CLINUVEL PHARMACEUTICALS LTD (ASX: CUV) reported in its Appendix 4E and Annual Report for the Australian financial year ended 30 June 2026 that revenue from ordinary activities decreased 1% to A$94.0 million, profit before tax fell 8% to A$47.7 million, and net profit attributable to members declined 6% to A$33.9 million, while the company remained debt free, increased cash reserves 12% to A$252.1 million, lifted net tangible assets per share to A$5.35, and declared a fully franked final dividend of A$0.05 per share with record date 4 September 2026 and payment date 18 September 2026; the report highlights a tenth consecutive annual profit and a strategy centred on North American expansion, continued growth of SCENESSE® for erythropoietic protoporphyria including Health Canada approval in July 2026, advancement of the Phase III vitiligo program with CUV105 completed and topline results planned for late 2026, progress on NEURACTHEL® and controlled-release peptide platform VLRX-L, expanded U.S. specialty centre and investor access initiatives including Nasdaq ADS trading from 20 July 2026, and consideration of a full Nasdaq listing and ASX delisting as part of a broader diversification plan to build multiple melanocortin-based revenue streams.
Key Points
Reporting period covers 1 July 2025 to 30 June 2026.
Revenue from ordinary activities decreased 1% to A$94,024,398.
Profit from ordinary activities before tax attributable to members decreased 8% to A$47,659,765.
Net profit for the period attributable to members decreased 6% to A$33,916,819.
A fully franked final dividend of A$0.05 per ordinary share was declared.
Dividend record date is 4 September 2026 and payment date is 18 September 2026.
Net tangible assets per security increased to A$5.35 from A$4.77.
SCENESSE® remained the company’s only approved therapy for EPP and doses administered rose to more than 21,000 implants.
North American specialty centres increased to 134, including 129 in the U.S. and 5 in Canada.
Health Canada granted a Notice of Compliance in July 2026 to market SCENESSE® for adult EPP patients in Canada.
The first Phase III vitiligo study CUV105 completed treatment and follow-up, with topline results planned for December 2026.
The second Phase III vitiligo study CUV107 was being designed with commencement targeted for late 2026.
NEURACTHEL® Instant manufacturing was validated and the first European regulatory submission is expected in the second half of 2026.
The VLRX-L controlled-release liquid peptide platform advanced into preclinical development.
PhotoCosmetics launch was deferred to 2027 to prioritise the vitiligo program.
CLINUVEL’s ADS uplift to Nasdaq Level II trading as CUVL commenced on 20 July 2026.
The company announced consideration of a full Nasdaq listing and delisting from the ASX.
IMPORTANT NOTE: This information is autogenerated and has not been reviewed for accuracy or completeness. You should refer to the full announcement here for further information.