Highlights

  • $6.0 million institutional placement at 7.2 cents per share, led by Bell Potter.
  • FY26 revenue rose 42% to $15.8 million, with statutory NPAT of $1.5 million.
  • Preliminary fibrosis study showed an AUC of 0.820 for significant fibrosis.
  • FY27 guidance of $17 to $22 million revenue and $2.6 to $3.6 million EBITDA.

Resonance Health Ltd (ASX:RHT) has released a capital raising presentation for a $6.0 million institutional placement, along with preliminary results from its extended proof-of-concept (EPoC) liver fibrosis study. The placement is priced at 7.2 cents per share, and Bell Potter Securities is lead manager.

Placement Terms and Use of Funds

About 83.3 million new shares will be issued, representing 14.9% of enlarged capital. The price is a 12.2% discount to the last close of 8.2 cents. New shares are expected to be allotted on 9 November 2026, and no shareholder approval is required.

The funds will support MRI endpoint development ($1.2 million), expansion of the TrialsWest clinical trial network to the east coast ($1.5 million), the liver fibrosis device program ($1.5 million) and working capital ($1.4 million). Pro forma cash after the placement is $10.4 million.

FY26 Results and FY27 Guidance

Revenue for the year ended 30 June 2026 rose 42% to $15.8 million. Normalised EBITDA was $2.6 million, statutory NPAT was $1.5 million, and operating cash flow was positive in all four quarters.

For FY27, Resonance is guiding revenue of $17 to $22 million and EBITDA of $2.6 to $3.6 million. This guidance excludes fibrosis device revenue, acquisitions and new sites.

Preliminary Liver Fibrosis Results

An interim analysis of 50 of 68 enrolled subjects, from a single site in China, showed an AUC of 0.820 for significant fibrosis (F2 or above), with 75.0% sensitivity and 80.0% specificity. For advanced fibrosis (F3 or above), the AUC was 0.788.

The company noted the results are preliminary, have not been independently verified and come from a small cohort with wide confidence intervals. The device is investigational and is not cleared for clinical use. Next steps include completing the full study and an FDA Pre-Submission.

Key Takeaways

  • The $6.0 million placement strengthens Resonance's balance sheet for growth programs.
  • FY26 revenue growth was supported by all three business segments.
  • Early fibrosis results are encouraging but remain preliminary.
  • Key upcoming steps include the full EPoC analysis and FDA feedback.