UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 6-K
REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13a-16 OR
15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
For the
month of March 2026
Commission
File Number 001-15170
GSK plc
(Translation
of registrant's name into English)
79 New Oxford Street, London, WC1A 1DG
(Address
of principal executive office)
Indicate
by check mark whether the registrant files or will file annual
reports under cover of Form 20-F or Form 40-F.
Form
20-F . . . .X. . . . Form 40-F . . . . . . . .
Issued: 3 March 2026, London UK
GSK completes acquisition of RAPT Therapeutics
GSK plc (LSE/NYSE: GSK) today announced the completion of
its previously
announced acquisition
of RAPT Therapeutics, a California-based, clinical-stage
biopharmaceutical company dedicated to developing novel therapies
for patients living with inflammatory and immunologic
diseases.
The acquisition includes ozureprubart, a long-acting
anti-immunoglobulin E (IgE) monoclonal antibody, currently in phase
IIb clinical development for prophylactic protection against food
allergens. IgE is a clinically validated target and is the only
approved systemic therapy shown to protect patients from a harmful
allergic and inflammatory immune response. Around 94% of severe
food allergies are caused by IgE-mediated
reactions.1
Current anti-IgE treatment for food allergy involves injections
every 2 to 4 weeks, which can be a significant burden, particularly
since most patients are children. Ozureprubart's clinical profile
offers the potential for less frequent dosing of every 12 weeks,
supporting improved compliance and patient outcomes, as well as
providing a new option to approximately 25% of patients currently
ineligible for existing therapy. Ozureprubart complements GSK's
extensive commercial footprint and prescriber base in
allergy.
Data from the phase IIb trial (prestIgE) assessing use of
ozureprubart as monotherapy is expected in 2027, with phase III
trials to be focused on both at-risk adult and paediatric
populations.
Kaivan Khavandi, SVP, R&D Head Respiratory, Immunology &
Inflammation, and Head of GSK Translational & Development
Sciences, GSK said:
"Ozureprubart is a promising asset that complements our expanding
RI&I pipeline. Food allergies continue to place a heavy burden
on patients and their families, and we are committed to progressing
this potential best-in-class monoclonal antibody to deliver
longer-lasting protection."
Financial considerations
The total cash consideration for this acquisition amounts to an
approximate aggregate equity value of $2.2
billion. Net
of cash acquired, GSK's upfront investment is approximately $1.9
billion.
The transaction gives GSK the global rights to the ozureprubart
programme, excluding mainland China, Macau, Taiwan and Hong Kong.
GSK will also be responsible for success-based milestone and
royalty payments for ozureprubart owed to RAPT's partner, Shanghai
Jeyou Pharmaceutical Co., Ltd.
About food allergies
In the US, over 17 million people are diagnosed with food
allergies, with more than 1.3 million people suffering severe
reactions.2,3,4 Notably,
65% of severe food allergy patients are children and
adolescents.1 This
results in more than 3 million patient visits each year to hospital
and emergency care.5 Disease
burden is amplified by the frequency and complexity of allergic
reactions, which can escalate to anaphylaxis, emergency care and
impact a patient's wellbeing and participation in social
activities. Collectively, food allergies cost US families an
estimated $33 billion in 2024, underscoring the need for more
effective and durable therapies.5
About RAPT Therapeutics
RAPT Therapeutics is a clinical-stage immunology-based
biopharmaceutical company focused on discovering, developing and
commercializing novel therapies for patients living with
inflammatory and immunologic diseases. Utilizing deep and
proprietary expertise in immunology, RAPT develops novel molecules
that are designed to modulate the critical immune responses
underlying these diseases.
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.
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GSK enquiries
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Media:
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Tim Foley
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+44 (0) 20 8047 5502
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(London)
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Sarah Clements
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+44 (0) 20 8047 5502
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(London)
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Kathleen Quinn
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+1 202 603 5003
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(Washington DC)
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Lyndsay Meyer
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+1 202 302 4595
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(Washington DC)
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Investor Relations:
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Constantin Fest
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+44 (0) 7831 826525
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(London)
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James Dodwell
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+44 (0) 20 8047 2406
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(London)
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Mick Readey
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+44 (0) 7990 339653
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(London)
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Steph Mountifield
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+44 (0) 7796 707505
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(London)
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Jeff McLaughlin
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+1 215 751 7002
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(Philadelphia)
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Frannie DeFranco
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+1 215 751 3126
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(Philadelphia)
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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 in the "Risk
Factors" section in GSK's Annual Report on Form 20-F for 2024, and
GSK's Q4 Results for 2025.
Registered in England & Wales:
No.
3888792
Registered Office:
79
New Oxford Street
London
WC1A
1DG
References
1. GSK Epi assessment based on MarketScan and Optum claims
database
2. Warren CM, Aktas ON, Manalo LJ, Bartell TR, Gupta RS. The
epidemiology of multifood allergy in the United States: a
population-based study. Ann Allergy Asthma Immunol.
2023;130(5):637-648.e5.
3. US Census Bureau. Age and Sex, American Community Survey, ACS
1-Year Estimates Subject Tables, Table S0101, 2022. Accessed 9
January, 2026.
https://data.census.gov/table/ACSST1Y2022.S0101.
4. MarketScan's overall prevalence, and Optum's age-stratified
(<18; 18+) and overall prevalence. Severe FA defined as patients
with ER/inpatient visit or under specialist care.
5. FARE Food Allergy Facts and Statistics for the US (April
2024).
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf
by the undersigned, thereunto duly authorised.
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GSK plc
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(Registrant)
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Date: March
03, 2026
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By:/s/ VICTORIA
WHYTE
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Victoria Whyte
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Authorised
Signatory for and on
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behalf
of GSK plc
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