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Recce Pharmaceuticals Receives Ethics Approval in Indonesia to Commence Registrational Phase 3 Trial of RECCE® 327 Topical Gel in Diabetic Foot Infections

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Recce Pharmaceuticals
Recce Pharmaceuticals
  • Human Research Ethics Committee approval received for registrational Phase 3 trial for RECCE® 327 topical gel in patients with diabetic foot infections

  • Registrational Phase 3 clinical trial for diabetic foot infections to be conducted across Indonesia, one of the world's largest diabetes patient populations

  • Data read-out and regulatory submission expected in late 2025 with potential approval and commercial launch in H1 2026

  • Bilateral initiative supported by Australian and Indonesian governments with clinical support from leading Indonesian biopharmaceutical company PT Etana Biotechnologies

SYDNEY, Nov. 12, 2024 (GLOBE NEWSWIRE) -- Recce Pharmaceuticals Ltd (ASX:RCE, FSE:R9Q), (the Company), the Company developing a new class of synthetic anti-infectives, today announced it received Human Research Ethics Committee approval to commence a registrational Phase 3 trial of RECCE® 327 as a topical gel (R327G) for the treatment of diabetic foot infections (DFI). Ethics approval signifies that Recce has met the safety and efficacy testing required to proceed with this large-scale, late-stage clinical trial.

“Today marks the achievement of a landmark milestone in Recce’s clinical program development,” said James Graham, Chief Executive Officer of Recce Pharmaceuticals. “We are thankful for the unparalleled support from our Indonesian partners in bringing our innovative anti-infective therapy to patients in need. This welcomed approval signals the beginning of our clinical programs in Indonesia and the broader ASEAN region, bringing Recce one step closer to commercialization. We look forward to evaluating R327G in our first Phase 3 trial.”

The trial will be conducted as a double-blinded, placebo-controlled study evaluating R327G for the treatment of DFIs and is on track to begin mid-December and aims to enroll up to 300 patients, with 200 to receive R327G and 100 to receive placebo. The trial will run for approximately 12 months, with an expected read-out in late 2025 and regulatory approval and commercial launch in H1 2026.

The study is made possible thanks to the significant support of key Indonesian stakeholders, including the Indonesian Ministry of Health, Badan POM, PT Etana Biotechnologies, and the Australian government, accelerating R327G’s path to commercialization. The study will cost Recce around $2M before further subsiding by the Australian government’s 43.5% R&D rebate scheme under the Company’s Advanced Overseas Advanced Finding status with AusIndustry. All intellectual property is that of Recce.

Indonesia’s clinical trial approval process involves two key steps: ethics approval (now approved) and BPOM (expected to follow imminently). Completing this trial would enable Recce to replicate regulatory approval for R327G across the broader ASEAN region, including Malaysia, the Philippines, Singapore, and Thailand, as a treatment for DFIs, addressing a critical unmet need for new therapeutics in countries facing increasing rates of antimicrobial resistance and infectious diseases.