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Mechanism-Driven Therapy
for Chronic Wound Healing

Mechanism Validated in Phase II Clinical Studies

CLINICALLY VALIDATED

Second Phase II

completed in venous leg ulcer patients, demonstrating effective debridement and accelerated healing

DUAL-ACTION MECHANISM

Heals + Debrides

continuous enzymatic debridement and activation of endogenous repair signalling

DESIGNED FOR CLINICAL USE

Practical

easy application, strong safety profile, and compatibility with standard care workflows

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Aurase Wound Gel

Our Solution

AURASE WOUND GEL

Aurase Wound Gel contains tarumase, a highly specific fibrinolytic enzyme cloned from maggot saliva

It is optimised for selective removal of devitalised tissue and formulated within a hydrogel for practical clinical use

Aurase Wound Gel is easy to apply and designed to integrate into standard wound care workflows without additional procedural burden or patient discomfort

It can be used at all stages of the wound healing journey, from early stage to wound closure, in all settings

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Key Characteristics of Aurase Wound Gel

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100% Standard of care fit

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Simple application during standard dressing changes

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Temperature stable: Ideal for community use

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Safe: No risk if left on wound; specificity & pH-dependent action spares healthy tissue

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Equally well suited to clinic & hospital environments

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High compatibility with established wound care products

Aurase Wound Gel is positioned to become the “go-to” first line healing & debridement therapy for all chronic wounds

MECHANISM OF ACTION

Actively heals: Activation of endogenous repair pathways (PAR2 receptors) involved in cell migration, proliferation, and tissue regeneration

Continuously debrides: Degrades fibrin anchors & co-opted fibrin for elastin & collagen

Optimises wound bed for healing: Hydrogel provides moist environment and  supports cell migration

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Aurase Wound Gel has completed its second Phase II clinical evaluation, validating its dual-action mechanism and demonstrating a substantial acceleration of healing compared with standard care

Full results will be reported in the forthcoming clinical study report

Proof-of-Concept

  • Tarumase successfully debrides wounds faster

  • More complete debridement & improved healing at increased enzyme concentrations

Strong Safety Profile

  • No indications of systemic absorption

  • No antibody generation

  • No systemic effects on coagulation

Pain-free

  • Does not add to patients’ already existing pain burden

  • No evidence of local tolerability issues

Development pipeline

Our Phase II trials explore debridement and healing in venous leg ulcers

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Get in touch with us

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Reductions Observed in Wound Area

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Increases in Granulation Tissue and Re-Epithelialised Area

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The darker central lines represent the mean and the shaded area represent the 95% confidence intervals

Debridement Efficiency: Reduction in Slough Content

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For more clinical evidence, see report from prior study

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