Skip to content

What is the difference between ikervis and verkazia?

3 min read

While Ikervis and Verkazia both contain the same concentration of the active immunosuppressant ciclosporin, the key distinction lies in their approved indications, target patient populations, and dosing schedules. Both are ophthalmic emulsions, but the question, “What is the difference between ikervis and verkazia?” comes down to what specific inflammatory eye disease they are licensed to treat.

Quick Summary

Ikervis is for treating severe keratitis from dry eye disease in adults, while Verkazia is for vernal keratoconjunctivitis (VKC) in patients aged 4 and up. Despite sharing the same active ingredient and concentration, their specific indications and dosing frequencies differ, necessitating brand-name prescribing.

Key Points

  • Active Ingredient and Concentration: Both Ikervis and Verkazia contain the same concentration (0.1%) of the active immunosuppressant ciclosporin.

  • Indication: Ikervis is for severe keratitis in adult dry eye patients, while Verkazia is for vernal keratoconjunctivitis (VKC).

  • Target Population: Ikervis is for adults only, whereas Verkazia can be used in children as young as 4, as well as adults.

  • Formulation: Both use an identical cationic emulsion formulation to enhance drug absorption.

  • Prescribing: Brand-name prescribing is essential to ensure the correct medication is used for the patient's specific age and condition.

In This Article

Both Ikervis and Verkazia are immunosuppressant eye drops containing ciclosporin (also known as cyclosporine) at a concentration of 1 mg/mL (0.1%). They also share the same innovative cationic emulsion formulation, which is designed to enhance the bioavailability of ciclosporin on the eye's surface. However, their primary differences stem from their separate regulatory approvals for specific inflammatory conditions, which dictate their respective use, dosing, and target demographics.

Ikervis: For Adult Dry Eye Disease

Ikervis is approved for the treatment of severe keratitis, an inflammation of the cornea, in adult patients with dry eye disease (DED). It is used when a patient's condition has not adequately responded to treatment with artificial tears. The clinical rationale is to address the underlying inflammatory component of severe DED.

Key features of Ikervis's use include:

  • Target Population: Exclusively adults (aged 18 years and over).
  • Condition: Severe keratitis associated with dry eye disease.

Verkazia: For Vernal Keratoconjunctivitis (VKC)

Verkazia is indicated for a different and rarer inflammatory eye condition called vernal keratoconjunctivitis (VKC), which is a chronic allergic inflammation. Unlike DED, VKC often affects children and adolescents, and Verkazia is approved for patients as young as four years of age.

Key features of Verkazia's use include:

  • Target Population: Children aged 4 and up, adolescents, and adults with VKC.
  • Condition: Severe vernal keratoconjunctivitis.
  • Orphan Drug Status: Verkazia was granted orphan drug status for VKC due to the rarity of the condition.

Comparison Table: Ikervis vs. Verkazia

Feature Ikervis Verkazia
Active Ingredient Ciclosporin (Cyclosporine) Ciclosporin (Cyclosporine)
Concentration 1 mg/mL (0.1%) 1 mg/mL (0.1%)
Formulation Cationic Ophthalmic Emulsion Cationic Ophthalmic Emulsion
Approved Indication Severe keratitis in adult dry eye disease not responsive to tear substitutes. Severe vernal keratoconjunctivitis (VKC).
Target Population Adults (≥ 18 years). Children (≥ 4 years), adolescents, and adults.
Regulatory Status Standard approval for DED. Orphan drug status for VKC.

Clinical Considerations and Prescribing

Because Ikervis and Verkazia share the same drug and concentration but are prescribed for different patient populations and conditions, it is crucial for healthcare professionals to prescribe the medication by its specific brand name. This practice helps avoid confusion and ensures that the patient receives the correct treatment intended for their condition.

Patients should also be aware of the storage requirements for both medications. They are provided in sterile, single-dose vials and must be kept in their foil pouches to protect from light and evaporation. Any unused portion of a vial must be discarded immediately after use, as they do not contain preservatives.

Potential Side Effects

Both eye drops can cause side effects, many of which are similar due to the shared active ingredient. Common side effects reported include eye pain or irritation upon instillation, ocular hyperaemia (redness), and blurred vision. These side effects are often temporary and resolve as the eye adjusts to the medication. It is important to remove contact lenses before using either medication and wait at least 15 minutes before reinserting them.

Conclusion

The difference between Ikervis and Verkazia, despite their identical core drug and concentration, is primarily defined by their distinct regulatory approvals and indications. Ikervis is specifically for managing severe keratitis in adults with dry eye disease, while Verkazia targets vernal keratoconjunctivitis in children and adults. This highlights the importance of matching the specific medication brand to the correct diagnosis and patient age group, ensuring effective and appropriate treatment for these inflammatory ocular conditions. You can find more detailed information on their respective uses by visiting the European Medicines Agency's website for Ikervis and Verkazia product information.

Frequently Asked Questions

No, Ikervis is only approved for treating severe keratitis associated with dry eye disease in adults. Verkazia is the ciclosporin eye drop specifically approved for treating VKC.

No, Verkazia is not approved for treating DED. Its specific indication is for vernal keratoconjunctivitis. Ikervis is the ciclosporin product designed for severe keratitis in adults with DED.

Yes, both Ikervis and Verkazia contain the same active ingredient, ciclosporin, at the same concentration of 1 mg/mL or 0.1%.

The different dosing schedules are a result of their clinical trials and regulatory approval process for two distinct conditions. The optimal frequency was determined based on the specific inflammatory eye condition being treated (DED versus VKC).

Both medications are considered safe and well-tolerated for their respective approved uses. Any differences in side effect profiles are typically related to the underlying disease being treated, not the drug itself.

It is important to prescribe by brand name to prevent potential confusion. While they share the same active ingredient and concentration, their specific approved indications and dosage schedules are different, which is crucial for appropriate patient care.

Both Ikervis and Verkazia use an identical cationic emulsion formulation. This allows for better adherence of the medication to the negatively charged ocular surface, improving the delivery and bioavailability of the ciclosporin.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.