Policy & Regulation
GenSight Biologics Reports Positive Follow-up Results at Week 72 of the RESCUE Phase III Clinical Trial of GS010 in Leber Hereditary Optic Neuropathy
18 April 2019 - - French biopharma company GenSight Biologics (PAR: SIGHT) has received positive results from the second scheduled readout, at Week 72, of the RESCUE Phase III clinical trial evaluating the safety and efficacy of a single intravitreal injection of GS010 (rAAV2/2-ND4) in 39 subjects whose visual loss due to 11778-ND4 Leber Hereditary Optic Neuropathy occurred up to 6 months prior to study treatment, the company said.

These subjects received GS010 in one eye and a sham injection in the other eye, with drug treatment randomized between best- and worst-affected eyes.

The key measure of visual function best-corrected visual acuity continued to improve at Week 72 compared to Week 48, demonstrating sustained recovery from the lowest point, or nadir, experienced in the acute phase of the disease.

By Week 72, GS010-treated eyes improved by -0.413 LogMAR (+21 ETDRS letters equivalent) from nadir, compared to the Week 48 improvement of -0.257 LogMAR (+13 ETDRS letters equivalent).

This recovery at week 72 could not yet completely offset deterioration from baseline through the acute phase: GS010-treated eyes were still below baseline by 0.192 LogMAR (-10 ETDRS letters equivalent), compared to 0.380 LogMAR (-19 ETDRS letters equivalent) at Week 48.

Figure 1. Time Course Visual Acuity, Change from Baseline to Week 72 in ETDRS Letters Equivalent in RESCUE
Consistent with all readouts so far in the RESCUE and REVERSE trials, sham-treated eyes had a BCVA evolution that closely tracked that of GS010-treated eyes.

At Week 72 of RESCUE, sham-treated eyes improved by -0.435 LogMAR from nadir (+21.7 ETDRS letters equivalent). The U-shaped curve thus closely matched that of GS010-treated eyes, so a statistically significant difference in visual acuity between GS010- and sham-treated eyes could not be shown.

The strength of the bilateral recovery shifted the mean BCVA in both sets of eyes from being off-chart at Week 48 to on-chart at Week 72.

In addition, 40% of GS010- and sham-treated eyes improved by a clinically meaningful difference of -0.3 LogMAR (+15 letters ETDRS) from nadir. Similarly, 58% of GS010-treated and 50% of sham-treated eyes improved by a clinically meaningful difference of -0.2 LogMAR (+10 lett ETDRS) from nadir.

Note: As per Statistical Analysis Plan, nadir was defined as the lowest post-treatment LogMAR value up to week of
interest. Light Perception/No Light Perception, or LP/NLP, vision was not included in the analysis.
Contrast sensitivity, a second visual function, evolved in a manner similar to BCVA: while values for GS010-treated eyes and sham-treated eyes remained below baseline, CS also recovered so that the gap to baseline diminished at Week 72 compared to Week 48.

The two sets of eyes closely matched each other, so that the difference between their CS values was not statistically significant.

One difference between results from the REVERSE and RESCUE trials of GS010 lies in anatomic findings.

The data so far do not indicate differential protection for the anatomy of GS010-treated eyes: in both drug-treated and sham-treated eyes, the relevant anatomy, as shown by various OCT measurements (tRNFL thickness, PMB thickness, GCL volume), continued to thin at Week 72, although the rate of thinning decreased between Week 48 and Week 72.

Among the OCT measures in the trial at Week 72, the ETDRS macular volume showed a difference between GS010-treated and sham-treated eyes (0.096 mm3, p = 0.0012).

Based on preliminary analysis of the safety data, GS010 was well-tolerated through 72 weeks.

There were no serious ocular adverse events or discontinuations due to ocular issues. The most frequently seen ocular adverse events were related to the injection procedure itself.

Transient elevations of intraocular pressure were occasionally seen but secondary to intraocular inflammation likely due to administration of GS010.

Such episodes were without sequelae and responded to conventional treatment. There were no systemic serious adverse events or discontinuations related to study treatment or study procedure.

RESCUE subjects will be evaluated again at 96 weeks, and then data will be unmasked, allowing more detailed subject-level analyses to be conducted. Results from RESCUE at Week 96 are expected to be available by the end of Q3 2019. Week 96 data from the REVERSE trial are expected earlier, in May 2019.

The third interventional study for GS010, REFLECT, is a randomized, double-masked, placebo-controlled Phase III trial evaluating the safety and efficacy of bilateral injections of GS010 in patients up to one year from onset of vision loss due to LHON. The first patient in REFLECT was treated in March 2018.

The company will host a conference call TODAY, April 17, 2019, at 10am CEST in French, and at 2.30pm CEST (8.30am EST) in English, to discuss these results.

GenSight Biologics is a clinical-stage biopharma company focused on discovering and developing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders.

The company's pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence and optogenetics to help preserve or restore vision in patients suffering from blinding retinal diseases.

GenSight Biologics' lead product candidate, GS010, is in Phase III trials in Leber Hereditary Optic Neuropathy, a rare mitochondrial disease that leads to irreversible blindness in teens and young adults.

Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to affected eyes by intravitreal injection to offer patients a sustainable functional visual recovery.