- AAV-RPE65 met the primary endpoint of safety and tolerability
- Statistically significant improvement demonstrated in vision-guided mobility and visual function in treated eyes compared to untreated eyes
- Dose selected for pivotal study; Company expects to meet with global regulatory authorities in the second half of 2019
MeiraGTx Holdings plc announced positive data from a Phase 1/2 dose escalation trial of AAV-RPE65, the Company’s investigational gene therapy for the treatment of RPE65-deficiency, a condition that causes blindness. AAV-RPE65 is a second-generation gene therapy candidate developed specifically to treat RPE65-deficiency, and optimized for transduction efficiency, potency and stability. The trial achieved the primary endpoint of safety and tolerability of AAV-RPE65. Additionally, AAV-RPE65 demonstrated statistically significant improvement across several secondary endpoints designed to assess clinical activity.
The Phase 1/2 open-label, multi-center, dose-finding trial evaluated AAV-RPE65 in patients with retinal dystrophy associated with disease-causing variants in the RPE65 gene. The trial was conducted at two centers in the U.S. and UK, and three surgeons undertook the surgery across these sites. The trial enrolled 15 patients, including nine young adults (aged 16-24 years old) across three dose escalation cohorts, and six children (aged 5-12 years old) in a pediatric expansion cohort. Each patient was treated with subretinal delivery of AAV-RPE65 in the eye that was more affected at baseline. The patient’s other eye served as an untreated control.
Significant improvement in vision was demonstrated at six months after AAV-RPE65 treatment, as measured by assessments of vision-guided mobility, retinal sensitivity, visual acuity and contrast sensitivity. Larger improvements from baseline in functional vision were observed between treated and control eyes at lower light levels. These outcomes address the core functional manifestation of RPE65-deficiency, which typically causes vision impairment beginning in early childhood that is most pronounced in low-light conditions, and is consistent with the proposed mechanism of action of AAV-RPE65.
MeiraGTx intends to meet with regulatory authorities in the second half of 2019 to define the development pathway for regulatory approval of AAV-RPE65.
“RPE65-deficiency profoundly impacts quality of life from childhood and leads to increasing disability as patients progress toward complete loss of vision,” said Michel Michaelides, trial investigator, Professor of Ophthalmology, University College London, and Head of Clinical Ophthalmology, MeiraGTx. “This trial demonstrated that AAV-RPE65 has the potential to restore vision in a severely debilitating disease. These highly encouraging early data reflect the promise of gene therapy to change the lives of patients with blinding inherited retinal diseases.”
Full data from the Phase 1/2 trial is expected to be presented in a scientific forum later this year.
Topline Data from Phase 1/2 Trial of AAV-RPE65
Dose escalation in adults began at a potentially therapeutically relevant dose of 1×1011 vg/ml in Cohort 1. Cohorts 2 and 3 were treated with increasing doses of 3×1011 vg/ml and 1×1012 vg/ml, respectively. Dose escalation was successfully completed, with three adults treated sequentially in each cohort.
In Cohorts 1, 3, and the pediatric expansion cohort, subretinal injections targeted the central retina including the fovea. In Cohort 2, subretinal injections were peripheral to the fovea.
Based on the encouraging efficacy and safety observed in adults treated in Cohort 1 (1×1011 vg/ml), this dose was selected for use in a pediatric expansion cohort that enrolled six children.
Patients completed assessments of functional vision and visual function at baseline, and at pre-specified follow-up periods, and are intended to be followed for a period of five years to evaluate long-term safety, efficacy and durability of response.
AAV-RPE65 was demonstrated to be generally well-tolerated after six months of follow-up, with a safety profile that was consistent with other approved and investigational ocular gene therapies. Subretinal injection targeting the central retina, including the fovea, was demonstrated to be safe and well tolerated. Retinal thinning, which has been reported in other RPE65-deficiency gene therapy studies in which the fovea was detached during subretinal injection, was not observed in this study in either adults or children.
Consistent with other ocular gene therapy dose finding trials, signs of inflammation were observed in some patients in high dose cohorts, which may have been associated with decreased activity of the AAV-RPE65 treatment in these patients. Inflammation was effectively managed and resolved with a standard steroid protocol.
In the Phase 1/2 study, across all cohorts, a statistically significant improvement in functional vision at six months versus baseline was demonstrated in the treated eye compared to the untreated control eye, as measured by the change in vision-guided mobility testing across a broad range of controlled light levels (1 lux, 4 lux, 16 lux, 64 lux and 256 lux). The mobility test assessed ability to complete navigation tasks that represent real-world visually-guided activities of daily living.1
- Across the Phase 1/2 study a statistically significant improvement in the time taken to navigate a maze was demonstrated across the full spectrum of light levels tested (n=14)2 (p=0.0017).
- A statistically significant improvement in time taken to navigate a maze was also demonstrated in the subset of patients treated at 1×1011 vg/ml (n=9), that included both the adults (Cohort 1) and all children treated (p=0.0039).
- Across the Phase 1/2 study a statistically significant improvement in the time taken to navigate a straight path was demonstrated across the full spectrum of light levels tested (n=14)3 (p=0.0107).
- A statistically significant improvement in time taken to navigate a straight path was also demonstrated in the subset of patients treated at 1×1011 vg/ml (n=9), that included both the adults (Cohort 1) and all children treated (p=0.0078).
- Mobility testing improvement from baseline was greatest at the lower light levels.
As the retina degenerates in RPE65-deficiency, patients experience progressive visual field loss. To measure visual field sensitivity, Octopus 900 full-field static perimetry was employed, and the hill of vision was calculated to determine overall change in retinal sensitivity following intervention.4
- Statistically significant improvement in retinal sensitivity at six months compared to baseline was demonstrated in the treated eye compared to the untreated control eye in adults and children treated at 1×1011 vg/ml (n=8)5 (p=0.0078).
- Greater improvements in retinal sensitivity were observed in children (n=5) than adults, most likely due to the increased preservation of the retina in younger patients (p=0.00625).
Improvements in the following visual function assessments (visual acuity and contrast sensitivity) suggest that foveal cone function improved over the 6-month follow up period in children and adults treated at the 1×1011 vg/ml dose.
As the retina degenerates in RPE65-deficiency, visual acuity declines, and is particularly reduced at late stages of disease as central vision is affected. Visual acuity was assessed by the Early Treatment of Diabetic Retinopathy Study (ETDRS) vision chart.
- Statistically significant improvement was demonstrated in the ETDRS letter score from baseline to six months in the treated eye compared to the untreated control eye in adults and children treated at 1×1011 vg/ml (n=9). A median improvement of 4.3 letters was seen across all patients treated at this dose (p=0.0156).
- This effect was greater in the pediatric patients (n=6), who had less retinal degeneration compared to the adults. A median improvement of 5.3 letters was observed in the treated versus untreated control eyes in children (p=0.0313).
RPE65-deficient patients experience poor contrast sensitivity, even at a young age. Contrast sensitivity was measured by the Pelli-Robson assessment.
- Statistically significant improvement in contrast sensitivity was demonstrated in adults and children treated at 1×1011 vg/ml (n=8)6 (p=0.0156).
Due to the favorable safety and strong activity profile established across adults and children treated with 1×1011 vg/ml in the Phase 1/2 trial, MeiraGTx has selected this dose for centrally targeted administration in a future pivotal trial.
AAV-RPE65 is a novel second-generation gene therapy candidate in development for the treatment of patients with RPE65-deficiency, a condition that causes severe sight impairment beginning at birth. Delivered via subretinal injection, AAV-RPE65 is designed to deliver a normal copy of the RPE65 gene, which is essential for photoreceptor function in the eye. AAV-RPE65 has been granted orphan designation by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of Leber congenital amaurosis (LCA) caused by disease-causing variants in the RPE65 gene. The FDA has also granted AAV-RPE65 rare pediatric disease designation for the treatment of inherited retinal dystrophy due to biallelic RPE65 disease-causing variants.
RPE65-deficiency is a rare, genetic disorder caused by disease-causing variants in the RPE65 gene. Due to rod photoreceptor dysfunction, RPE65-deficiency causes impaired vision from birth and results in the degeneration of the entire retina over time. Most RPE65-deficient patients experience poor vision in low-light conditions from a young age and suffer from central vision loss that progresses to complete blindness by early adulthood.
RPE65-deficiency is often characterized as a specific subtype of LCA caused by disease-causing variants in the RPE65 gene (LCA2), or a specific subtype of Retinitis Pigmentosa (RP) caused by disease-causing variants in the RPE65 gene (RP20).
RPE65-deficiency occurs in approximately one in 125,000 people in the U.S.7 There are estimated to be approximately 6,000 RPE65-deficient patients in the U.S., Japan and EU5, with almost 30% of those patients under the age of 30 years old. Approximately 50 new cases are diagnosed annually.
1 Functional vision was assessed by the RPE65-deficiency
mobility test. This assessment was developed and validated specifically
to measure functional vision in RPE65-deficient patients and is
accordingly responsive to changes in peripheral vision and ambient
illumination. It is a standardized, reliable and valid assessment.
(Rubin GS. Visually Guided Mobility in Patients Treated with Gene
Therapy for Leber’s Congenital Amaurosis. Investigative Ophthalmology & Visual Science. April 2010)
2 One adult patient did not complete 24-week efficacy assessments
3 One adult patient did not complete 24-week efficacy assessments
4 Weleber RG. VFMA: Topographic Analysis of Sensitivity Data from Full-Field Static Perimetry. Translational Vision Science & Technology.April 2015
5 One pediatric patient was unable to complete static perimetry testing
6 One pediatric patient was unable to complete contrast sensitivity testing
7 Based on an estimated prevalence of approximately one in 500,000 people in the U.S. with LCA related to disease-causing variants in the RPE65 gene, and approximately one in 70,000 people in the U.S. with RP due to disease-causing variants in the RPE65 gene.
MeiraGTx (NASDAQ:MGTX) is a vertically integrated, clinical stage gene therapy company with five programs in clinical development and a broad pipeline of preclinical and research programs. MeiraGTx has core capabilities in viral vector design and optimization and gene therapy manufacturing, as well as a potentially transformative gene regulation technology. Led by an experienced management team, MeiraGTx has taken a portfolio approach by licensing, acquiring and developing technologies that give depth across both product candidates and indications. MeiraGTx’s initial focus is on three distinct areas of unmet medical need: inherited retinal diseases, neurodegenerative diseases and severe forms of xerostomia and xerophthalmia. Though initially focusing on the eye, central nervous system and salivary gland, MeiraGTx intends to expand its focus in the future to develop additional gene therapy treatments for patients suffering from a range of serious diseases.
This article was written using materials from Meira’s press release.