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Recce Pharmaceuticals (RCE) investor relations material
Recce Pharmaceuticals H2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Advanced lead anti-infective R327G into Phase 3 registrational trial for diabetic foot infections (DFI) in Indonesia, with interim analysis planned for accelerated approval in H1 2026.
Completed Phase II trial for ABSSSI, achieving 93% efficacy at day 14 and no serious adverse events, supporting further DFI patient enrolment.
Secured A$15.8 million in equity and A$11.5 million in non-dilutive debt, with an additional A$19 million available, ensuring a strong cash runway.
Awarded US$2 million grant from US Department of Defense for burn wound program and entered a research agreement with USAMRIID for biothreat pathogens.
Expanded global patent portfolio, with new patents granted in Australia, Japan, and China, extending protection beyond 2040.
Financial highlights
Total income of $7.7 million, primarily from R&D tax incentives and grants.
Operating loss increased to $21.4 million (2024: $17.7 million), mainly due to higher R&D expenditure.
Cash and cash equivalents at year-end: $10.4 million (2024: $4.4 million).
Net deficiency in equity of $3.1 million, improved from $9.5 million deficit in 2024.
No dividends declared or paid during the year.
Outlook and guidance
Indonesian Phase 3 DFI trial expected to conclude within 12 months, targeting regulatory approval and commercial launch in H1 2026.
Preparations underway for Phase 3 DFI trial in Australia to US FDA standards.
Phase II IV trial for UTI/urosepsis planned for FY26.
Ongoing expansion of manufacturing capacity and global commercial partnerships.
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