US alone, over 21 million adults aged 18-49 with at least one risk factor could potentially benefit from AREXVY vaccination against RSV disease.

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