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

Iruxol N

Active Ingredient:
Collagenase Clostridium Histolyticum, Protease
Origin:
EU

Iruxol N (Collagenase Clostridium Histolyticum, Protease)

Collagenase Clostridium Histolyticum, the active ingredient in Iruxol N, is an enzyme (collagenase) presented as a cutaneous formulation for topical use. It is employed to debride necrotic tissue in chronic wounds, pressure ulcers and diabetic foot ulcers.

GNH India supplies Iruxol N 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 N, an enzymatic debridement agent, is used in wound care to remove necrotic tissue and improve healing.

  • Pressure ulcers: facilitates removal of necrotic tissue and promotes granulation tissue formation.
  • Diabetic foot ulcers: aids debridement of chronic lesions, supporting faster wound closure.
  • Chronic non‑healing wounds: enzymatically clears extracellular matrix debris to improve the wound bed.

How It Works

  • Collagenase Clostridium Histolyticum hydrolyzes native collagen and other extracellular matrix proteins at the wound surface. By breaking down fibrillar collagen, the enzyme loosens necrotic tissue, allowing mechanical removal and exposing viable tissue, which accelerates granulation and re‑epithelialisation in chronic wounds.

Side Effects

Local and systemic reactions may occur with Iruxol N; reported events are categorized by frequency.

Common Side Effects

  • Local pain or burning sensation at the application site.
  • Redness or erythema around the treated area.
  • Swelling or edema of the surrounding skin.
  • Mild itching or pruritus.
  • Slight bleeding or oozing from the debrided tissue.
  • Increased wound drainage.

Serious or Rare Side Effects

  • Allergic reaction including anaphylaxis.
  • Severe infection of the treated wound.
  • Unintended tissue necrosis extending beyond target area.
  • Systemic hypersensitivity responses.
  • Significant hemorrhage.
  • Deep ulceration or perforation.

Precautions & Warnings

Iruxol N should be used under professional supervision with attention to wound characteristics and patient safety.

  • Assess wound type: ensure the wound contains necrotic tissue suitable for enzymatic debridement.
  • Avoid application on healthy or granulating tissue.
  • Monitor for signs of infection or excessive pain during treatment.
  • Do not combine with other topical proteolytic enzymes unless directed by a clinician.
  • Use only as prescribed by a qualified healthcare provider.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Iruxol N may interact with other topical agents or systemic medications that affect coagulation or wound healing.

Major Interactions (Avoid)

  • Concurrent use of other proteolytic enzymes, which can amplify tissue breakdown.
  • Systemic anticoagulants (e.g., warfarin, heparin) increasing bleeding risk at the application site.
  • Topical antibiotics containing oxidizing agents that may inactivate the collagenase.

Moderate Interactions (Monitor Closely)

  • Moisturizers or dressings containing zinc oxide or high protein content that could bind the enzyme.
  • Radiation therapy applied to the same wound area, potentially altering enzyme activity.
  • Use with corticosteroid creams, which may reduce local inflammatory response and affect efficacy.
  • Application over areas treated with chemical cautery or laser therapy.

Frequently Asked Questions

Iruxol N is a topical enzymatic preparation used to debride necrotic tissue in chronic wounds such as pressure ulcers, diabetic foot ulcers and other non‑healing wounds. By removing dead tissue, it helps create a cleaner wound bed that can support faster healing under professional care.

The collagenase component selectively breaks down collagen fibers and other extracellular matrix proteins in necrotic tissue. This enzymatic degradation loosens and dissolves dead tissue, allowing it to be removed more easily and exposing healthy tissue that can progress through the normal stages of wound repair.

The dosage and frequency of Iruxol N are determined by the prescribing clinician based on wound size, depth and patient condition. The product is applied topically to the affected area as directed, and the treatment plan is individualized for each patient.

Safety data for Collagenase Clostridium Histolyticum in pregnancy or lactation are limited. Use of Iruxol N during pregnancy or while breastfeeding should only be considered if the potential benefit justifies any potential risk to the fetus or infant, and it must be decided by the treating physician.

To request Iruxol N, submit an enquiry on the product page at gnhindia.com indicating 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 (including cold‑chain if required) and necessary import documentation.

Iruxol N provides enzymatic debridement, which is less invasive than surgical or mechanical methods and can be applied to delicate or hard‑to‑reach areas. Compared with chemical agents, it offers more selective collagen breakdown, reducing damage to healthy tissue while still efficiently removing necrotic material.

Iruxol N should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight and extreme temperatures to maintain enzyme stability. Follow any specific handling instructions on the label before application.

Iruxol N is applied directly to the wound surface as a topical preparation. The clinician cleans the wound, applies the prescribed amount of the enzyme preparation, and may cover it with an appropriate dressing. The frequency of application is determined by the treating professional.

Serious risks include allergic reactions such as anaphylaxis, severe infection of the treated wound, unintended tissue necrosis beyond the target area, and significant bleeding. Patients should be monitored closely for any signs of these events, and treatment should be discontinued if they occur.

Iruxol N should not be used on healthy, non‑necrotic tissue, in patients with known hypersensitivity to collagenase or any component of the formulation, or in wounds where enzymatic debridement is contraindicated (e.g., active uncontrolled infection without appropriate antimicrobial therapy).

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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