Investor presentation

On September 8, 2026 Integra Lifesciences presented its corporate presentation.

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(Presentation, Integra LifeSciences, SEP 8, 2026, View Source [SID1234670623])

HCW Biologics Entered an Exclusive Distribution Agreement with Akron Biotech to Commercialize HCW11-006 as Reagent Used to Support Production of Highly Functional Human CAR-T Cells

On September 8, 2026 HCW Biologics Inc. (the "Company" or "HCW Biologics") (NASDAQ: HCWB), a U.S.-based clinical-stage biopharmaceutical company focused on developing novel fusion immunotherapeutics to treat autoimmune diseases, cancer, and senescence-associated dysplasia, reported that the Company has entered into an Exclusive Distribution Agreement with Akron Biotech ("Akron"), a leading manufacturer of ancillary materials and a contract development and manufacturing organization for the cell, gene therapy, and regenerative medicine industries, for the commercialization of HCW11-006 for use as a reagent to support a new method of producing highly functional human CAR-T cells for treating cancer, autoimmune disease, and infectious diseases. Akron operates within a highly specialized global network of biomedical institutions, primarily catering to a customer base of advanced therapy developers, biopharmaceutical companies, and research organizations. Akron manufactures and markets cGMP-compliant ancillary materials (such as cytokines, media supplements, and plasmid DNA) necessary for bringing regenerative medicine from preclinical stages to commercialization.

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HCW11-006, a first-in-class multi-cytokine fusion molecule built with our proprietary TRBC platform, enables production of more potent CAR-T-based immunotherapies by generating a CAR-T population that is highly functional and markedly enriched for long-lived T-memory stem cells (Tscm). Utilizing HCW11-006 as part of a manufacturing strategy may be broadly applicable to increase persistence and functionality of CAR-Ts. Functional persistence of CAR-Ts is limited by conventional and costly manufacturing methods utilizing anti-CD3/CD28 (αCD3/28)/IL-2 stimulation, which generates terminally differentiated and shorter-lived CAR-Ts.

Utilizing HCW11-006 as a reagent in the manufacture of CAR-Ts synergizes the effects of IL-7, IL-15 and IL-21 to promote the generation of a CAR-T cell product with a diverse mix of T cell subsets that exhibit a combination of Tscm self-renewal capacity and enhanced T cell effector function. In addition, as a reagent, HCW11-006 stimulates proliferation of CD8+ T cells, particularly those within the Tscm subset. As a result, HCW11-006 was shown to generate CAR-Ts without requiring αCD3/28/IL-2 activation that are highly enriched in long-lived Tscm and display potent activity across distinct disease experimental models, namely, HIV-1 and B-cell leukemia.

In preclinical studies, CAR-Ts manufactured using HCW11-006 were significantly superior compared to CAR-Ts manufactured using standard methods employing αCD3/28/IL-2 reagents for CAR lentiviral transduction and subsequent expansion and persistence of highly active human CAR-Ts. Clinical studies are planned to further confirm these findings. This research suggests that CAR-T cells produced with HCW11-006 may be a more effective and longer-lasting CAR-T cell immunotherapy than conventional CAR-T cells produced using αCD3/28/IL-2.

Dr. Hing C. Wong, the Company’s Founder and Chief Executive Officer, stated, "We are thrilled that our first product, created using our proprietary TRBC platform, has reached the commercialization stage. HCW11-006 is a novel compound that enables a single molecule to deliver synergistic signals from three different immune-stimulatory cytokines. It is versatile and can be used as a novel reagent to potentially replace the current industry-standard method that relies on αCD3/28/IL-2-based approaches. An approach that employs HCW11-006 as a reagent is highly streamlined and may lower the cost of CAR-T manufacturing compared to existing approaches. Equally important, based on experimental models, HCW11-006 has shown improvement in functional activities and persistence of CAR-Ts following adoptive transfer, a goal the industry has been trying to achieve for the last decade."

Dr. Wong continued, "We are pleased to be entering into a partnership with Akron Biotech and their extensive network of customers who include leading research institutions all over the world that will include the use of CAR-T treatments produced using HCW11-006 as a reagent in clinical research and scale-up of commercialization. Recently, research laboratories and companies approached us directly seeking supply of HCW11-006 to support their cell-based research and development for their novel therapies. We decided to seek a partnership with a leading supplier to commercialize HCW11-006 for use as a reagent. We are excited to enter into this Distribution Agreement to commercialize this application of HCW11-006 as a reagent with an established firm that specializes in manufacturing and distribution of cell-based, gene and regenerative therapies."

Article Referenced in Press Release:

Cole et al., "IL-7/IL-15/IL-21 cytokine-fusion scaffold generates highly functional CAR T cells enriched in long-lived T memory stem cells," Science Advances, Vol. 12, No.11, 13 Mar 2026

(Press release, HCW Biologics, SEP 8, 2026, View Source [SID1234670622])

GSK delivers Q2 sales of £8.4 billion +5% AER, +5% CER

On September 8, 2026 GSK reported Q2 sales of £8.4 billion +5% AER, +5% CER.

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Recent Developments

Pipeline progress:


Two late-stage medicines for non-small cell lung cancer acquired: Jideytro (FDA approval) & neladalkib (PDUFA H2 2026)


Positive phase III Hansoh China data for Ris-Rez in lung cancer – first positive phase III overall survival data reported for a B7-H3 targeted ADC in any tumour type


Positive data (AZUR-1) supports regulatory reviews for use of Jemperli in treatment of advanced rectal cancer


Momelotinib (Ojjaara) granted Orphan Drug Designations in US and EU for VEXAS syndrome


Pivotal data demonstrates unprecedented functional cure rates for bepirovirsen (chronic hepatitis B)


Arexvy expanded approval in Japan for adults aged 18-59 at increased risk of RSV


Decision not to progress further development of camlipixant in RCC following CALM-1/2 phase III results

R&D acceleration:


62 assets in clinical development with opportunities for significant growth


7 asset accelerations – across 18 indications – identified in: Oncology, Respiratory, Hepatology & Vaccines


Now expect 20+ phase III trial starts in 2026 (previously 10)


New flagship R&D Centre to be established in Cambridge Biomedical Campus, UK


3-year programme to fund investment in late-stage portfolio and to improve operating margin with £1.9 billion annual savings targeted by 2029 for costs of £2.4 billion (£2.1 billion cash costs)

Agreement with US Government to lower the cost of prescription medicines for American patients

As previously announced, on 19 December 2025, GSK entered into an agreement with the US Administration to lower the cost of prescription medicines for American patients, which, once fully implemented, would exclude both GSK and ViiV Healthcare from Section 232 tariffs for three years. On 9 April 2026, GSK, ViiV Healthcare, and the US Government entered into a definitive agreement reflecting Section 232 tariff relief through 20 January 2029 (subject to final implementation). As part of that implementation, GSK and ViiV Healthcare each signed a Generous Model Manufacturer Participation Agreement with the Centers for Medicare and Medicaid Services effective 15 June 2026. With these agreements GSK and ViiV Healthcare have committed certain products to participate in the voluntary Generous Model, and it is anticipated that supplemental rebate agreements with interested US states will be signed on or before 1 October 2026.

Investing in late-stage product portfolio and Accelerate Growth programme

GSK has 62 assets in clinical development, 19 of which are in phase III development.

The company has strong confidence in its late-stage product portfolio, based on clinical data and the opportunities it has identified to improve upon current standards-of-care. GSK has potential best-in-class products for Oncology, Respiratory, Hepatology, HIV and Vaccines.

Following review, the company has identified asset accelerations – across 18 indications – for 7 late-stage products in Oncology, Respiratory, Hepatology and Vaccines. GSK now also expects to start 20+ phase III trials in 2026 (previously 10).

To accelerate R&D and capture the growth and value the late-stage portfolio offers, GSK has initiated a new "Accelerate Growth" programme. This 3-year programme has two objectives:

(1)
Simplify, and match GSK’s organisation and cost base to its evolving product portfolio, notably in Specialty Medicines

(2)
Enable the reallocation of GSK’s capital and resources to the late-stage pipeline and to R&D.

The Accelerate Growth programme is targeting £1.9 billion of annual savings, to be fully realised by 2029, for expected total costs of £2.4 billion, of which £2.1 billion is expected to be cash costs. Savings will be primarily reinvested in R&D, including business development activity, with a portion also used to strengthen operating margin in the period related to LoE for dolutegravir (2028-2030). The Accelerate Growth programme will be treated as a Major restructuring programme and costs will be included in Adjusting items. The majority of the cost charges will be in 2026 and 2027.

Cost savings are expected to be enabled by technology and AI and generated by streamlining support services and process redesign including procurement delivery, the reallocation of resources to Specialty Medicines from established products and further simplification of supply chain and the site network to align with portfolio evolution.

Dividend policy

The Dividend policy and the expected pay-out ratio remain unchanged. Consistent with this, GSK has declared a dividend for Q2 2026 of 17p per share. GSK’s future dividend policy and guidance regarding the expected dividend pay-out in 2026 are provided on page 41.

In Q2 2026, GSK completed the £2 billion share buyback programme announced in FY 2024.

Exchange rates

If exchange rates were to hold at the closing rates on 20 July 2026 ($1.35/£1, €1.18/£1 and Yen 219/£1) for the rest of 2026, the estimated impact on 2026 Sterling turnover growth for GSK would be -2%.

Performance : turnover

Turnover

Q2 2026 Year to date
£m AER% CER% £m AER% CER%
HIV

2,078 11 10 3,902 9 10
Respiratory, Immunology & Inflammation (RI&I)

1,135 18 19 2,025 15 17
Oncology

569 18 17 1,081 20 22
Specialty Medicines

  3,782 14 14 7,008 12 14
Shingles (Shingrix)

888 4 3 1,914 11 12
Meningitis

462 22 21 797 9 9
RSV (Arexvy)

192 >100 >100 257 78 75
Influenza

11 83 100 21 >100 >100
Other Paediatric & Adult Vaccines

731 (7 ) (8 ) 1,444 (9 ) (8 )
Vaccines

2,284 9 8 4,433 6 6
Respiratory

1,679 (10 ) (10 ) 3,273 (9 ) (7 )
Other General Medicines

664 (5 ) (4 ) 1,324 (10 ) (8 )
General Medicines

2,343 (9 ) (9 ) 4,597 (9 ) (7 )
Total

8,409 5 5 16,038 3 5
By Region:


US

4,308 5 5 8,045 2 6
Europe

2,042 11 8 4,125 15 11
International

2,059 1 2 3,868 (4 ) (2 )
Total

8,409 5 5 16,038 3 5

Financial Performance – Q2 2026 results unless otherwise stated, growth % and commentary at AER and CER. The YTD adverse currency impact on AER versus CER primarily reflected the strengthening of Sterling against the USD. See page 10 for further details.

For product list – see page 56

Q2 2026

Year to date Key Drivers
£m AER%

CER%

£m AER% CER%
 Specialty

 Medicines Total

3,782 14 14 7,008 12 14 Continued growth across disease areas, with strong performances in HIV, Respiratory, Immunology & Inflammation, and Oncology.
 HIV

2,078 11 10 3,902 9 10
In Q2 LAIs delivered 76% at AER, 80% at CER of total HIV growth. Strong demand for Cabenuva, Apretude and Dovato more than offset mature portfolio declines, with favourable pricing from US channel mix benefitting growth. US HIV sales increased in Q2 by 13% AER, 14% CER and YTD by 11% AER, 14% CER with LAIs representing 35% of US HIV turnover.

YTD LAI sales exceeded £1bn.

  Dovato

749 14 13 1,415 16 16 Strong demand across all regions.
  Cabenuva

453 33 33 821 29 32 Cabenuva contributed 57% at AER, 60% at CER of total HIV growth in Q2, with strong demand across all regions.
  Apretude

140 39 39 260 37 41 Strong growth driven by demand in a competitive US long-acting prevention market, contributing 20% at AER and CER of total HIV growth in Q2.
 RI&I

1,135 18 19 2,025 15 17 Growth driven by Nucala and Exdensur in respiratory and Benlysta in immunology.


Q2 2026 Year to date Key Drivers

£m AER% CER% £m AER% CER%
  Nucala

610 22 23 1,094 16 18
Strong demand across all regions and indications, enhanced by COPD launches including the US in Q2 2025. US grew double digit in the quarter and YTD with volume growth more than offsetting continued unfavourable pricing pressures. In Q2, US channel mix pricing adjustments positively impacted total growth in the quarter by 12 ppts and YTD by 6 ppts.

  Exdensur

18 – – 29 – –
Early commercial introductions across all launched markets, with new patient starts increasing in Q2 in key growth markets US, Japan and Germany.

  Benlysta

498 10 11 882 9 12
Strong volume growth in Q2 and YTD, with bio-penetration rates having increased across many markets.

 Oncology

569 18 17 1,081 20 22
Increasing patient demand for Jemperli, Ojjaara/Omjjara and Blenrep, partially offset by a decrease in Zejula.

  Jemperli

248 27 27 480 30 33
Continued strong growth in Q2 and YTD across all regions. US continued to grow double-digit, which reduced in Q2 as new patient starts moderated. Strong growth continued in Europe and International driven by launches and reimbursement expansion across markets.

  Ojjaara/Omjjara

187 36 36 331 32 35
Higher patient uptake across the regions and from continued commercial launches across Europe and International markets. US volume growth in Q2 and YTD was partly offset by continuing pricing pressures.

  Zejula

101 (33) (34) 215 (24) (23)
US continues to decline with volume impacted by the FDA label update and new prior authorisation insurance requirements, with Q2 further impacted by unfavourable channel mix and returns adjustments. Europe declined due to increased competition.

  Blenrep

36 >100 >100 59 >100 >100
US sales driven by patient uptake in both community and academic settings. Continued geographic expansion with regulatory approval and launches across Europe and International markets, including in Germany, Japan and Brazil.


Q2 2026 Year to date
Key Drivers


£m AER% CER% £m AER% CER%
Vaccines Total

2,284 9 8 4,433 6 6
Strong Q2 driven by growth in Arexvy, Meningitis vaccines and Shingrix. Growth in Q2 benefitted 3ppts from prior period rebate adjustments.

Shingrix

888 4 3 1,914 11 12
Q2 growth was driven by demand in Europe, partly

offset by lower sales in International. US sales were

broadly stable with lower demand and channel

inventory utilisation offset by favourable pricing

including prior period rebate adjustments which

added 2ppts at AER, 3ppts at CER to Shingrix Q2 growth.

The cumulative immunisation rate in the US reached 45%, up 3ppts compared to 12 months earlier(1). The majority of ex-US Shingrix opportunity is in 10 markets where the average immunisation rate is around 12%, with significantly higher uptake in funded cohorts.

Meningitis

462 22 21 797 9 9
Q2 growth was delivered primarily by Bexsero with

outbreak-related demand in International and

Europe. Other Meningitis vaccines benefitted from

Q2 tender deliveries in International and Penmenvy

continued post launch uptake in the US.

Arexvy

192 >100 >100 257 78 75
Strong growth in Q2 was the result of Australian

tender deliveries and prior period rebate adjustments

in the US. YTD growth also benefitted from

expanded funding and uptake in Europe.

Other Paediatric &

Adult Vaccines

731 (7) (8) 1,444 (9) (8)
Decrease in growth due to competitive pressure for Other Vaccines, particularly Synflorix in International and prior year CDC stockpile replenishment for Infanrix/Pediarix in the US, partly offset by favourable CDC stockpile movements and pricing for Boostrix in the US in 2026.

Second quarter 2026

LOGO

Q2 2026 Year to date
Key Drivers

£m AER% CER% £m AER% CER%
General

Medicines Total

2,343 (9) (9) 4,597 (9) (7)
Decreases in Trelegy, other Respiratory and Other General Medicines products.

Respiratory

1,679 (10) (10) 3,273 (9) (7)
Trelegy decreases driven by US Medicare benefit design changes, and continued pricing pressures including the impact of channel mix pricing adjustments. Decreases in other respiratory products due to continued competitive pressures and generic erosion.

Trelegy

775 (7) (7) 1,421 (6) (3)
US declined by 7% AER and CER in Q2 and by 6% AER, 3% CER in YTD with volumes adversely impacted by Medicare benefit design changes and continued unfavourable pricing pressures as well as channel mix pricing adjustments impacting growth in Q2 by 5 ppts and YTD by 4 ppts. Strong volume growth in Europe and International was driven by patient demand, SITT class growth and increased market share.

Other General

Medicines

664 (5) (4) 1,324 (10) (8)
Decrease in growth driven by continued competitive pressures and generic competition across the portfolio and a reduction in contract manufacturing sales.

By Region

Q2 2026 Year to date Key Drivers
£m AER% CER% £m AER% CER%
US

4,308 5 5 8,045 2 6
Specialty Medicines: Q2 +15% AER, +15% CER, YTD AER +12%, CER+16%

Growth driven largely by patient demand in HIV, Oncology, Benlysta and Nucala.

Vaccines: Q2 +9% AER, +9% CER, YTD -1% AER, CER+3% CER

Growth in Q2 and YTD driven by favourable CDC stockpile movements and pricing for Boostrix and prior period RAR adjustments for Arexvy, partly offset in the YTD at AER by exchange rate impacts.

General Medicines: Q2 -18% AER, -17% CER, YTD -15% AER, -12% CER

Trelegy declines from sales volume impacts and unfavourable pricing pressures and adjustments. Decreases continued across the other respiratory and Other General Medicine portfolios from ongoing competitive and pricing pressures.

Europe

2,042 11 8 4,125 15 11
Specialty Medicines: Q2 +12% AER, +9% CER, YTD +12% AER, +9% CER

Growth driven by Oncology, Nucala, Benlysta and HIV.

Vaccines: Q2 +16% AER, +13% CER, YTD +27% AER and +22% CER

Growth driven by Shingrix demand in the Nordics and Austria, with significant increased demand across Europe YTD. Bexsero also grew due to Meningitis B outbreak related demand in the UK.

General Medicines: Q2 +3% AER, stable CER, YTD +2% AER, -1% CER

Growth in Trelegy and Anoro offset by decreases in other respiratory products.

International

2,059 1 2 3,868 (4 ) (2 )
Specialty Medicines: Q2 +11% AER, +11% CER, YTD +11% AER, +13% CER

Growth driven by Oncology, Nucala and Benlysta.

Vaccines: Q2 +3% AER, +3% CER, YTD -8% AER, -7% CER

Q2 growth in Arexvy from Australian tender deliveries and Bexsero demand related to outbreaks in Vietnam partly offset by lower sales of Shingrix and competitive pressure for Other Vaccines, particularly Synflorix. YTD sales include the impact of lower Q1 Synflorix and Shingrix sales.

General Medicines: Q2 -4% AER, -2% CER, YTD -9% AER, -6% CER

Growth in Trelegy and Anoro more than offset by decreases across other respiratory and Other General Medicine products, which included reductions in contract manufacturing income.

Financial performance – Total results

Total operating profit decreased in the quarter primarily due to higher impairments and higher CCL charges as well as increased investment in R&D and new asset launches and lower royalty income, partly offset by higher turnover, favourable product and regional mix, favourable net legal settlements and expenses in Q1 2026, higher other net operating income and lower NCIs.

Total EPS decreased in Q2 2026 and YTD primarily due to lower Total operating profit driven by higher impairments in the quarter, partly offset by the share buyback, a lower effective tax rate and lower NCIs, as well as lower net finance expenses in Q2.


Total Results Q2 2026 Year to date

£m % AER % CER £m % AER % CER
Turnover

  8,409    5    5   16,038    3    5
Cost of sales

(2,266) 5 3 (4,141) 1 1
% of sales

26.9% (0.2) (0.5) 25.8% (0.6) (1.1)
Selling, general and administration

(2,202) 3 3 (4,321) 3 3
% of sales

26.2% (0.6) (0.5) 26.9% (0.2) (0.4)
Research and development

(3,466) 71 71 (5,158) 48 49
% of sales

41.2% 15.9 15.9 32.2% 9.7 9.5
Royalty income

204 (17) (17) 399 (6) (7)
Other operating income/(expense)

(198) >100 >100 (43) >100 >100
Operating profit

481 (76) (75) 2,774 (35) (31)
% of sales

5.7% (19.6) (19.3) 17.3% (10.0) (9.3)
Net finance expense

(124) (7) (7) (269) 11 13
Share of after tax profit/(loss) of associates

and joint ventures

(3) (7)
Profit before taxation

354 (81) (80) 2,498 (37) (34)
Taxation

199 >(100) >(100) (106) (82) (77)
Tax rate %

(56.2%) 4.2%
Profit after taxation

553 (66) (65) 2,392 (30) (26)
Profit attributable to non-controlling interests

118 (42) (41) 220 (37) (35)
Profit attributable to shareholders

435 2,172
553 (66) (65) 2,392 (30) (26)
Earnings per share

10.8p (69) (69) 54.1p (28) (24)
Financial Performance – Q2 2026 results unless otherwise stated, growth % and commentary at AER and CER.

In YTD, the adverse currency impact on AER versus CER primarily reflected the strengthening of Sterling against the USD. See page 10 for further details. Reconciliations between Total results and Core results Q2 2026, Q2 2025, H1 2026 and H1 2025 are set out on pages 23 and 26.

Total cost of sales as a percentage of sales decreased in the quarter and YTD primarily driven by favourable product and regional mix driven by higher specialty sales and the growth of higher margin Vaccines products, particularly Shingrix in Europe, as well as a favourable comparator due to supply chain optimisation charges incurred in Q2 2025, partly offset by impairments in the quarter.

   Q2 2026   Q2 2025   H1 2026   H1 2025  2025
Average rates:


US$/£

1.34 1.34 1.34 1.30 1.31
Euro/£

1.15 1.18 1.15 1.19 1.17
Yen/£

213 194 212 193 198
Period-end rates:


US$/£

1.32 1.37 1.32 1.37 1.35
Euro/£

1.16 1.17 1.16 1.17 1.15
Yen/£

215 198 215 198 211
In Q2 2026 and YTD, the adverse currency impact primarily reflected the strengthening of Sterling against the US Dollar, particularly in Q1 2026, as well as the Yen and emerging market currencies, partly offset by strengthening of the Euro. Exchange losses on the settlement of intercompany transactions had an adverse impact of one percentage point on Total and Core EPS in the YTD, and minimal impact in the quarter.Cash generation

Cash flow


  Q2 2026
£m


  Q2 2025
£m

  H1 2026
£m


  H1 2025
£m

Cash generated from operations (£m)

2,906 2,433 4,256 3,734

Total net cash inflow/(outflow) from operating activities (£m)

2,690 2,096 3,831 3,241

Free cash inflow/(outflow)* (£m)

1,994 1,126 2,809 1,823

Free cash flow growth (%)

77% >100% 54% >100%

Free cash flow conversion* (%)

>100% 78% >100% 59%

Long-term borrowings

13,947 15,304 13,947 15,304

Total net debt** (£m)

15,132 13,735 15,132 13,735

* Free cash flow and free cash flow conversion are defined on page 60. Free cash flow is analysed on page 14.

** Total net debt is defined on page 61. Net debt is analysed on page 14.

Q2 2026

Cash generated from operations for the quarter was £2,906 million (Q2 2025: £2,433 million). The increase reflected higher Core operating profit driven by higher turnover, favourable product and regional mix, partially offset by increased investment in R&D and new asset launches, as well as lower royalty income in the quarter. In addition there were favourable timing and movements on trade receivables and payables, partly offset by inventory build to support new product launches and adverse timing and movements on returns and rebates.

Total contingent consideration cash payments in the quarter were £378 million (Q2 2025: £333 million). £374 million (Q2 2025: £330 million) of these were recognised in cash flows from operating activities, including cash payments made to Shionogi & Co. Ltd ("Shionogi") of £348 million (Q2 2025: £319 million).

Free cash inflow was £1,994 million for the quarter (Q2 2025: £1,126 million). The increase was primarily driven by higher cash generated from operations, proceeds from the divestment of linerixibat and lower tax payments.

H1 2026

Cash generated from operating activities was £4,256 million (H1 2025: £3,734 million). The increase reflected higher Core operating profit driven by higher turnover, favourable product and regional mix, and favourable net legal settlements and expenses in Q1 2026 partially offset by increased investment in R&D and new asset launches, as well as lower royalty income in Q2 2026. In addition there were favourable timing and movements on trade receivables and the final cash settlement from CureVac, partly offset by exchange and adverse timing and movements on returns and rebates.

Total contingent consideration cash payments in H1 2026 were £757 million (H1 2025: £674 million). £749 million (H1 2025: £668 million) of these were recognised in cash flows from operating activities, including cash payments made to Shionogi & Co. Ltd of £710 million (H1 2025: £650 million).

Free cash inflow was £2,809 million for H1 2026 (H1 2025: £1,823 million). The increase was driven by higher cash generated from operations, higher proceeds from the sale of intangible assets, including the divestment of linerixibat, and the special dividend of $250 million (£187 million) related to the ViiV shareholding restructure.

Total Net debt

At 30 June 2026, net debt was £15,132 million, compared with £14,453 million at 31 December 2025, comprising gross debt of £18,238 million and cash and liquid investments of £3,106 million. See net debt information on page 14.

Net debt increased by £679 million primarily due to net acquisition costs of £2,083 million related to RAPT Therapeutics and 35Pharma Inc., dividends paid to shareholders of £1,370 million, shares purchased as part of the share buyback programme (completed in June 2026) of £634 million and an exchange loss on net debt of £76 million. This was partly offset by primarily the free cash inflow of £2,809 million and £398 million related to the disposal of the Rockville site including proceeds and a reduction in lease liabilities.

Q2 2026 pipeline highlights (since 29 April 2026)

Medicine/vaccine Trial (indication, presentation) Event
Regulatory approvals or

other regulatory actions

Nucala Hypereosinophilic Syndrome Regulatory approval (CN)
Jideytro Non-small cell lung cancer (pre-treated) Regulatory approval (US)
Arexvy RSV, adults aged 18-49 years at increased risk Regulatory approval (JP)
Arexvy RSV, adults aged 18+ immunocompromised Regulatory approval (JP)
Utebzi PIVOT-PO (complicated urinary tract infections) Regulatory approval (US)
Regulatory submissions or acceptances Bexsero Meningococcal B booster (10+ years of age) Regulatory acceptance (EU)
Phase III data readouts or

other significant events

camlipixant* CALM-1/2 (refractory chronic cough) Phase III data readout
efimosfermin ZENITH-1 and ZENITH-2 (metabolic dysfunction-associated steatohepatitis) Breakthrough Designation (CN)
Jemperli AZUR-1 (rectal cancer) Positive phase II (pivotal) data readout
momelotinib VEXAS syndrome Orphan Drug Designation (EU, US)
*camlipixant demonstrated limited efficacy in the CALM-1 and CALM-2 pivotal trials, and, based on the aggregate data, GSK has decided not to progress further development in chronic cough (disclosed 17 July 2026)

Anticipated pipeline milestones

Timing

Medicine/vaccine Trial (indication, presentation) Event
H2 2026

Exdensur OCEAN (eosinophilic granulomatosis with polyangiitis) Phase III data readout
Ventolin Low carbon MDI (asthma) Regulatory submission (EU)
Blenrep DREAMM-8 (2L + multiple myeloma) Regulatory submission (CN)
Jemperli AZUR-1 (rectal cancer) Regulatory submission (US)
Jemperli AZUR-1 (rectal cancer) Regulatory decision (US)
neladalkib Non-small cell lung cancer (pre-treated) Regulatory decision (US)
cabotegravir 3x a year prevention (HIV) Phase IIb (pivotal) data readout
cabotegravir 3x a year prevention (HIV) Regulatory submission (US)
Arexvy RSV, adults aged 18+ immunocompromised Regulatory decision (US)
bepirovirsen B-WELL 1/2 (hepatitis B virus) Regulatory decision (US, JP)
Bexsero Meningococcal B (infants) Regulatory submission (US)
H1 2027

Exdensur OCEAN (eosinophilic granulomatosis with polyangiitis) Regulatory submission (US, EU, CN, JP)
Ventolin Low carbon MDI (asthma) Regulatory decision (EU)
Ventolin Low carbon MDI (asthma) Regulatory submission (US)
Jemperli AZUR-1 (rectal cancer) Regulatory submission (JP)
Jideytro Non-small cell lung cancer (treatment naïve) Regulatory submission (US)
cabotegravir 3x a year prevention (HIV) Regulatory decision (US)
Arexvy RSV, adults aged 60+ Regulatory decision (CN)
bepirovirsen B-WELL 1/2 (chronic hepatitis B) Regulatory decision (EU, CN)
H2 2027

Exdensur OCEAN (eosinophilic granulomatosis with polyangiitis) Regulatory decision (US, JP)
Jemperli AZUR-1 (rectal cancer) Regulatory submission (EU, CN)
Jemperli AZUR-1 (rectal cancer) Regulatory decision (EU)
zidesamtinib Non-small cell lung cancer (treatment naïve) Regulatory decision (US)
cabotegravir + rilpivirine CUATRO, 3x a year treatment (HIV) Phase III data readout
Arexvy RSV, adults aged 18-59 Regulatory submission (CN)
Bexsero Meningococcal B (infants) Regulatory decision (US)

Progress on areas for responsible business

Being a responsible business is a fundamental part of GSK’s strategy and supports long-term performance. Annual progress against GSK’s responsible business priorities is detailed in the Annual(1) and Responsible Business(2) Reports with incremental updates shared each quarter. Highlights below include activity since Q1 2026 results.

Access


In April, GSK and Medicines for Malaria Venture (MMV) announced(3) the world’s first rollout of paediatric tafenoquine in Brazil – followed by Thailand in May – providing children with relapsing P. Vivax malaria access to this single dose treatment to help prevent relapse and support elimination efforts.

Global health and health security


Malaria remains one of the leading causes of death among children under five in sub-Saharan Africa. In May, results published(4) in The Lancet from the World Health Organization’s Malaria Vaccine Implementation Programme (MVIP), provided real-world evidence that the RTS,S malaria vaccine, developed by GSK, helped reduce child mortality over a period of four years in Ghana, Kenya and Malawi, with an estimated one in eight deaths averted among eligible children.


In July, the GSK-developed novel M72/AS01E tuberculosis vaccine candidate (licensed to Gates Medical Research Institute in 2020) progressed(5) toward global access with a new manufacturing agreement between the Gates MRI and Serum Institute of India, pending successful Phase III trial outcomes. The agreement also commits GSK, as the adjuvant innovator, to a manufacturing partner for M72/ AS01E, and marks a critical step toward ensuring that, if approved, the vaccine can be produced at scale and made available to those who need it most.

Environment


In May, GSK was named a Supplier Engagement Leader by the CDP(6), in addition to maintaining A-list status for Climate Change and Water Security. This recognises GSK’s work with suppliers to decarbonise its value chain beyond its own operations, which protects supply chain resilience and long-term ability to deliver medicines and vaccines.

Responsible Business rating performance

Detailed below is how GSK performs in key Responsible Business ratings*.

External benchmark

Current
score/ranking

Previous
score/ranking

Comments
Access to Medicines Index

3.72 4.06 Second in the Index, updated bi-annually, current results from November 2024. Scores range from 1 to 5, with 5 being the highest (best) score
Antimicrobial resistance benchmark

77% 84% Led the benchmark since its inception in 2018; Current ranking updated March 2026
CDP Climate Change

A A Updated annually, current scores updated December 2025 (for supplier engagement, May 2026)
CDP Water Security

A A
CDP supplier engagement rating Leader Leader
Sustainalytics

Low risk Low risk 2nd percentile in pharma subindustry group. Current rating as at July 2026
ISS Corporate Rating

B+ B+ Ranked 1st in our peer group. Last profile update May 2026
FTSE4Good

Member Member Member since 2004, latest review in July 2026

Total and Core results

Total reported results represent the Group’s overall performance.

GSK uses a number of non-IFRS measures to report the performance of its business. Core results and other non-IFRS measures may be considered in addition to, but not as a substitute for, or superior to, information presented in accordance with IFRS. Core results are defined below and other non-IFRS measures are defined on pages 60 and 61.

GSK believes that Core results, when considered together with Total results, provide investors, analysts and other stakeholders with helpful complementary information to understand better the financial performance and position of the Group from period to period, and allow the Group’s performance to be more easily compared against the majority of its peer companies. These measures are also used by management for planning and reporting purposes. They may not be directly comparable with similarly described measures used by other companies.

GSK encourages investors and analysts not to rely on any single financial measure but to review GSK’s quarterly results announcements, including the financial statements and notes, in their entirety.

GSK is committed to continuously improving its financial reporting, in line with evolving regulatory requirements and best practice. In line with this practice, GSK expects to continue to review and refine its reporting framework.

Core results exclude the following items in relation to our operations from Total results, together with the tax effects of all of these items:


amortisation of intangible assets (excluding computer software and capitalised development costs) to reflect the Group’s performance excluding the effect of acquisitions


impairment of intangible assets (excluding computer software) and goodwill to reflect the Group’s performance excluding the effect of acquisitions


major restructuring and integration costs, which are:


cash and non-cash costs such as impairment of tangible assets and computer software of Major restructuring programmes, which are specific Board-approved programmes that are structural and of significant scale, where the costs of individual or related projects within such programmes exceed £25 million; or


costs that relate to restructuring and integration following a significant acquisition.


Costs for other ordinary course, smaller-scale restructuring and integration are retained within both Total and Core results


transaction-related accounting or other adjustments related to significant acquisitions


proceeds and costs of disposal of associates, products and businesses; significant settlement income; Significant legal charges (net of insurance recoveries) and expenses on the settlement of litigation and government investigations; other operating income other than royalty income, and other items including amounts reclassified from the foreign currency translation reserve to the income statement upon the liquidation of a subsidiary where the amount exceeds £25 million

As Core results include the benefits of Major restructuring programmes but exclude significant costs (such as Significant legal charges and expenses, major restructuring costs and transaction items) they should not be regarded as a complete picture of the Group’s financial performance, which is presented in Total results. The exclusion of other Adjusting items may result in Core earnings being materially higher or lower than Total earnings. In particular, when significant impairments, restructuring charges and legal costs are excluded, Core earnings will be higher than Total earnings.

GSK has undertaken a number of Major restructuring programmes in response to significant changes in the Group’s trading environment or overall strategy or following material acquisitions. Within the Pharmaceuticals sector, the highly regulated manufacturing operations and supply chains and long lifecycle of the business mean that restructuring programmes, particularly those that involve the rationalisation or closure of manufacturing or R&D sites are likely to take several years to complete. Costs, both cash and non-cash, of these programmes are provided for as individual elements are approved and meet the accounting recognition criteria. As a result, charges may be incurred over a number of years following the initiation of a Major restructuring programme.

Significant legal charges and expenses are those arising from the settlement of litigation or government investigations that are not in the normal course and materially larger than more regularly occurring individual matters. They also include certain major legacy matters.

Reconciliations between Total and Core results, providing further information on the key Adjusting items, are set out on pages 23 and 26.

GSK provides earnings guidance to the investor community on the basis of Core results. This is in line with peer companies and expectations of the investor community, supporting easier comparison of the Group’s performance with its peers. GSK is not able to give guidance for Total results as it cannot reliably forecast certain material elements of the Total results, particularly the future fair value movements on contingent consideration and put options that can and have given rise to significant adjustments driven by external factors such as currency and other movements in capital markets.

(Press release, GlaxoSmithKline, SEP 8, 2026, View Source [SID1234670621])

Genprex to Present at the H.C. Wainwright 28th Annual Global Investment Conference

On September 8, 2026 Genprex, Inc. ("Genprex" or the "Company") (NASDAQ: GNPX), reported that members of its executive leadership team will present at and participate in the H.C. Wainwright 28th Annual Global Investment Conference, being held September 14–16 in New York City. Genprex is a clinical-stage biotechnology company developing gene therapies designed to restore tumor-suppressor function in cancer and insulin-producing function in diabetes. The Company’s lead oncology program is in clinical development, and its diabetes program is advancing through preclinical development.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Ryan Confer, Genprex’s President and Chief Executive Officer, will provide an overview of Reqorsa Gene Therapy, the Company’s lead clinical oncology candidate, and its preclinical diabetes program. He will also discuss the development priorities for each program.

Mark Berger, MD, Genprex’s Chief Medical Officer, and Thomas Gallagher, Genprex’s Senior Vice President of Intellectual Property and Licensing, will also attend the conference and participate in one-on-one investor meetings.

Company Presentation Details:

Date: Monday, September 14, 2026

Time: 3:30-4 p.m. ET

Location: Lotte New York Palace Hotel, Holmes I (4th Floor), New York, NY

Registered attendees may request one-on-one meetings with Genprex management via H.C. Wainwright.

(Press release, Genprex, SEP 8, 2026, https://www.genprex.com/2026/09/08/genprex-to-present-at-the-h-c-wainwright-28th-annual-global-investment-conference/ [SID1234670620])

Can-Fite Reports Q2 2026 Financial Results and Ongoing Clinical Progress Highlighting Longer-Than-Anticipated Overall Survival in Ongoing Pivotal Phase III Liver Cancer Study

On September 8, 2026 Can-Fite BioPharma Ltd. (NYSE American: CANF) (TASE: CANF), a biotechnology company developing a pipeline of proprietary small molecule drugs targeting oncological and inflammatory diseases, reported clinical updates and financial results for H1 2026.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Advances in Clinical Programs

Pancreatic Cancer
Phase 2a study evaluating Namodenoson in patients with advanced pancreatic ductal adenocarcinoma achieved its primary safety endpoint and demonstrated durable overall survival outcomes. The open-label Phase IIa study enrolled 20 patients with advanced pancreatic ductal adenocarcinoma who had progressed following standard therapies. Fourteen patients received Namodenoson as third-line treatment, five as second-line treatment, and one as fourth-line treatment. Namodenoson was well tolerated. Overall survival findings identify a subset of heavily pretreated pancreatic cancer patients achieving prolonged survival despite receiving Namodenoson as third-line therapy. A Phase IIb study protocol which combines chemotherapy and Namodenoson is under development. An abstract highlighting the positive results has been accepted for poster presentation at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress 2026.

Hepatocellular Carcinoma (HCC)
Blinded overall survival observed across the entire patient population in the Company’s ongoing pivotal Phase III study of Namodenoson in advanced hepatocellular carcinoma (HCC) appears longer than originally anticipated based on the assumptions underlying the study design.

In view of the longer-than-anticipated survival observed in the study population, Can-Fite is evaluating an earlier timing for the study’s planned interim analysis.

Clinical Progress in Psoriasis
The Company completed enrolment of the first 247 patients in its pivotal Phase 3 study evaluating Piclidenoson for the treatment of moderate-to-severe plaque psoriasis. The study has now reached the pre-specified interim analysis stage under a protocol agreed with both the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). The interim analysis will evaluate efficacy and safety data from the enrolled patients. Results are expected during Q1 2027.

Strengthening of Intellectual Property Portfolio
Can-Fite continued to expand its global intellectual property estate with multiple patent allowances across key territories, including Israel, Canada, Brazil, Australia and Japan, covering novel therapeutic uses of Namodenoson and Piclidenoson. These additions further strengthen the Company’s long-term commercial positioning and pipeline value.

Motti Farbstein Can-Fite’s CEO&CFO stated: "The first half of 2026 was marked by meaningful progress across our clinical programs. We are particularly encouraged by the longer-than-anticipated overall survival observed to date in our ongoing pivotal Phase III liver cancer study, while recognizing that the study remains blinded. In parallel, the durable survival outcomes observed in heavily pretreated pancreatic cancer patients and the advancement of our pivotal psoriasis study to its interim analysis stage further strengthen our clinical pipeline. We remain focused on disciplined execution of these late-stage programs and on advancing Namodenoson and Piclidenoson toward important clinical and regulatory milestones."

Financial Results

Revenues

Revenues for the six months ended June 30, 2026 were $0.20 million compared to $0.20 million for the six months ended June 30, 2025. Revenues for the six months ended June 30, 2026 and for the six months ended June 30, 2026 comprise of a portion of advance payments received under our existing out-licensing agreements with Cipher, CKD Gebro and Ewopharma.

Research and development expenses

Research and development expenses for the six months ended June 30, 2026 were $3.45 million, an increase of $0.42 million, or 13.86%, compared to $3.03 million for the six months ended June 30, 2025. Research and development expenses for the first half of 2026 comprised primarily of expenses associated with the ongoing of the Phase 3 study of Piclidenoson for the treatment of psoriasis and two ongoing studies for Namodenoson, a Phase 3 study in the treatment of advanced liver cancer and a Phase 2b study for MASH. The increase is primarily due to acceleration in expenses associated with both the Namodenoson and Piclidenoson programs.

General and administrative expenses

General and administrative expenses for the six months ended June 30, 2026 were $1.42 million, a decrease of $0.65 million, or 31.40%, compared to $2.07 million for the six months ended June 30, 2025. The decrease is primarily due to lower investors relations expenses. We expect that general and administrative expenses will remain at the same level through 2026.

Financial income, net

Financial income, net for the six months ended June 30, 2026 was $0.08 million compared to $0.02 million for the six months ended June 30, 2025. The increase in financial income, net was mainly due to higher interest income from bank deposits.

Net loss for the six months period ended June 30, 2026 was $4.60 million compared with a net loss of $4.87 million for the six months period ended June 30, 2025 . The decrease in net loss for the six months period ended June 30, 2026 was primarily attributable to a decrease in general and administrative expenses which was offset by an increase in research and development expenses .

As of June 30, 2026, Can-Fite had cash and cash equivalents and short term deposits of $7.03 million as compared to $8.53 million at December 31, 2025. The decrease in cash during the six months period ended June 30, 2026 is mainly due to the Company’s operating loss which was offset by proceeds from issuance of shares and warrants. During September 2026, the Company received aggregate gross proceeds of approximately $4.0 million from warrant exercises and a warrant inducement.

The Company’s consolidated financial results for the six months period ended June 30, 2026 are presented in accordance with US GAAP Reporting Standards.

CONDENSED CONSOLIDATED BALANCE SHEETS
U.S. dollars in thousands (except for share and per share data)
June 30, December 31,
2026 2025
Unaudited
ASSETS
CURRENT ASSETS:
Cash and cash equivalents $ 2,985 $ 5,528
Short term deposits 4,052 3,011
Prepaid expenses and other current assets 960 900
Short-term investment 6 1
Total current assets 8,003 9,440
NON-CURRENT ASSETS:
Operating lease right of use assets 47 69
Property, plant and equipment, net 5 5
Total non-current assets 52 74
Total assets $ 8,055 $ 9,514

CONDENSED CONSOLIDATED BALANCE SHEETS
U.S. dollars in thousands (except for share and per share data)
June 30, December 31,
2026 2025
Unaudited
LIABILITIES AND SHAREHOLDERS’ EQUITY
CURRENT LIABILITIES:
Trade payables $ 681 $ 1,161
Current maturity of operating lease liability 48 56
Deferred revenues 405 405
Other accounts payable 1,091 1,109
Total current liabilities 2,225 2,731
NON-CURRENT LIABILITIES:
Long – term operating lease liability 1 15
Deferred revenues 974 1,176
Total long-term liabilities 975 1,191
CONTINGENT LIABILITIES AND COMMITMENTS
SHAREHOLDERS’ EQUITY:
Ordinary shares of no-par value – Authorized: 30,000,000 and 14,000,000 shares at June 30, 2026 and December 31, 2025, respectively; Issued and outstanding: 4,285,093 and 2,618,425 shares as of June 30, 2026 and December 31, 2025, respectively - -
Additional paid-in capital 184,518 180,654
Accumulated other comprehensive income 1,127 1,127
Accumulated deficit (180,790 ) (176,189 )
Total shareholders’ equity 4,855 5,592
Total liabilities and shareholders’ equity $ 8,055 $ 9,514

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
U.S. dollars in thousands (except for share and per share data)
Six months ended
June 30,
2026 2025
Unaudited
Revenues $ 202 $ 202
Research and development expenses (3,456 ) (3,034 )
General and administrative expenses (1,426 ) (2,066 )
Operating loss (4,680 ) (4,898 )
Financial income, net 79 22
Operating loss (4,601 ) (4,876 )
Basic and diluted net loss per share (1.24 ) (4.29 )
Weighted average number of ordinary shares used in computing basic and diluted net loss per share 3,711,018 1,137,303

(Press release, Can-Fite BioPharma, SEP 8, 2026, View Source [SID1234670619])