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ASX: TLXTelix Pharmaceuticals LimitedHealth Care

Telix Q3 2026 Revenue US$245M, Up 19%

Telix reported Q3 2026 group revenue of US$245 million, up 19%, reaffirmed FY 2026 revenue and other income above US$1 billion and revised its R&D guidance.

By Digifin Pty Ltd · About this coverage

Key Points

  • Group revenue of US$245 million, up 19% on Q3 2025
  • Precision Medicine revenue of US$201 million, up 30%
  • FY 2026 revenue and other income expected to exceed US$1 billion
  • R&D guidance revised to US$240 million to US$260 million
  • FDA approved Pixclara for glioma imaging during the quarter
Telix Pharmaceuticals Limited (ASX:TLX)

About Telix (ASX:TLX)

Telix Pharmaceuticals Limited is an ASX-listed radiopharmaceutical company headquartered in Melbourne. It develops and commercialises precision diagnostics and targeted radiopharmaceutical therapies for cancer, with operations across North America, Europe, Latin America and Asia-Pacific.

Telix (ASX:TLX)'s third-quarter update shows revenue growth from its prostate cancer imaging products, reaffirms that FY 2026 revenue and other income is expected to exceed US$1 billion, and narrows R&D guidance.

Unaudited group revenue was US$245 million, up 19% on Q3 2025 and 1% lower than Q2 2026. Precision Medicine revenue, primarily Illuccix and Gozellix sales, was US$201 million, up 30%, while TMS third-party revenue fell 6% to US$44 million. U.S. dose volumes increased 1% quarter over quarter, which the CEO says reflects expected summer seasonality. Revenue is tracking in line with the upper end of FY 2026 guidance of US$950 million to US$970 million plus US$40 million of other income. R&D expenditure guidance is now US$240 million to US$260 million, previously US$230 million to US$270 million, subject to planned clinical, regulatory and development milestones. During the quarter the FDA approved Pixclara for glioma imaging, the BiPASS Phase 3 study completed enrollment of 350 patients, and Telix announced a merger with Isotope Technologies Munich SE (ITM).

The Zircaix BLA resubmission to the FDA is still being finalised, the Pixlumi application in Europe remains under review, and the OPTIMAL-PSMA data readout is not expected until the first half of 2027.

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Source: Telix Pharmaceuticals Limited (ASX:TLX), 21 October 2026. Summary content supplied by Digifin Pty Ltd.

News summary only, not financial advice. It does not consider your objectives, financial situation or needs.

Wednesday, 21 October 2026

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