Evaluation of Safety and Efficacy of a Bioengineered Corneal Implant for Treatment of Keratoconus

Keratoconus Clinical Trial

— LinkCor  

Official title:

Evaluation of Safety and Efficacy of Intrastromal Implantation of LinkCor Bioengineered Corneal Implant for Management and Treatment of Keratoconus: a Prospective, Non-randomized, Non-controlled Case Series.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04653922
• Other study ID #: CMG-PRT-001
• Status: Recruiting
• Phase: N/A
• Start date: November 2016
• Est. completion date: July 31, 2024

Study information

• Verified date: April 2022
• Source: LinkoCare Life Sciences AB
• Contact: Mehrdad Rafat, PhD
• Phone: +46734613166
• Email: mrafat[@]linkocare.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, Phase I open-label safety study to evaluate the safety, feasibility and initial efficacy of a bioengineered corneal stromal substitute after implantation into the stroma of adults with advanced keratoconus. The bioengineered substitute and implantation technique may provide a less invasive treatment option for advanced keratoconus than current surgical approaches, that additionally does not rely on the limited availability of human donor corneal tissue.

Description:

This is a Phase I, open-label, non-randomized, non-controlled ongoing clinical case series in two participating centers in Indian and Iranian hospitals, to evaluate the safety and feasibility of minimally-invasive surgery of advanced keratoconus using a bioengineered corneal stromal substitute on a compassionate basis to alleviate blindness and low vision, due to the severely limited availability of human corneal donor tissue at these centers relative to the medical need. Patients fulfilling inclusion criteria are recruited consecutively and implanted intra-stromally with the bioengineered substitute, as a less invasive surgery than full-thickness or anterior lamellar corneal transplantation. In the first phase of the study, a total of 20 patients were recruited and safety and efficacy outcomes were evaluated in those having a minimum of 12 months of postoperative follow-up. In the second phase of the study (currently ongoing), up to 40 patients are being recruited, with one-year postoperative outcomes of all included patients to be evaluated as the final study endpoint. Primary safety and efficacy outcomes will be evaluated.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: July 31, 2024
• Est. primary completion date: December 31, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Advanced keratoconus (according to Amsler-Krumeich classification)

• No corneal scar

• Male or female aged = 18 years, no upper age limit

• Subjects indicated for a first corneal stromal transplantation (treatment naïve)

• Corneal thickness (including epithelium) at least 300µm centrally, as measured by OCT.

• Patients who gave their written signed and dated informed consent for participation

Exclusion Criteria:

• Prior corneal surgery (e.g., refractive surgery, cataract, collagen cross-linking, endothelial keratoplasty, etc.)

• Dry eye / tear film pathology

• Active ocular infection

• Glaucoma / ocular hypertension

• Active corneal ulceration

• Acute or chronic disease or illness that would increase the operation risk or confound the outcomes of the study (immune- compromised, connective tissue disease, clinically significant atopic disease, etc.)

• Any other medical condition that in the judgment of the clinical investigator or corneal surgeon is not compatible with the study procedures

• General history judged by the investigator to be incompatible with the study (e.g., life-threatening patient condition, other condition where postoperative follow-up may be difficult).

• known diabetes or other neuro-degenerative disorder (as corneal nerves can be affected leading to impaired wound healing)

• Inability of patient to understand the study procedures and thus inability to give informed consent.

• Participation in another clinical study within the last 3 months

• Already included once in this study (can only be included for one treated eye).

Related Conditions & MeSH terms

• Keratoconus

Intervention

Device:
• LinkCor Bioengineered Corneal Implant
Intrastromal implantation of a bioengineered corneal equivalent device

Locations

Country	Name	City	State
India	All India Institute of Medical Sciences, Dr. R. P. Centre for Ophthalmic Sciences, AIIMS,	New Delhi
Iran, Islamic Republic of	Farabi Eye Hospital, Tehran University of Medical Sciences	Tehran

Sponsors (1)

Lead Sponsor	Collaborator
LinkoCare Life Sciences AB

Countries where clinical trial is conducted

India,  Iran, Islamic Republic of, 

References & Publications (1)

Rafat M, Jabbarvand M, Sharma N, Xeroudaki M, Tabe S, Omrani R, Thangavelu M, Mukwaya A, Fagerholm P, Lennikov A, Askarizadeh F, Lagali N. Bioengineered corneal tissue for minimally invasive vision restoration in advanced keratoconus in two clinical cohor — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety outcome measure	The primary safety endpoint is defined such that a rejection leading to implant removal should occur in no more than 10% of implanted eyes. The implant rejection is defined as a clinical situation when the implanted eye has decreased central corneal clarity and decreased implant clarity, corneal vascularization inside of laser created pocket and inflammation.	6 months
Primary	Corneal curvature measured by keratometry (efficacy measure)	The maximum and minimum corneal curvature (steepness) of each eye will be measured by a keratometer and reported in diopter (D) unit and represented as "K-value". The efficacy outcome is that more than 60% of the eyes should have a decrease in K-value at 6 months postoperatively.	6 months
Primary	Central corneal thickness measured by topography techniques (efficacy measure)	Central corneal thickness (CCT) will be measured in microns and reported using a two-dimensional thickness map made by optical coherence tomography (OCT) and/or Pentacam topography. The efficacy outcome is that more than 60% of the eyes should have an increase in CCT at 6 months postoperatively.	6 months
Primary	Visual acuity (efficacy measure)	Vision improvement equivalent of minimum one line in Snellen chart in uncorrected distance visual acuity (UDVA) or corrected distance visual acuity (CDVA).	6 months