About Corneal Blindness
Diseases affecting the cornea are a major cause of blindness worldwide. According to the World Health Organization, approximately 2 million new cases of corneal blindness are reported each year. Over 30 million people in the world are legally blind in one or both eyes from corneal injury and disease, while many more suffer from degraded visual acuity. A recent study published in JAMA Ophthalmology* assessed the shortage of corneas at one available cornea for 70 needed.
Several attempts to develop an artificial cornea have failed in creating robust, scalable and reliable solutions. As such, there exists an unmet need for an efficient, long-lasting and affordable solution to corneal pathology, injury and blindness, which would alleviate this suffering and disability and enable patients to fully exploit their vision potential.
*Gain P, Jullienne R, He Z, et al. Global Survey of Corneal Transplantation and Eye Banking. JAMA Ophthalmol. 2016;134(2):167–173. doi:10.1001/jamaophthalmol.2015.4776
Global Demand
World map showing the supply and demand of corneal transplantation in 148 countries.
"Our survey globally quantified the considerable shortage of corneal graft tissue, with only one cornea available for 70 needed. Efforts to encourage cornea donation must continue in all countries, but it is also essential to develop alternative and/or complementary solutions, such as corneal bio-engineering."*
*Gain P, Jullienne R, He Z, et al. Global Survey of Corneal Transplantation and Eye Banking. JAMA Ophthalmol. 2016;134(2):167–173. doi:10.1001/jamaophthalmol.2015.4776
CorNeat KPro Advantages
CorNeat KPro is superior to keratoplasty and current keratoprosthetics in the following aspects
Optical Performance
Replicating optimal corneal optics
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Wide field of view
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Simplifying the surgical procedure via direct visualization while
enabling future procedures in a similar fashion
Healing and Retention
Device integrates to the eye wall using nano-fabric that imitates the native ECM
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Fast to heal
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Progressive integration
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Straight forward post-operation recovery
Scalability
Relatively simple, 45-minute operation
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Affordable price
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No time constraints placed on scheduling of the implantation
Safety
No need for tissue
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Cannot carry any infectious agent including COVID-19
CorNeat KPro
The CorNeat KPro is a patented synthetic cornea, which provides a long-lasting medical solution for corneal blindness, pathology and injury. The CorNeat KPro allows corneally blind patients to fully rehabilitate normal vision, immediately following a relatively straightforward implantation procedure. It is a unique and innovative device that utilizes a skirt made out of the CorNeat EverMatrix™ to integrate artificial optics within resident ocular tissue, relieving the need for donor tissue.
Current biological solutions and previous KPros are either sutured to, or attempt integration with, the native corneal tissue, a tissue that lacks blood vessels and heals very poorly. In contrast, the CorNeat KPro reliably integrates underneath the conjunctiva, a vascularized site rich with fibroblasts, which heals quickly and vigorously.
The CorNeat KPro is implanted using a novel and straightforward surgical procedure providing an efficient, therapeutic, and affordable remedy for millions of people with cornea-related visual impairments and is far superior to any available alternative.
Features, Surgical Kit and Procedure
The CorNeat KPro implantation procedure is relatively straightforward and does not require the delicate suturing process needed for connecting the donor corneal tissue to the patient’s native cornea and optically aligning it. The CorNeat KPro snaps into the patient’s trephined cornea and is then sutured to the eye using three non-degradable sutures.
The surgical tools supplied as part of the implantation kit: the marker and the snapper, yield a systematic and accurate implantation process. This procedure is easy to teach and can be learned within a couple of days. The operation minimizes the time the trephined eye is exposed (open sky) to less than one minute, significantly reducing associated risks.
The CorNeat KPro implant's patented design is the result of an extensive, multidisciplinary research and development process. The device, and its wide aperture PMMA lens, provides unprecedented visual performance and a wide field of view, which is significantly superior to tissue and predicates. This also allows physicians to examine the patient's eye and perform surgical procedures post-implantation. An undercut on the posterior side enables the device to easily snap into a trephined cornea and quickly seal the eye. The CorNeat KPro lens is surrounded by a non-degradable porous integrating skirt, which is implanted subconjunctivally.
Once implanted, the skirt material stimulates cellular proliferation and colonization that progressively leads to full tissue integration. The skirt, which is only 100-150 microns in thickness, also includes a set of holes around its circumference through which the conjunctiva adheres to the sclera. Additional holes on the circumference of the lens, which are filled with the same porous material, assist in anchoring the lens to the sclera by means of bio-stitching, as tissue is expected to grow through this area. This process anchors the device to the sclera, ensuring long-term retention. These features together are designed for long-term and reliable integration.
Three pairs of suturing holes on the rim of the lens increase safety. These holes enable the ophthalmologist to secure the device to the eye within minutes. Suturing the device stabilizes the lens, significantly easing the implantation procedure. This also stabilizes the skirt post-operation, which is key to successful biological integration.
The CorNeat KPro lens is designed to enable post-operative ophthalmic examinations and subsequent anterior and posterior segment surgeries (i.e. cataract and retinal surgeries). This is achieved with four openings or “ports,” located on the rim of the lens, at the limbus. Four corresponding indicators which can be viewed through an ophthalmic microscope, direct the surgeon to these ports' locations. This is required as they are located and placed subconjunctivally.
The CorNeat KPro solution is 100% synthetic and does not require the use of donor tissue, therefore it is widely accessible and safe. The device cannot carry infectious agents or cause excessive inflammation, resulting in improved quality of life and more effective patient care.
Indications
Failed keratoplasty
Corneal indications not suitable for keratoplasty, such as:
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Herpes keratitis
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Corneal degenerations
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ICE syndrome
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Aniridia
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SJS
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OCP
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Alkali burns
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Vascularized cornea
First-In-Human (FIH) Implantation
CorNeat Vision successfully completed the First-in-Human trial of the CorNeat KPro which proved the device’s integration concept, optics, and surgical technique. The study enabled a number of corneally blind patients to regain their sight and independence.
Below at the top left you can see two pictures of the patient's eye. The top picture was taken before the operation and the middle picture was taken immediately following the operation. The dramatic aesthetic impact was already apparent. A couple of weeks later, once the eye healed, the patient's eye looked completely natural.
Below at the bottom left you can see the OCT image, taken immediately following the operation. The corneal remnant sits securely in the undercut and the skirt material is covered with conjunctiva.
At the right you can see the patient's eye with the CorNeat KPro a few months post implantation.
Clinical Trial
A second clinical trial was initiated in 2024 in Paris, with additional sites planned in Israel, Canada, The Netherlands and India. The study will be extended to the US and China in 2025. The second clinical trial implements several improvements in the surgical technique, and the pre/post op treatment. Patient inclusion and exclusion criteria were also refined. Several improvements in the device which are aimed at accelerating tissue integration have been implemented as well.
For more information about clinical trials please visit clinicaltrials.gov.
Regulatory Path
CorNeat Vision is meticulously adhering to the requirements outlined in the FDA Guidance on 510(k) Submissions for Keratoprostheses, as well as incorporating insights gathered from regulatory authorities. This commitment ensures strict compliance with regulatory standards for obtaining marketing approvals in the US, Europe, and China. The company anticipates securing initial marketing approval for the CorNeat KPro late in 2025.
Product Animation
Q&A
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Would a person with severe dry eye be a candidate for the CorNeat KPro implantation?Initially we will treat patients with some tear production. With the accumulation of experience, we will collect the necessary evidence to encourage surgeons to tackle the most challenging and arid ophthalmic patients, suffering from alkali chemical burn, Stevens-Johnson Syndrome or ocular cicatricial pemphigus.
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Would a person with Stevens-Johnson Syndrome be a candidate for the CorNeat KPro implantation?See previous answer.
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Would a person with herpes keratitis be a candidate for the CorNeat KPro implantation?Yes, we believe that herpes keratitis patients stand to gain a valid therapeutic modality, which is currently missing in the battery of clinical ophthalmic solutions.
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Would a person with a scarred cornea be a candidate for the CorNeat KPro implantation?Scarred, opaque and/or vascularized corneas are excellent candidates for the CorNeat KPro.
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Would a person who had laser correction surgery be a candidate for the CorNeat KPro implantation?Yes, laser correction does not interfere with the CorNeat KPro implantation procedure.
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Would a person who had a corneal transplantation (one or more) which was/were rejected be a candidate for the CorNeat KPro implantation?Yes, patients with failed corneal grafts are our ideal candidates for implantation.
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What are the differences between the CorNeat KPro and the Boston KPro?The major differences between the two implants are i) The Boston KPro utilizes donor cornea tissue to attach the synthetic lens to the eye whereas the CorNeat KPro is completely synthetic eliminating the need for harvesting tissue to bridge the gap between the artificial lens and the patients eye. ii) The Boston KPro provides a narrow field of view both for the patient and the physician. This limits the ability of the practitioner to follow up on the eye’s health and intervene in time. Following implantation of the Boston KPro, access to the internal ocular compartments is blocked thus surgical procedures cannot be carried out. The CorNeat KPro is engineered with bays on the optic’s rim to enable anterior chamber access following implantation and will stay accessible throughout the patient’s life. Posterior chamber access is readily available through the device’s integrating element, which should stay accessible throughout life as well. This will also allow the ophthalmologist to perform regular and thorough follow-up and timely interventions as needed. The CorNeat KPro has a wide field of view similar to the native cornea providing the patient with real-life optics and restoring an aesthetic appearance. iii) The Boston KPro is a temporary solution, which needs to be replaced once every few years, when all goes well, or it permanently damages the eye's visual potential through a variety of complications. The CorNeat KPro is engineered to be a permanent solution with robust integration into the eye’s tissues.
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Where will the CorNeat KPro clinical trials take place?The CorNeat KPro clinical trial is taking place in Israel, Canada, France, the Netherlands and India and are planned to start in the USA in 2026.
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When will the CorNeat KPro be available for use?The CorNeat KPro launch is planned for 2027.
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What will the selection criteria be for patients for the CorNeat KPro implantation?Initially, the CorNeat KPro will be approved as a second-line treatment, only patients who lack a therapeutic alternative or have failed a corneal transplantation will be eligible for the procedure. Approval of the CorNeat KPro as a first-line treatment is a priority for CorNeat Vision and will follow the initial approval.
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Would a person with keratoconus be a candidate for the CorNeat KPro implantation?Keratoconus patients are suitable candidates for corneal transplantation with positive long-term results. Therefore, they are not ideal candidates for primary implantation. The CorNeat KPro is a viable solution in cases where a Keratoconus patient fails corneal transplantation for any reason, as a second-line treatment.
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Would a person with a detached retina be a candidate for the CorNeat KPro implantation?Such a patient would not be a good candidate as the CorNeat KPro mandates visual potential. Retinal issues, optic nerve function and other issues affecting visual potential need to be dealt with prior to attempting implantation of the CorNeat KPro.
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Would a person with glaucoma be a candidate for the CorNeat KPro implantation?Glaucoma is not a contraindication for the CorNeat KPro implantation. Glaucoma should be a consideration when planning the surgery as adjunct procedures, changes in drug regimen and visual potential might vary between glaucoma patients undergoing CorNeat KPro implantation. These factors impact eligibility and surgical and post-op planning.
-
Would a person with severe dry eye be a candidate for the CorNeat KPro implantation?Initially we will treat patients with some tear production. With the accumulation of experience, we will collect the necessary evidence to encourage surgeons to tackle the most challenging and arid ophthalmic patients, suffering from alkali chemical burn, Stevens-Johnson Syndrome or ocular cicatricial pemphigus.
-
Would a person with Stevens-Johnson Syndrome be a candidate for the CorNeat KPro implantation?See previous answer.
-
Would a person with herpes keratitis be a candidate for the CorNeat KPro implantation?Yes, we believe that herpes keratitis patients stand to gain a valid therapeutic modality, which is currently missing in the battery of clinical ophthalmic solutions.
-
Would a person with a scarred cornea be a candidate for the CorNeat KPro implantation?Scarred, opaque and/or vascularized corneas are excellent candidates for the CorNeat KPro.
-
Would a person who had laser correction surgery be a candidate for the CorNeat KPro implantation?Yes, laser correction does not interfere with the CorNeat KPro implantation procedure.
-
Would a person who had a corneal transplantation (one or more) which was/were rejected be a candidate for the CorNeat KPro implantation?Yes, patients with failed corneal grafts are our ideal candidates for implantation.
-
What are the differences between the CorNeat KPro and the Boston KPro?The major differences between the two implants are i) The Boston KPro utilizes donor cornea tissue to attach the synthetic lens to the eye whereas the CorNeat KPro is completely synthetic eliminating the need for harvesting tissue to bridge the gap between the artificial lens and the patients eye. ii) The Boston KPro provides a narrow field of view both for the patient and the physician. This limits the ability of the practitioner to follow up on the eye’s health and intervene in time. Following implantation of the Boston KPro, access to the internal ocular compartments is blocked thus surgical procedures cannot be carried out. The CorNeat KPro is engineered with bays on the optic’s rim to enable anterior chamber access following implantation and will stay accessible throughout the patient’s life. Posterior chamber access is readily available through the device’s integrating element, which should stay accessible throughout life as well. This will also allow the ophthalmologist to perform regular and thorough follow-up and timely interventions as needed. The CorNeat KPro has a wide field of view similar to the native cornea providing the patient with real-life optics and restoring an aesthetic appearance. iii) The Boston KPro is a temporary solution, which needs to be replaced once every few years, when all goes well, or it permanently damages the eye's visual potential through a variety of complications. The CorNeat KPro is engineered to be a permanent solution with robust integration into the eye’s tissues.
-
Where will the CorNeat KPro clinical trials take place?The CorNeat KPro clinical trial is taking place in Israel, Canada, France, the Netherlands and India and are planned to start in the USA in 2026.
-
When will the CorNeat KPro be available for use?The CorNeat KPro launch is planned for 2027.
-
What will the selection criteria be for patients for the CorNeat KPro implantation?Initially, the CorNeat KPro will be approved as a second-line treatment, only patients who lack a therapeutic alternative or have failed a corneal transplantation will be eligible for the procedure. Approval of the CorNeat KPro as a first-line treatment is a priority for CorNeat Vision and will follow the initial approval.
-
Would a person with keratoconus be a candidate for the CorNeat KPro implantation?Keratoconus patients are suitable candidates for corneal transplantation with positive long-term results. Therefore, they are not ideal candidates for primary implantation. The CorNeat KPro is a viable solution in cases where a Keratoconus patient fails corneal transplantation for any reason, as a second-line treatment.
-
Would a person with a detached retina be a candidate for the CorNeat KPro implantation?Such a patient would not be a good candidate as the CorNeat KPro mandates visual potential. Retinal issues, optic nerve function and other issues affecting visual potential need to be dealt with prior to attempting implantation of the CorNeat KPro.
-
Would a person with glaucoma be a candidate for the CorNeat KPro implantation?Glaucoma is not a contraindication for the CorNeat KPro implantation. Glaucoma should be a consideration when planning the surgery as adjunct procedures, changes in drug regimen and visual potential might vary between glaucoma patients undergoing CorNeat KPro implantation. These factors impact eligibility and surgical and post-op planning.