Lysogene: A Pivotal Year 2019 for Lysogene’s MPS IIIA Phase 2-3 Clinical Trial

PARIS--(BUSINESS WIRE)-- Regulatory News:

Lysogene (FR0013233475 – LYS) (Paris:LYS), a pioneering biopharmaceutical company specializing in gene therapy targeting central nervous system (CNS) diseases, today announced major advancements, for their Sanfilippo syndrome type A (MPS IIIA) clinical program.

“Having launched our Phase 2-3 clinical trial in MPS IIIA, enrolled half of the intended study population and completed our two-year natural history study to be used as the control group, so far 2019 has been a year of significant progress. MPS IIIA is a devastating disease in young children, for which there is no currently approved treatment option. Lysogene, our partner Sarepta and the patient and physician commitment and investment to deliver potentially transformative therapies to these patients is unparalleled,” said Karen Aiach, Founder, Chairman and Chief Executive Officer.

First half 2019 MPS IIIA clinical developments

Enrollment momentum in ongoing Phase 2-3 AAVance study in MPS IIIA. The AAVance study is now underway with seven patients treated, an additional three patients enrolled and is on track to achieve full inclusion of 20 patients by H1 2020. Significant enthusiasm from MPS IIIA patient and physician communities continues.

Completion of two-year natural history study in MPS IIIA. Rigorously collected data using robust assessment tools for the primary cognitive endpoint, will be pooled with previously published data, and serve as the control arm for the ongoing pivotal Phase 2-3 trial.

Launch of PROVide, an innovative approach to record and measure treatment effects post gene therapy in the Phase 2-3 study. As a company whose origins come from within the MPS IIIA community, Lysogene has always put patients and families at the heart of their therapy development. In this effort, Lysogene has designed a study that includes qualitative interviews with caregivers about change after treatment and home-based smart phone video capture documenting the children’s progression on hallmarks of the disease. This will be a unique and valuable adjunct to the Phase 2-3 clinical efficacy data package intended to support LYS-SAF302 registration, pricing and reimbursement.

Lysogene will continue to communicate on LYS-SAF302 clinical progress throughout the coming months.

About Lysogene

Lysogene is a gene therapy company focused on the treatment of orphan diseases of the central nervous system (CNS). The company has built a unique capability to enable a safe and effective delivery of gene therapies to the CNS to treat lysosomal diseases and other genetic disorders of the CNS. A phase 2-3 clinical trial in MPS IIIA in partnership with Sarepta Therapeutics, Inc. is ongoing and a phase 1-2 clinical trial in GM1 Gangliosidosis is in preparation. In accordance with the agreements signed between Lysogene and Sarepta Therapeutics, Inc., Sarepta Therapeutics, Inc. will hold exclusive commercial rights to LYS-SAF302 in the United States and markets outside Europe; and Lysogene will maintain commercial exclusivity of LYS-SAF302 in Europe. Lysogene is also collaborating with an academic partner to define the development strategy for the treatment of Fragile X syndrome, a genetic disease related to autism. www.lysogene.com.

Lysogene’s forward-looking statements

This press release may contain forward-looking statements, especially on the Company’s progress of its Phase 2/3 clinical trial. Although the Company believes that its expectations are based on reasonable assumptions, any statements other than statements of historical facts that may be contained in this press release relating to future events are subject to (i) change without notice, (ii) factors beyond the Company’s control and (iii) the Company’s financial capabilities. These statements may include, but are not limited to, any statement beginning with, followed by or including words or phrases such as “objective”, “believe”, “anticipate”, “foresee”, “aim”, “intend”, “may”, “anticipate”, “estimate”, “plan”, “project”, “will”, “may”, “probably”, “should”, “could” and other words and phrases of the same meaning or used in negative form. Forward-looking statements are subject to inherent risks and uncertainties beyond the Company’s control that may, if any, cause actual results, performance or achievements to differ materially from those anticipated or expressed explicitly or implicitly by such forward-looking statements. A list and description of these risks, contingencies and uncertainties can be found in the documents filed by the Company with the Autorité des Marchés Financiers (AMF) pursuant to its regulatory obligations, including the Company’s 2018 registration document, registered with the AMF on 29 April 2019 under number R. 19-016, as well as in the documents and reports to be published subsequently by the Company. In addition, these forward-looking statements speak only as of the date of this press release. Readers are cautioned not to place undue reliance on these forward-looking statements. Except as required by law, the Company does not undertake any obligation to publicly update these forward-looking statements or to update the reasons why actual results could differ materially from those anticipated by the forward-looking statements, including in the event that new information becomes available. The Company’s update of one or more forward-looking statements does not imply that the Company will make any further updates to such forward-looking statements or other forward-looking statements.

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