Product image of Iruxol Mono (Collagenase Clostridium Histolyticum, Protease) supplied by GNH India

Iruxol Mono

Active Ingredient:
Collagenase Clostridium Histolyticum, Protease
Origin:
EU

Iruxol Mono (Collagenase Clostridium Histolyticum, Protease)

Collagenase Clostridium Histolyticum, Protease, the active ingredient in Iruxol Mono, is a collagenase enzyme presented as a topical formulation for skin application. It facilitates enzymatic debridement of necrotic tissue and supports remodeling of cutaneous wounds in patients with chronic or acute skin injuries.

GNH India supplies Iruxol Mono as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Smith & Nephew Gmbh

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Indications & Clinical Uses

Iruxol Mono is a topical collagenase used in the management of wounds that require enzymatic debridement.

  • Chronic venous leg ulcers: promotes removal of necrotic tissue to enhance healing.
  • Diabetic foot ulcers: assists in debridement of devitalized tissue, facilitating wound closure.
  • Pressure injuries (stage II–III): facilitates enzymatic debridement of damaged skin and underlying tissue.

How It Works

  • Collagenase Clostridium Histolyticum enzymatically cleaves native collagen fibers and other extracellular matrix proteins within necrotic tissue. By hydrolyzing peptide bonds in the triple‑helical structure of collagen, the enzyme breaks down the structural scaffold, allowing removal of devitalized tissue and promoting a healthier wound bed for subsequent regeneration.

Side Effects

Topical application of Iruxol Mono may be associated with local skin reactions and, rarely, systemic effects.

Common Side Effects

  • Redness at application site: mild erythema may appear.
  • Local pain or burning: transient discomfort during or after use.
  • Itching: occasional pruritus around treated area.
  • Swelling: mild edema may develop.

Serious or Rare Side Effects

  • Allergic reaction: hives, swelling, or rash indicating hypersensitivity.
  • Severe skin necrosis: excessive tissue breakdown beyond intended debridement.
  • Systemic hypersensitivity: anaphylaxis or severe systemic allergic response.

Precautions & Warnings

Precautions should be observed to minimize adverse outcomes.

  • Assess wound suitability: confirm presence of necrotic tissue before application.
  • Avoid healthy skin: do not apply to intact epidermis.
  • Infected wounds: use only under physician supervision when infection is present.
  • Monitor for allergic response: discontinue if signs of hypersensitivity appear.
  • Known hypersensitivity: avoid in patients with documented allergy to collagenase or protease enzymes.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Potential drug interactions may affect safety or efficacy.

Major Interactions (Avoid)

  • Concurrent topical proteolytic enzymes: may cause excessive tissue breakdown.
  • Systemic anticoagulants: increased risk of bleeding at the wound site.

Moderate Interactions (Monitor Closely)

  • Topical antibiotics: may alter local microbiome and affect healing.
  • Corticosteroid creams: may reduce enzymatic activity and delay debridement.
  • Chemotherapeutic agents: may impair wound healing and increase sensitivity.

Frequently Asked Questions

Iruxol Mono is a topical collagenase preparation used to enzymatically debride necrotic tissue in chronic or acute skin wounds, such as venous leg ulcers, diabetic foot ulcers, and pressure injuries, thereby preparing the wound bed for healing.

The enzyme selectively cleaves collagen and other extracellular matrix proteins in dead or damaged tissue. By breaking down the structural framework of necrotic tissue, it facilitates its removal and promotes formation of a clean wound surface that can support new tissue growth.

The specific amount and frequency of Iruxol Mono are determined by the prescribing clinician based on wound size, depth, and patient factors. Dosing instructions are individualized and should follow the healthcare professional’s guidance.

Safety data for Iruxol Mono in pregnancy or lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

Enquiries can be submitted via the product page on gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Iruxol Mono provides enzymatic debridement, which is selective for necrotic collagenous tissue and generally causes less mechanical trauma than surgical or sharp debridement. Compared with other topical enzymes, it offers a well‑characterized collagenase profile and is formulated for easy topical application.

Store Iruxol Mono at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperatures to maintain enzyme activity and product stability.

The product is applied directly to the wound surface using a sterile applicator or gloved finger, covering the necrotic area with a thin, even layer. The treated area is then typically covered with a suitable dressing as directed by the prescriber.

Serious risks include allergic reactions such as hives, swelling, or anaphylaxis, and excessive tissue breakdown leading to severe skin necrosis. Patients should be monitored for signs of systemic hypersensitivity and any unexpected worsening of the wound.

Iruxol Mono should be avoided in individuals with a known hypersensitivity to collagenase, protease enzymes, or any excipients in the formulation, and it is not intended for use on healthy, intact skin or in wounds without necrotic tissue unless directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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