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Microba Life Sciences (MAP) Q4 2024 TU earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Microba Life Sciences Limited

Q4 2024 TU earnings summary

3 Feb, 2026

Executive summary

  • Achieved record full-year revenue of $12.09m, up 123% year-over-year, with Q4 revenue of $4.81m, up 20.2% quarter-over-quarter and 113% year-over-year.

  • Launched MetaPanel and MetaXplore diagnostic products, with strong adoption in Australia and expansion into the UK, and Invivo Clinical contributing $4.45m in H2 FY24 sales.

  • Advanced therapeutics pipeline, including completion of a world-first autoimmune discovery program with Ginkgo Bioworks, six promising leads, and preparation of MAP 315 for Phase 2 in IBD.

  • Ended Q4 with $20.9m in cash or equivalents, with ~$6m R&D tax incentive expected in H1 FY25.

  • Achieved ISO 15189 accreditation in Australia, CE marking in Europe, and CLIA/CAP in the US for non-diagnostic testing.

Financial highlights

  • Full-year revenue reached $12.09m, up 123% year-over-year; Q4 revenue was $4.81m, up 20.2% quarter-over-quarter and 113% year-over-year.

  • Core personal testing revenue was $4.61m, up 50% year-over-year.

  • Q4 cash receipts were $4.66m, up 15.7% quarter-over-quarter and 275.4% year-over-year; full-year cash receipts totaled $12.44m, up 148.1% year-over-year.

  • Invivo Clinical in the UK delivered $4.45m in H2 sales; Q4 sales were $2.21m.

  • Cash balance as of 30 June 2024 was $20.9m, with an additional ~$6m expected from the R&D tax incentive.

Outlook and guidance

  • Plans to launch MetaXplore in the UK in FY25, with expanded sales and marketing resources.

  • Focused on expanding reimbursement and coverage, especially in the US, and leveraging out-of-pocket payments in Australia and the UK.

  • Management anticipates continued growth, with meaningful sales volume and revenue growth expected from MetaPanel and MetaXplore expansion.

  • ~$6m R&D tax incentive expected in H1 FY25 to support operations.

  • No specific guidance yet on Phase 2 trial commencement for the lead therapeutic candidate.

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