Alkeus Announces Interim TEASE-3 Study Results Evaluating Gildeuretinol in Early-Stage Stargardt Patients
Alkeus Pharmaceuticals announced positive interim data from its TEASE-3 study demonstrating that additional early-stage Stargardt disease patients treated with oral gildeuretinol acetate showed no disease progression, including stable visual acuity, over multiple years.
“These dramatic results showing preservation of vision in early-stage patients highlight the potential of gildeuretinol to prevent children diagnosed with Stargardt disease from progressing to severe vision loss when therapy is started early,” Michel Dahan, President and CEO of Alkeus Pharmaceuticals, said in a companhy news release. “Alkeus is poised to transform the treatment of Stargardt disease, a rare and relentlessly progressive condition that leads to irreversible blindness in children and adults. With no approved treatment currently available, there is an urgent need to bring an option to patients. We plan to submit an NDA to the US Food and Drug Administration for gildeuretinol as a treatment for Stargardt disease as soon as possible in 2025 based on compelling data generated to date from our multi-study clinical program.”
Alkeus will present the data at 4:30 pm PST on January 14 during the J.P. Morgan Healthcare Conference at The Westin St. Francis San Francisco, Mission Bay room, 32nd floor of the Tower Building.
“Two additional patients have completed 24 months of treatment in the TEASE-3 study, and the results demonstrated that once-daily oral gildeuretinol prevented progression and vision remained stable with a consistent, well-tolerated safety profile,” said Seemi Khan, MD, MBA, Chief Medical Officer at Alkeus Pharmaceuticals. “In addition, the initial three participants who completed the study and remained on treatment for multiple years have continued to show no progression with the longest duration of therapy to date of more than seven years. These are extremely encouraging results that provide increased understanding of gildeuretinol’s potential to preserve sight. It is challenging to identify and enroll early-stage patients before they develop symptoms, and we are grateful to these patients and their families for participating in this study.”
TEASE-3, the first clinical trial in early-stage Stargardt disease, is an open-label study of gildeuretinol. Participants have early signs of disease visible on retinal imaging but have not begun experiencing symptoms of vision loss. Fundus autofluorescence (FAF) imaging and other outcome measures are used to assess the extent to which gildeuretinol affects disease progression. Year-over-year progression is assessed, and the primary endpoint is a measure of progression after the first two years of treatment. Following the initial two-year treatment, patients can continue to receive gildeuretinol as part of an extension study. TEASE-3 has enrolled a total of seven patients to date.
About the TEASE Program
The Tolerability and Effects of ALK-001 on Stargardt diseasE (TEASE) studies consist of four independent clinical studies of oral gildeuretinol (ALK-001) in Stargardt disease, denoted as TEASE-1, TEASE-2, TEASE-3 and TEASE-4. The TEASE-1 study was a randomized, double-masked, placebo-controlled trial in 50 patients with Stargardt disease. Gildeuretinol met its prespecified primary efficacy endpoint showing a 21.6% reduction in the growth rate of retinal atrophic lesions area (square root) (P<0.001), and a 29.5% reduction for untransformed areas of retinal atrophic lesions against untreated patients. Gildeuretinol was well-tolerated. The TEASE-2 trial is an ongoing, fully enrolled, randomized, double-masked, placebo-controlled trial in 80 patients with moderate Stargardt disease, expected to read out topline data in 2025. TEASE-3, the first clinical trial in early-stage Stargardt disease, is an open-label study of gildeuretinol in genetically confirmed patients with early signs of disease visible on retinal imaging, but who have not begun experiencing symptoms of vision loss. TEASE-4 is an open-label extension study.