Safety and Tolerability of hRPC in Retinitis Pigmentosa

NCT ID: NCT02464436

Last Updated: 2023-07-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 29 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-12-31
• Study Completion Date: 2023-12-31

Brief Summary

hRPC is a cell therapy for retinitis pigmentosa. This is a first-in-human, dose escalation study in which participants with retinitis pigmentosa will receive a single subretinal injection of hRPC cells in one eye to evaluate safety and tolerability.

Participants will be followed for two years to evaluate the safety and tolerability of hRPC Additional testing will seek to establish any preliminary efficacy from hRPC.

Detailed Description

This is a first-in-human open label phase I/II dose-escalation study in which participants with retinitis pigmentosa will receive a single uni-ocular subretinal implantation of one of three doses of hRPC.

Treated eyes will be carefully monitored for any ocular or systemic adverse events for 2 years.

Testing will comprise a series of detailed ophthalmic examinations and imaging together with blood testing and systemic evaluations, as necessary.

Ophthalmic testing will also be evaluated for any preliminary efficacy signal.

Conditions

Retinitis Pigmentosa

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

human retinal progenitor cells (hRPC)

Single subretinal administration of human retinal progenitor cells (hRPC)

Group Type: EXPERIMENTAL

hRPC

Intervention Type: DRUG

Participants will undergo vitrectomy surgery and subretinal implantation of hRPC in the study eye.

Interventions

hRPC

Participants will undergo vitrectomy surgery and subretinal implantation of hRPC in the study eye.

Intervention Type: DRUG

Other Intervention Names

human retinal progenitor cells

Eligibility Criteria

Inclusion Criteria

1. Have ability to give written informed consent as evidenced by signature on the subject consent form.

2. Be adult male or female over 18 years of age.

3. Have clinical diagnosis of RP, based upon one or more of the following: clinical features, medical imaging, electrophysiological measures and genetic testing, if available. Genetic confirmation is not obligatory.

4. Have Best Corrected ETDRS visual acuity of 35 letters or less (approximately 20/200 or worse) in the study eye for cohorts 1-5; have Best Corrected ETDRS visual acuity of 63 letters (approximately 20/63) to 36letters (approximately 20/200) in the study eye for cohorts 6-8, and Best Corrected ETDRS visual acuity of 8 letters (approximately 20/800) to 68 letters (approximately 20/50) for cohorts 9 and on.

5. Be able to complete the entire microperimetry test, and demonstrate adequate fixation and consistency between baseline readings such that the accuracy of both baseline and follow on testing should enable the detection of clinically significant changes in retinal sensitivity.

6. Be medically able to undergo vitrectomy and subretinal injection.

7. Have good general health as defined by:

• Normal serum chemistry and hematology. Out of normal range laboratory findings deemed not clinically significant are acceptable.
• No history of malignancy, except non-melanoma skin cancer; pre-malignant conditions and cancer in situ.
• Negative serology for human immunodeficiency virus (HIV), hepatitis B (HBV), hepatitis C (HCV).
• Medically fit enough to undertake surgery which may require general anesthesia as well as medically fit to undergo a short perioperative course of systemic corticosteroid therapy
• Free of any other systemic condition that in the opinion of the Investigator may have an impact on the safety of the subject, conduct of study procedures, or integrity of study data (e.g. severe cardiovascular or respiratory disease; poorly controlled diabetes; significant psychiatric impairment).

8. Females of childbearing potential must have a confirmed negative pregnancy test at Visits 1 and 3; and be willing to use highly effective method of contraception (e.g. oral contraceptive and condom, intra-uterine device (IUD) and condom, diaphragm with spermicide and condom) for the duration of this study.

9. Males must be willing to use a reliable method of contraception (e.g. barrier and spermicide) for the duration of this study; unless have been surgically sterilized with confirmed azoospermia.

10. Be willing and able to attend all scheduled clinical assessments, ability to communicate well with the Investigator and to comply with the expectations of the study.

Exclusion Criteria

1. Exhibits a difference in ETDRS BCVA of 15 letters of more in either eye between any of the baseline visits.

2. Exhibits a difference in ETDRS BCVA of 20 or more letters between eyes at the time of any of the screening or baseline visits attributed to asymmetry in the progression of RP.

3. Presence of ocular disease or ocular media opacity in the study eye, which in the opinion of the Investigator, will preclude an accurate evaluation at any time during the study.

4. History of any retinal and/or macular disease other than RP (e.g. retinal detachment) that in the opinion of the Investigator may have an impact on the safety of the subject, conduct of study procedures, or integrity of study data.Specifically, subjects in whom significant pre-existing vitreoretinal pathology might influence visual acuity outcomes should be excluded

5. Active ocular infection or inflammation, or any history of intraocular inflammation, that would expose subject to risk during or following surgery.

6. Prior vitrectomy in the study eye.

7. A history of amblyopia in the study eye.

8. High myopia (>6 diopters) in the study eye.

9. Cataract surgery in the study eye or ocular surgery in either eye (which in the opinion of the investigator may have an impact on patient safety or the integrity of data from the study eye) during the study or within 3 months prior to treatment.

10. Participation in any clinical study involving an investigational drug or device within 6 months prior to treatment or 5 half-lives of the drug (whichever is longer) prior to initiation of treatment

11. Prior stem cell administration or injections to any part of the body (subjects who have received autologous bone marrow stem cell transplant will be eligible).

12. Use of systemic immunosuppressive agents (e.g. corticosteroid) in the 6 months prior to treatment or 5 half-lives of the drug (whichever is longer) prior to initiation of treatment (Note: inhaled, intranasal, and/or topical dermatologic steroids are allowed)

13. (For females) Be breastfeeding or planning a pregnancy.

m) Known hypersensitivity to any of ingredients of the excipient.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

ReNeuron Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jason Comander, MD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts Eye and Ear Infirmary (MEEI)

Vince Holmes

Role: STUDY_DIRECTOR

ReNeuron Limited

Locations

Retinal Research Institute

Phoenix, Arizona, United States

Massachusetts Eye and Ear Infirmary

Boston, Massachusetts, United States

Oregon Health and Science University

Portland, Oregon, United States

Institut de la Màcula

Barcelona, , Spain

Oxford Eye Hospital

Oxford, , United Kingdom

Countries

United States; Spain; United Kingdom

Other Identifiers

RN03-CP-0001

Identifier Type: -

Identifier Source: org_study_id