GSK Plc current report, Q3 FY2026

Business Context and Reporting Period

Company: GSK plc
Filing Type: Form 6-K (Report of Foreign Private Issuer)
Reporting Period: Second Quarter (Q2) and Half-Year (H1) ended 30 June 2026
Announcement Date: 28 July 2026

GSK reported strong core performance driven by Specialty Medicines and Vaccines, offset by significant impairments in Total results. The company announced an "Accelerate Growth" programme to fund R&D investments and a new flagship R&D Centre in Cambridge, UK.

Key Financial Metrics (Q2 2026)

Metric Q2 2026 Value Q2 2025 Value Growth (CER%)
Turnover £8,409 million £7,986 million +5%
Total Operating Profit £481 million £2,023 million -75%
Total EPS 10.8p 35.5p -69%
Core Operating Profit £2,800 million £2,631 million +7%
Core EPS 50.5p 46.5p +9%
Cash from Operations £2,906 million £2,433 million +19%
Free Cash Flow £1,994 million £1,126 million +77%
Total Net Debt £15,132 million £13,735 million N/A

Material Changes vs. Prior Period

  • Revenue Growth: Total sales grew 5% at constant exchange rates (CER). Specialty Medicines sales increased 14% (HIV +10%, Oncology +17%, RI&I +19%). Vaccines sales rose 8% (Arexvy +>100%, Meningitis +21%). General Medicines declined 9% (Trelegy -7%).
  • Profitability Divergence: While Core Operating Profit grew 7%, Total Operating Profit fell 75% and Total EPS dropped 69%.
  • Impairments: The decline in Total results was primarily driven by a £1.3 billion impairment of camlipixant (following negative Phase III results) and a £371 million impairment related to the termination of assets under the Alector collaboration.
  • Other Adjusting Items: Higher Contingent Consideration Liability (CCL) charges and divestment income (linerixibat) impacted Total results.
  • Acquisitions: GSK completed acquisitions of RAPT Therapeutics and 35Pharma in Q1/Q2 2026. A post-balance sheet acquisition of Nuvalent Inc. closed on 15 July 2026 for approximately $10.6 billion.

Guidance, Outlook, and Management Commentary

2026 Guidance (Reaffirmed at CER)

  • Turnover: Increase of 3% to 5% (upper half of range).
  • Core Operating Profit: Increase of 7% to 9% (upper half of range).
  • Core EPS: Increase of 7% to 9% (lower half of range).

Strategic Initiatives

  • Accelerate Growth Programme: A 3-year initiative targeting £1.9 billion in annual savings by 2029 to fund late-stage R&D and improve margins during the dolutegravir loss of exclusivity period (2028-2030).
  • R&D Pipeline: Expectation of 20+ Phase III trial starts in 2026 (up from 10). Key assets include Jideytro (FDA approved), neladalkib (PDUFA H2 2026), and bepirovirsen (functional cure data positive).
  • Shareholder Returns: Q2 dividend of 17p declared; full-year 2026 dividend expected at 70p. Completed a £2 billion share buyback programme in June 2026.

Risks and Contingencies

  • Legal Matters: Ongoing Zantac litigation (summary judgment granted in Delaware, appeal filed); Avandia class certification vacated by Third Circuit; Zejula royalty dispute settled.
  • Regulatory: Agreement with US Government to lower prescription costs and exclude GSK/ViiV from Section 232 tariffs through 2029.
  • Geopolitical: Elevated risk regarding regulatory environment and trade policies.

Investor Verification Checklist

  • Impairment Details: Verify the specific recoverable amount calculations for camlipixant and the impact of the Alector collaboration termination on future R&D spend.
  • Nuvalent Acquisition: Review provisional accounting for the $10.6 billion Nuvalent acquisition (closed post-period) and its impact on Q3 2026 results and debt levels.
  • Accelerate Growth Savings: Monitor the realization of the targeted £1.9 billion annual savings and the associated restructuring costs in 2026-2027.
  • Contingent Consideration: Assess the sensitivity of the £6.78 billion contingent consideration liability to changes in sales forecasts and discount rates.
  • General Medicines Decline: Evaluate the trajectory of Trelegy sales given US Medicare benefit design changes and pricing pressures.