Harmony Biosciences Presents Promising Open-Label Extension Data of ZYN002 in Fragile X Syndrome
Data to be Presented at the Hot Topics in Child Neurology Podium Presentation Session at the American Academy of Neurology Annual Meeting
The data will be shared during a podium presentation at the
“The acceptance of our Fragile X syndrome OLE data as a podium presentation at AAN underlines the significant unmet need in FXS, and the potential for ZYN002 to become the first-and-only approved treatment for this condition,” said
Participants entered the OLE trial from the Phase 2/3 CONNECT-FX trial, and the Phase 1/2 FAB-C signal detection open-label trial. Participants in the OLE trial demonstrated clinically meaningful improvements in behavioral symptoms as measured by the Aberrant Behavior Checklist – Community (ABC-CFXS Irritability). This included participants who received active treatment in the double-blind, placebo-controlled CONNECT-FX trial, and those who transitioned from placebo to treatment in the OLE. More than 60% of participants in both groups achieved clinically meaningful improvement of at least 9 points on the ABC-CFXS Irritability scores at two consecutive visits.
Additionally, 40.6% of participants who received active treatment in the CONNECT-FX trial were rated by their caregivers as demonstrating a clinically meaningful improvement in behavior based on the Caregiver Global Impression of Change (CaGI-C) scores, compared to 29.8% who received placebo in the CONNECT-FX trial. After three years, 73.3% of patients who continued on ZYN002, as well as 72% who transitioned from placebo to ZYN002, experienced clinically meaningful improvements.
Serious treatment-emergent adverse events were reported in 4.6% of patients in the OLE, with discontinuation occurring in 3.3% of patients. Treatment-related adverse events were observed in 12.9% of patients, none of which were serious, and the most common of these adverse events was pain at the treatment application site in 6.7% of patients.
The data presented at AAN covers the period from
ZYN002 is currently being evaluated as an investigational treatment for FXS in the RECONNECT study, a Phase 3 randomized, double-blind, placebo-controlled registrational trial evaluating the safety and efficacy of ZYN002 in patients with FXS ages 3 to under 30 years. ZYN002 is not approved by the FDA for the treatment of FXS.
About ZYN002
ZYN002 is the first-and-only pharmaceutically manufactured synthetic cannabidiol devoid of THC and formulated as a patent-protected permeation-enhanced gel for transdermal delivery through the skin and into the circulatory system. The product is manufactured through a synthetic process in a cGMP facility and is not extracted from the cannabis plant. ZYN002 does not contain THC, the compound that causes the euphoric effect of cannabis, and has the potential to be a nonscheduled product if approved. Cannabidiol, the active ingredient in ZYN002, has been granted Orphan Drug Designation by the
About Fragile X Syndrome
Fragile X syndrome (FXS) is a rare genetic disorder that is the leading known inherited cause of both intellectual disability and autism spectrum disorder. The disorder negatively affects synaptic function, plasticity and neuronal connections, and results in a spectrum of intellectual disabilities and behavioral symptoms, such as social avoidance and irritability. While the exact prevalence is unknown, upwards of 80,000 patients in the
FXS is caused by a mutation in FMR1, a gene which modulates a number of systems, including the endocannabinoid system, and most critically, codes for a protein called FMRP. The FMR1 mutation manifests as multiple repeats of a DNA segment, known as the CGG triplet repeat, resulting in deficiency or lack of FMRP. FMRP helps regulate the production of other proteins and plays a role in the development of synapses, which are critical for relaying nerve impulses, and in regulating synaptic plasticity. In people with full mutation of the FMR1 gene, the CGG segment is repeated more than 200 times, and in most cases causes the gene to not function. Methylation of the FMR1 gene also plays a role in determining functionality of the gene. In approximately 60% of patients with FXS, who have complete methylation of the FMR1 gene, no FMRP is produced, resulting in dysregulation of the systems modulated by FMRP.
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