NT-501 Cell Therapy Slows Degeneration in Macular Telangiectasia
NT-501 previously received orphan drug and fast track status from the FDA and Neurotech will pursue approval in late 2022.
This content originally appeared on our sister site, Modern Retina.
Data from a phase 2 study (NCT01949324) of the NT-501 implant containing ciliary neurotrophic factor (CNTF) suggest that the treatment is efficacious in slowing neurodegeneration in macular telangiectasia type 2.1
An increase in the area of the ellipsoid zone loss was used to measure disease progression in patients with MacTel type 2. The mean (standard error) area of photoreceptor loss increased 0.27±0.05 mm2 from baseline to 24 months in the sham group compared with 0.22±0.05 mm2 from baseline to 24 months in the implant group in the ITT analyses. The eyes receiving sham treatment showed 31% greater progression of neurodegeneration. than the CNTF-treated eyes. The difference in mean (standard error) area of photoreceptor loss was 0.05±0.03 mm2 (P <.04) at 24 months.
Idiopathic macular telangiectasia type 2 (MacTel type 2) is a rare, bilateral, slowly progressive, macular degenerative disease, typically diagnosed in middle age. It is primarily a neurodegenerative disease, but also affects Müller glia, retinal pigment epithelial cells, and blood vessels.2
Although it rarely results in total blindness, MacTel type 2 is associated with blurred and distorted vision, and therefore has a serious impact on patients’ quality of life. Central vision loss, caused by retinal atrophy can occur in late stages while neovascular complications may occur at any stage. There is currently no known effective therapy.
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Neurotech Pharmaceuticals, Inc. has created genetically engineered cell lines that can be customized to produce various therapeutic proteins through its proprietary encapsulated cell technology (ECT) platform. Neurotech’s NTC-200 cell line is derived from normal human retinal pigment epithelial cells and thrives under low oxygen and low nutrient conditions making it particularly amenable to genetic manipulation under stringent selection methods.
The cell line can be genetically engineered to produce clinically relevant levels of therapeutic protein through a versatile, implantable drug delivery platform designed for long-term drug delivery. This novel cell-based delivery system has received Orphan Drug and Fast Track status from the FDA for MacTel type 2.
The phase 2 study enrolled 67 patients (99 eyes) at 11 sites and randomized eyes to receive the NT-501 Implant containing CNTF or a sham procedure. The primary endpoint was a change in a loss of photoreceptors in a well-defined area (ellipsoid zone) of the retina from baseline to month 24, as measured by spectral-domain optical coherence tomography (SD-OCT).
Neurotech has a unique partnership with the Lowy Family Group (LFG) and Lowy Medical Research Institute (LMRI). LMRI is a private, non-profit biomedical research organization dedicated to the study of MacTel type 2. Established in 2005, by LFG, LMRI’s mission is dedicated to preventing vision loss in people with MacTel type 2.
LMRI maintains the world’s largest MacTel type 2 patient registry, performs MacTel type 2-related natural history studies, and pursues important basic science, preclinical, and clinical research opportunities. Their goal is identify the cause(s) of MacTel and to ultimately contribute to the development of new therapies for patients with MacTel type 2.
It has been estimated that MacTel type 2 afflicts up to 1 in 1,000 individuals, although the incidence is likely to be higher due to difficulty in diagnosis.3,4 Most patients are diagnosed in their 40’s and 50’s; both eyes are typically affected, resulting in deterioration of central vision over a period of 10 to 20 years.5
Schematic of NT-501 Implant residing in the vitreous. Stable, endogenous secretion of the therapeutic protein assures that the availability of the protein at the target site is not only continuous but also long-term.
The NT-501 Implant consists of genetically modified human retinal pigment epithelium cells, encapsulated in a semipermeable hollow fiber membrane, that release ciliary neurotrophic factor (CNTF) into the vitreous cavity. Previous data from several hundred patients showed that the treatment was well tolerated with a good safety profile and sustained activity over many years.
In post hoc analyses, an overlay of the microperimetry data onto the en face image of the SD-OCT EZ area loss was performed. Aggregate retinal sensitivity loss, the absolute difference relative to the background sensitivity, was calculated at each test point within the area of the EZ defect and these differences were summed.
Aggregate retinal sensitivity loss (expressed in decibels) thus reflected the EZ defect area and scotoma depth in a single variable. In both groups, there was an increase in sensitivity loss over the 24-month observation period. In the per protocol population, the increase in aggregate sensitivity loss was significantly lower in the NT-501 Implant eyes as compared with the sham control eyes at Month 24 (mean difference between groups: 24.4 dB; P = .002).
In general, the NT-501 Implant was well tolerated, consistent with previous studies of the NT-501 Implant in eyes affected by retinitis pigmentosa and dry age-related macular degeneration. No participants had the implant removed during the study.
Based on these positive results, a pair of Phase 3 studies of the NT-501 Implant, for treatment of MacTel type 2, have been initiated at 42 centers and are now fully enrolled (NCT03319849 and NCT03316300). These consist of two 112-patient multicenter, sham-controlled studies.
Treatment effects will be assessed when all subjects have completed the 24-month time point. The primary endpoint is the same as in Phase 2, the rate of change of ellipsoid zone disruption. The secondary endpoints include the change in aggregate sensitivity of microperimetry within the area of ellipsoid zone disruption, reading speed, NEI Visual Function Questionnaire, and safety.
NT-501 was previously granted fast-track status by the FDA. Neurotech expects the last study visits to occur in Q3 2022 and plans to submit a Biologics License Application to the FDA in Q4 2022.
The NT-501 Implant is also being studied by Neurotech to test the neuroprotective effects of CNTF on glaucoma and is currently being tested in a randomized, sham controlled, double masked phase 2 study in 54 patients. The glaucoma study is independent of the MacTel research project.
