GSK Announces Positive Topline Data on Co-Administration of AREXVY and SHINGRIX

Rhea-AI Summary

GSK announced positive topline data from a phase 3 trial evaluating the co-administration of AREXVY (RSV vaccine) and SHINGRIX (shingles vaccine) in adults 50 years and older. The study met its primary endpoint, showing a non-inferior immune response when the vaccines were given together compared to separate administration. Co-administration was well-tolerated with acceptable safety profiles.

Key findings include:

• Comparable immune responses in co-administration and separate administration groups
• Most common adverse events: injection site pain, fatigue, and myalgia
• Similar duration of adverse events across groups

GSK plans to submit these results to support regulatory submissions to the FDA, EMA, and other regulators. The company aims to reduce barriers to adult immunization by potentially decreasing the number of healthcare visits required for vaccination.

Positive

• Phase 3 trial met primary endpoint, showing non-inferior immune response for co-administered AREXVY and SHINGRIX
• Co-administration of vaccines was well-tolerated with acceptable safety profiles
• Results support potential for reducing number of healthcare visits for adult vaccinations
• Data to be submitted for regulatory approvals, potentially expanding vaccine administration options

Negative

• None.

Medical Research Analyst

This positive topline data on co-administration of AREXVY and SHINGRIX is highly significant for GSK's vaccine portfolio. The study's success in meeting its primary endpoint of non-inferior immune response for both vaccines when co-administered is a major clinical milestone. This could potentially streamline vaccination schedules for older adults, improving compliance and coverage rates.

The well-tolerated safety profile and acceptable reactogenicity are important factors that could enhance patient and healthcare provider confidence in co-administration. The most common adverse events reported (injection site pain, fatigue and myalgia) are typical for vaccines and don't raise new safety concerns.

This data could lead to updated clinical guidelines and potentially new regulatory approvals, allowing for more efficient vaccination strategies. It's a significant step towards addressing the undervaccination issue in adults, which could have substantial public health implications, especially considering the high disease burden of RSV (177,000 hospitalizations and 14,000 deaths annually in the US for those 65+) and shingles (1 million cases annually in the US).

Financial Analyst

This positive data represents a significant commercial opportunity for GSK. Co-administration of AREXVY and SHINGRIX could potentially boost sales of both vaccines by simplifying the vaccination process for patients and healthcare providers. This could lead to increased market penetration and higher vaccination rates.

The timing is strategic, coming shortly after AREXVY's approval, potentially accelerating its market adoption. SHINGRIX, already a blockbuster vaccine for GSK, could see renewed growth. In Q2 2023, SHINGRIX sales were 880 million, up 11% year-over-year. AREXVY, launched in Q3 2023, is expected to be a major growth driver.

This development could give GSK a competitive edge in the adult vaccine market, potentially increasing market share and strengthening its position against competitors like Pfizer and Moderna. Investors should watch for potential regulatory approvals and guideline updates, which could further boost the commercial prospects of these vaccines.

Public Health Expert

This co-administration data is a game-changer for adult immunization strategies. It addresses a critical barrier to adult vaccination: the need for multiple healthcare visits. By potentially reducing the number of visits required, this approach could significantly improve vaccination rates among older adults, a population often under-protected against preventable diseases.

The implications for public health are substantial. Higher vaccination rates against RSV and shingles could lead to reduced hospitalizations, lower healthcare costs and improved quality of life for older adults. This is particularly important given the aging global population and the increasing burden of these diseases.

Moreover, this approach aligns with the World Health Organization's Immunization Agenda 2030, which emphasizes the importance of life-course immunization. It could serve as a model for future vaccine co-administration studies, potentially leading to more efficient immunization programs across various age groups and diseases. Public health officials and policymakers should closely monitor these developments for potential integration into national immunization strategies.

• Trial met primary endpoint, non-inferior immune response for both vaccines when co-administered compared with separate administration
• Co-administration of the RSV and shingles adjuvanted vaccines was well tolerated, with acceptable reactogenicity and safety profiles
• These data advance the science of co-administration of recommended adult vaccines

PHILADELPHIA--(BUSINESS WIRE)-- GSK plc (LSE/NYSE: GSK) today announced positive topline data from the phase 3 trial in adults 50 years and older evaluating the immunogenicity, reactogenicity and safety of AREXVY (Respiratory Syncytial Virus Vaccine, Adjuvanted) when co-administered with SHINGRIX (Zoster Vaccine Recombinant, Adjuvanted), both AS01-adjuvanted vaccines (NCT05966090).^1,2 The data were presented as a late-breaking abstract at the European Geriatric Medicine Society (EuGMS) Congress in Valencia, Spain (September 18-20th, 2024).² SHINGRIX is approved for the prevention of shingles (herpes zoster) in adults aged 50 years and older. AREXVY is approved for the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in individuals 60 years of age and older, as well as individuals 50 through 59 years of age who are at increased risk for LRTD caused by RSV.

The data showed a non-inferior immune response when the vaccines were co-administered compared to when they were administered at separate visits.² Co-administration was also well tolerated, with acceptable reactogenicity and safety profiles.² In both groups, the most frequently reported adverse events were pain at the injection site, fatigue, and myalgia.² The duration of solicited adverse events was comparable across the two groups.²

Len Friedland, MD, Vice President of Scientific Affairs and Public Health, GSK, said: “We are excited to share data on the co‑administration of our RSV and shingles vaccines. Adult immunization offers immense individual and societal benefits and yet, vaccination rates for adults are often inadequate. With our co-administration studies, GSK is using its science and technology to help remove barriers to adult immunization, by potentially reducing the number of visits to the healthcare offices and pharmacies and ultimately help to get ahead of RSV and shingles.”

Results from this trial will be submitted for peer-reviewed scientific publication and will be used to support regulatory submissions to the US Food and Drug Administration (FDA), the European Medicines Agency (EMA), and other regulators.

Both RSV and shingles pose significant health risks to older adults, and these risks only increase with age as the immune system declines. Immunocompromised individuals and those with certain underlying medical conditions—for example, asthma and COPD—may also be at increased risk for these diseases.^3,4,5 RSV is a common, contagious respiratory virus that can lead to potentially serious respiratory illness.³ Each year, approximately 177,000 adults 65 years and older are hospitalized in the US due to RSV and an estimated 14,000 of those cases result in death.⁶ Shingles is a painful, blistering rash that can last for weeks. Because it is caused by the reactivation of the varicella zoster virus (VZV)—the same virus that causes chickenpox—99% of US adults have the virus that causes shingles inside their body, although not everyone will develop shingles.⁷ An estimated one million people develop shingles annually in the US.⁸

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 vaccine has been approved for the prevention of RSV-LRTD in individuals 60 years of age and older in 50 countries, including Europe, Japan and US. It is also approved in several countries for use in adults aged 50–59 at increased risk for RSV-LRTD, including European Union/European Economic Area and US. Regulatory reviews in multiple countries are ongoing. The proposed trade name remains subject to regulatory approval in other markets.

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

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 SHINGRIX (Recombinant Zoster Vaccine or RZV)
SHINGRIX is a non-live, recombinant subunit vaccine indicated for the prevention of shingles in adults 50 and over. It combines an antigen, glycoprotein E, with an adjuvant system, AS01_B, and may help overcome the natural age-related decline in responses to immunization that contributes to the challenge of protecting adults aged 50 and over from shingles.^9,10 RZV is not indicated to prevent primary varicella infection (chickenpox). In several countries, it is also approved for adults aged 18 years or over at increased risk for shingles. The use of RZV should be in accordance with official recommendations and local product label.

Indication for SHINGRIX
SHINGRIX is an FDA-approved vaccine for the prevention of shingles (herpes zoster) in:

• Adults 50 years and older.
• Adults 18 years and older who are or will be at increased risk of shingles due to being immunocompromised by known disease or therapy.

SHINGRIX is not used to prevent chickenpox.

Important Safety Information for SHINGRIX

• SHINGRIX is contraindicated in anyone with a history of a severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine or after a previous dose of SHINGRIX.
• Review immunization history for possible vaccine sensitivity and previous vaccination-related adverse reactions. Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of SHINGRIX.
• In a post marketing observational study, an increased risk of Guillain-Barré syndrome was observed during the 42 days following vaccination with SHINGRIX.
• Syncope (fainting) can be associated with the administration of vaccines, including SHINGRIX. Procedures should be in place to avoid falling injury and to restore cerebral perfusion following syncope.
• In individuals aged 50 years and older: Solicited local adverse reactions were pain, redness, and swelling. Solicited general adverse reactions were myalgia, fatigue, headache, shivering, fever, and gastrointestinal symptoms.
• The data are insufficient to establish if there is vaccine-associated risk with SHINGRIX in pregnant women.
• It is not known whether SHINGRIX is excreted in human milk. Data are not available to assess the effects of SHINGRIX on the breastfed infant or on milk production/excretion.
• Vaccination with SHINGRIX may not result in protection of all vaccine recipients.

Please see full Prescribing Information for SHINGRIX.

About the NCT05966090 trial
The co-administration study is a phase 3, open-label, multi-country study to assess non-inferiority of immune responses in co-administration of GSK’s RSV and Recombinant Zoster Vaccine (RZV) compared to separate administration in adults aged 50 and over.²

530 participants were randomized 1:1 to receive either GSK’s Recombinant Zoster Virus vaccine first dose and GSK’s Respiratory Syncytial Virus, Adjuvanted at visit one (Co-ad), or GSK’s Recombinant Zoster Virus vaccine first dose alone at visit one (Control). The Control group received GSK’s RSV vaccine at day 31.^1,2 RZV second dose was administered at day 61 for both groups.^1,2 The primary endpoint was the non-inferiority of the humoral immune responses to GSK’s RSV vaccine and RZV when co-administered compared to when administered at separate visits.^1,2 Key secondary endpoints included reactogenicity and safety following co-administration versus sequential administration of GSK’s RSV vaccine and RZV.^1,2

Anti-gE antibody concentrations and RSV-A and RSV-B neutralization titers increased from pre- to post-vaccination and met the non-inferiority criteria in the primary endpoint for the humoral immune responses to GSK’s RSV and shingles vaccines.² In both groups, the duration of solicited adverse events was short and comparable, and the most frequently reported adverse events were pain at the injection site, fatigue, and myalgia.² Unsolicited adverse events reporting rates were balanced between the co-administration and control groups.²

About RSV in Adults
RSV is a common, contagious respiratory virus affecting the lungs and breathing passages.³ Adults can be at increased risk for RSV disease due to certain underlying medical conditions, immune compromised status, or advanced age.³ RSV can exacerbate conditions, including COPD, asthma, and chronic heart failure and can lead to severe outcomes, such as pneumonia, hospitalization, and death.³

About Shingles
Shingles is caused by the reactivation of the varicella-zoster virus (VZV), the same virus that causes chickenpox.¹¹ By age 50, VZV is present in most adults¹² and may reactivate with advancing age.¹³ As people age, the strength of the immune system response to infection wanes, increasing the risk of developing shingles.¹¹ Shingles typically presents as a rash, with painful blisters across the chest, abdomen, or face.¹¹ The pain is often described as aching, burning, stabbing or shock-like.¹⁴ Following the rash, a person may experience post-herpetic neuralgia (PHN), a long-lasting nerve pain that can last weeks or months and occasionally persists for several years.¹⁴ PHN is the most common complication of shingles, occurring in 5–30% of all shingles cases from findings in various studies.¹⁵

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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References

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1. Clinicaltrials.gov, “A Study on Safety and Immune Response of Investigational RSV OA Vaccine in Combination With Herpes Zoster Vaccine in Healthy Adults (RSV-OA=ADJ-020)”, NCT05966090 – available at: https://clinicaltrials.gov/study/NCT05966090 - Accessed in September 2024.
2. Dennis P, et al. Co-administration of the adjuvanted respiratory syncytial virus (RSV) prefusion F protein vaccine (RSVPreF3 OA) with the adjuvanted recombinant zoster vaccine (RZV) in adults ≥50 years of age. Abstract presented at European Geriatric Medicine Society (EuGMS); 18–20 September 2024, Valencia, Spain.
3. Centers for Disease Control and Prevention (CDC), RSV in Adults. Available at: https://www.cdc.gov/rsv/older-adults/index.html. Last Accessed: September 2024.
4. Marra F, et al. Risk Factors for Herpes Zoster Infection: A Meta-Analysis. Open Forum Infect Dis 2020;7(1):ofaa005.
5. Chen S-Y, et al. Incidence of herpes zoster in patients with altered immune function. Infection. 2014; 42: 325–334
6. Falsey, AR et al. Respiratory syncytial virus infection in elderly and high-risk adults, in New Engl J Med 2005; 352:1749-59.
7. CDC. About Shingles (Herpes Zoster). Available at https://www.cdc.gov/shingles/about/index.html
8. CDC. Shingles (Herpes Zoster): Clinical Overview. Available at: https://www.cdc.gov/shingles/hcp/clinical-overview/index.html
9. Cunningham, AL, et al. Efficacy of the Herpes Zoster Subunit Vaccine in Adults 70 Years of Age or Older. New England Journal of Medicine. 2016;375(11):1019–32.
10. The GSK proprietary AS01 adjuvant system contains QS-21 Stimulon® adjuvant licensed from Antigenics LLC, a wholly owned subsidiary of Agenus Inc. (NASDAQ: AGEN), MPL and liposomes.
11. Harpaz R, et al. Advisory Committee on Immunization Practices (ACIP), Centers for Disease Control and Prevention (CDC). Prevention of herpes zoster: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2008;57(RR-5):1–30.
12. Johnson, R.W., et al. Herpes zoster epidemiology, management, and disease and economic burden in Europe: a multidisciplinary perspective. Therapeutic advances in vaccines. 2015;3(4):109–20.
13. Mueller, N.H., et al. Varicella zoster virus infection: clinical features, molecular pathogenesis of disease, and latency. Neurologic clinics. 2008;26(3):675–97.
14. Cheng J, Rosenquist RW. Herpes zoster and postherpetic neuralgia. Fundamentals of Pain Medicine. 2018:221-5.
15. Kawai K, Gebremeskel BG, Acosta CJ. Systematic review of incidence and complications of herpes zoster: towards a global perspective. BMJ Open. 2014;4:e004833. doi: 10.1136/bmjopen-2014-004833.

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FAQ

What were the results of GSK's phase 3 trial for AREXVY and SHINGRIX co-administration?

The trial met its primary endpoint, showing a non-inferior immune response when AREXVY (RSV vaccine) and SHINGRIX (shingles vaccine) were co-administered compared to separate administration in adults 50 years and older. The co-administration was well-tolerated with acceptable safety profiles.

What are the most common side effects reported in the GSK vaccine co-administration trial?

The most frequently reported adverse events in the trial were pain at the injection site, fatigue, and myalgia. The duration of these side effects was comparable between the co-administration and separate administration groups.

How might the results of GSK's vaccine co-administration study impact adult immunization?

The positive results from this study could potentially reduce barriers to adult immunization by decreasing the number of healthcare visits required for vaccination. This may help improve vaccination rates for RSV and shingles in adults.

What are GSK's next steps following the positive topline data for AREXVY and SHINGRIX co-administration?

GSK plans to submit the results for peer-reviewed scientific publication and use them to support regulatory submissions to the US FDA, European EMA, and other regulators. This could lead to expanded vaccine administration options in the future.