Allogeneic ABCB5-positive Limbal Stem Cells for Treatment of LSCD

RHEACELL

Status and phase: Active, not recruiting; Phase 2; Phase 1

Conditions: Limbal Stem Cell Deficiency

Treatments: Biological: LSC2

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT03549299

LSC2-II-01

Details and patient eligibility

About

The aim of this clinical trial is to investigate the efficacy (by monitoring neovascularization and epithelial defects) of up to four doses of the investigational medicinal product (IMP) LSC2 topically administered on the target eye of patients with LSCD. Further, safety of the IMP during and after application will be investigated (by monitoring adverse events [AEs]).

Full description

This is an interventional, open-label, phase I/IIa clinical trial to investigate the efficacy and safety of up to four doses of the IMP topically administered on the target eye of patients with LSCD. Patients will be treated in up to four ascending dose groups.

The allogeneic investigational product LSC2 contains ABCB5-positive limbal stem cells (from corneal rims of cadaveric donors, expanded ex vivo, isolated and stored in a donor cell bank).

The IMP will be applied on the target eye. Prior to application, the conjunctival pannus will be removed under general or local anesthesia.

Patients will be followed up for efficacy for 1 year. Efficacy of the IMP will be monitored by assessing neovascularization and epithelial defects.

To assess long-term safety of LSC2 one follow-up visit at Month 24 post IMP application is included.

Enrollment: 16 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female patients aged 18 to 85 years
2. Patients with secondary bilateral or unilateral LSCD (injury that caused LSCD at least 6 months prior to inclusion)
3. Neovascularization: Vessel penetration of at least 2 quadrants, with central cornea involved
4. Patients understand the nature of the procedure and are providing written informed consent prior to any clinical trial procedure
5. Women of childbearing potential must have a negative blood pregnancy test at Visit 1
6. Women of childbearing potential must be willing to use highly effective contraceptive methods during the course of the clinical trial

Exclusion criteria

1. Compromised eyelid mobility and/or symblepharon; patient can be re-screened after appropriate treatment

2. Presence of eyelid malposition; patient can be re-screened after appropriate treatment

3. Active local ocular or systemic infection and/or inflammation. Patient can be re-screened after infection and/or inflammation is resolved.

4. Tumor diseases or history of tumor disease

5. Active ocular neoplastic disease (exclusion will be based on investigator's assessment)

6. Corneal erosion or ulcer is bigger than 4 mm2; corresponding to less than 95% of continuous corneal epithelium. Patient can be re-screened after erosion or ulcer is resolved (≤ 4 mm2).

7. Positive for human immunodeficiency virus (HIV) 1 and/or 2 (diagnosed by serologic testing)

8. Clinically significant or unstable concurrent disease or other clinical contraindications to stem cell transplantation

9. History of glaucoma

10. Contraindications to trial related procedures/substances including

    1. The surgical procedure (e.g. removing of the conjunctival pannus)
    2. Contact lens complications due to contact lens use in the proposed trial (based on the Efron Grading scale for standard clinical reference for contact lens complications)
    3. Tear secretion deficiency determined by Schirmer's test
    4. Allergy, sensitivity or intolerance to components/excipients of the IMP/ per protocol pre-planned concomitant medications
    5. Conjunctival scarring with fornix shortening
    6. General anesthesia (in case general anesthesia is required) or local anesthesia
    7. Immunosuppression (being mandatory concomitant therapy)

11. Intraocular pressure (IOP) of ≥30 mm Hg

12. History or clinical signs of stroke or transient ischemic attacks

13. Active or suspected ocular or periocular infections

14. Active or suspected intraocular inflammation

15. Further clinical contraindications to IMP application (exclusion will be based upon investigator's judgment)

16. Current or previous (within 30 days of enrollment) treatment with another IMP, or participation and/or under follow-up in another clinical trial

17. Previous participation in this clinical trial (except screening failure due to inclusion criterion 2 and/or exclusion criterion 1 and/or 2 and/or 3 and/or 6)

18. Known abuse of alcohol, drugs, or medicinal products

19. Patients unwilling or unable to comply with the requirements of the protocol

20. Lactating women

21. Evidence of any other medical conditions (such as psychiatric illness, physical examination, or laboratory findings) that may interfere with the planned treatment, affect the patient's compliance, or place the patient at high risk of complications related to the treatment

22. Employees of the sponsor, or employees or relatives of the investigator

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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16 participants in 4 patient groups

LSC2; 7.5 x 10^4 cells

Experimental group

Description:

Single dose of LSC2, 7.5 x 10\^4 cells per patient

Treatment:

Biological: LSC2

LSC2; 3.0 x 10^5 cells

Experimental group

Description:

Single dose of LSC2, 3.0 x 10\^5 cells per patient

Treatment:

Biological: LSC2

LSC2; 8.0 x 10^5 cells

Experimental group

Description:

Single dose of LSC2, 8.0 x 10\^5 cells per patient

Treatment:

Biological: LSC2

LSC2; 1.2 x 10^6 cells

Experimental group

Description:

Single dose of LSC2, 1.2 x 10\^6 cells per patient

Treatment:

Biological: LSC2