NCT02464436进行中（未招募）1 期
First-in-human Phase I/IIa, Open-Label, Prospective Study of the Safety and Tolerability of Subretinally Transplanted Human Retinal Progenitor Cells (hRPC) in Patients With Retinitis Pigmentosa (RP)
适应症
干预措施
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 29
- 试验地点
- 5
- 主要终点
- Safety over the six months after treatment as assessed by the incidence of treatment emergent adverse events (TEAEs) and changes from baseline in other safety parameters.
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Have ability to give written informed consent as evidenced by signature on the subject consent form.
- •Be adult male or female over 18 years of age.
- •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.
- •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.
- •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.
- •Be medically able to undergo vitrectomy and subretinal injection.
- •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).
- •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.
- •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.
- •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.
排除标准
- •Exhibits a difference in ETDRS BCVA of 15 letters of more in either eye between any of the baseline visits.
- •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.
- •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.
- •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
- •Active ocular infection or inflammation, or any history of intraocular inflammation, that would expose subject to risk during or following surgery.
- •Prior vitrectomy in the study eye.
- •A history of amblyopia in the study eye.
- •High myopia (>6 diopters) in the study eye.
- •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.
- •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
- •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).
- •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)
- •(For females) Be breastfeeding or planning a pregnancy.
- •m) Known hypersensitivity to any of ingredients of the excipient.
研究组 & 干预措施
human retinal progenitor cells (hRPC)
Experimental
Single subretinal administration of human retinal progenitor cells (hRPC)
干预措施: hRPC (Drug)
结局指标
主要结局
Safety over the six months after treatment as assessed by the incidence of treatment emergent adverse events (TEAEs) and changes from baseline in other safety parameters.
时间窗: 6 months
Safety measures will be assessed by review of important events, including but not limited to inflammation, complications of the surgical procedure and worsening of vision.
次要结局
- Safety (Visual function measure: change in visual field: Goldmann visual field, microperimetry and FST)(24 months)
- Safety (Anatomical endpoint relating to retinal function in implant location - Color Fundus Photography)(24 months)
- Safety (Anatomical endpoint relating to retinal function in implant location - Fundus autofluorescence)(24 months)
- Safety (Anatomical endpoint relating to retinal function in implant location - Spectral domain-OCT)(24 months)
- Safety (Change in retinal sensitivity in the area overlying the implanted hRPC as compared with untreated retina)(24 months)
- Safety (Visual function measure: change in visual acuity)(24 months)
研究者
研究点 (5)
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