GNH USA

Europe — EMA

Holoclar

Holoclar is an autologous cell‑therapy cell sheet for limbal stem‑cell deficiency due to ocular burns, restoring corneal epithelium in the EU.

Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells

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What is Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells?

Holoclar is an autologous cell‑therapy product whose active ingredient is ex vivo expanded autologous human corneal epithelial cells containing stem cells. It is supplied as a sterile cell sheet for implantation onto the ocular surface. The preparation contains no added drug substance, and it is prescribed as a prescription‑only (Rx) therapy for patients with limbal stem‑cell deficiency in the European Union and is used under specialist ophthalmic care.

What is Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells used for?

Holoclar is indicated for the reconstruction of the ocular surface in patients with limbal stem‑cell deficiency caused by ocular burns.

- Restoration of corneal epithelium in unilateral limbal stem‑cell deficiency. - Treatment of persistent epithelial defects after chemical injury. - Adjunct therapy following surgical removal of scar tissue in the limbal region. - Use in cases where autologous limbal tissue can be harvested and expanded ex vivo. - Consideration for patients with partial limbal loss where conventional grafts are unsuitable.

What are the side effects of Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells?

Adverse reactions reported after Holoclar implantation involve ocular and systemic events, most of which are mild and transient.

Common: - Conjunctival hyperemia - Mild ocular irritation or foreign‑body sensation - Transient increase in intra‑ocular pressure - Mild corneal edema

Serious: - Graft failure or loss of epithelial integrity - Infectious keratitis - Neovascularization of the cornea

What precautions apply to Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells?

Clinicians should observe several precautions before and after Holoclar implantation to minimize complications.

- Verify that sufficient autologous limbal tissue can be harvested without compromising the donor eye. - Perform a thorough ocular surface assessment to rule out active infection. - Ensure proper storage and handling of the cell sheet according to manufacturer guidelines. - Monitor intra‑ocular pressure and corneal thickness during the postoperative period. - Advise patients to avoid eye rubbing and exposure to contaminants. - Schedule regular follow‑up examinations to assess graft integration. - Use systemic immunosuppression only if indicated, as the product is autologous.

What does Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells interact with?

Holoclar may interact with other ocular medications or systemic agents that affect wound healing or immune response.

Avoid: - Topical corticosteroids at high potency immediately after implantation without physician supervision. - Systemic immunosuppressants unless specifically prescribed for graft rejection. - Antifungal or antiviral eye drops that contain preservatives known to be toxic to corneal epithelium.

Use with caution: - Preservative‑free lubricants and antibiotics, monitoring for delayed epithelial healing. - Anti‑VEGF agents if neovascularization develops, balancing risk of impaired graft survival. - Contact lens wear, ensuring proper fitting and hygiene to prevent mechanical trauma.

Frequently asked questions

What type of product is Holoclar?+
Holoclar is an autologous cell‑therapy supplied as a sterile cell sheet that contains ex vivo expanded human corneal epithelial cells with stem cells for implantation onto the eye.
For which condition is Holoclar approved in the European Union?+
Holoclar is approved for the treatment of limbal stem‑cell deficiency caused by ocular burns.
How is Holoclar administered?+
The product is implanted surgically onto the damaged limbal region of the cornea as a cell sheet.
Can Holoclar be used in both eyes simultaneously?+
Holoclar is typically used for unilateral disease; each eye requires its own autologous cell sheet derived from the patient’s own limbal tissue.
What is the source of the cells in Holoclar?+
The cells are harvested from the patient’s own limbal tissue, expanded ex vivo in a laboratory, and then formed into a sheet for re‑implantation.
Is Holoclar a prescription‑only medication?+
Yes, Holoclar is classified as a prescription‑only (Rx) therapy and must be prescribed by a qualified ophthalmologist.
What are common side effects after Holoclar implantation?+
Common adverse events include conjunctival hyperemia, mild ocular irritation, transient increase in intra‑ocular pressure, and mild corneal edema.
What serious complications can occur with Holoclar?+
Serious complications may include graft failure, infectious keratitis, and corneal neovascularization.
Are there any special storage requirements for Holoclar?+
Yes, the cell sheet must be stored at controlled temperatures and handled according to the manufacturer’s guidelines to maintain cell viability.
Can Holoclar be combined with other eye drops after surgery?+
It can be combined with preservative‑free lubricants and antibiotics, but the use of high‑potency corticosteroids or preservative‑containing drops should be discussed with the surgeon.
What follow‑up care is recommended after Holoclar implantation?+
Patients should have regular ophthalmic examinations to monitor graft integration, intra‑ocular pressure, and corneal health, typically at intervals defined by the treating specialist.
Is Holoclar suitable for patients with bilateral limbal deficiency?+
Holoclar is primarily indicated for unilateral disease; bilateral cases may require alternative strategies such as allogeneic grafts or other cell‑based therapies.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Ex Vivo Expanded Autologous Human Corneal Epithelial Cells Containing Stem Cells
Route
Implantation
Manufacturer
Holostem S.R.L.
Origin
EU

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