Recce Pharmaceuticals Receives Approval from Indonesia’s Drug and Food Authority for Registrational Phase 3 Trial of RECCE® 327 Topical Gel in Diabetic Foot Infections

In This Article:

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

  • Awarded expedited regulatory review status in Indonesia to fast-track progression of Phase 3 trial, bringing forward commercial opportunities in ASEAN region

SYDNEY, Dec. 10, 2024 (GLOBE NEWSWIRE) -- Recce Pharmaceuticals Ltd (ASX: RCE, FSE: R9Q), (Recce or the Company), the Company developing a new class of synthetic anti-infectives, today announced it has received approval from the Indonesian Drug and Food Regulatory Authority, Badan POM (BPOM), to initiate its registrational Phase 3 trial assessing RECCE® 327 as a topical gel (R327G) for the treatment of diabetic foot infections (DFIs).

This significant milestone follows the recent human ethics committee approval to commence patient dosing, underscoring Recce’s clinical research's alignment with regulatory and ethical standards within Indonesia. With both approvals now secured, the Company remains on track to commence the registrational Phase 3 trial this quarter.

These advancements are not only significant for the Company’s growth but also contribute positively to Indonesia's healthcare landscape by introducing potential novel treatments for infectious diseases, aligning with Recce’s commitment to addressing critical health challenges on an international scale.

“The approval of Recce Pharmaceuticals' Phase 3 clinical trial is an important advancement in expanding treatment options for diabetic foot infections in Indonesia,” said Taruna Ikrar, MD, Ph.D., Chairperson of the Indonesian Food and Drug Authority (BPOM). “BPOM is committed to fostering the timely development of innovative therapies to address urgent health challenges. This collaboration reflects Indonesia’s mission to enhance healthcare outcomes for its population, and we are eager to see the trial’s impact on patients requiring effective, novel anti-infective treatments.”

With over 19.5 million adults living with diabetes in Indonesia,1 the need for innovative therapies to address diabetes-related infections, such as foot infections, urinary tract infections, and surgical site infections, is urgent. As a Registrational Phase 3 clinical trial for DFIs, this is one of the largest DFI studies in the world,2 and the first of its kind across Indonesia.

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 (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 expected regulatory approval and commercial launch in H1 CY26.

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