TN-201 is Tenaya’s potential first-in-class adeno-associated virus (AAV)-based gene therapy designed to deliver a working, full-length copy of the human MYBPC3 gene to heart muscle cells. The working MYBPC3 gene is intended to restore normal levels of myosin-binding protein, which regulates the contraction and relaxation of the heart muscle. In preclinical studies, TN-201 halted disease progression and demonstrated significant and durable disease reversal and survival benefit following a single dose.
“MYBPC3 gene mutations are the most common genetic cause of HCM and people with MYBPC3-associated HCM are at increased risk for accelerated decline and serious complications associated with their condition,” said
The MyPeak-1 Phase 1b clinical trial is a multi-center, open-label, dose-escalating study designed to assess the safety, tolerability and clinical efficacy of a one-time intravenous infusion of TN-201. The trial will initially seek to enroll at least six symptomatic (New York Heart Association Class II or III) adults who have been diagnosed with MYBPC3-associated nonobstructive HCM and have an implantable cardioverter defibrillator, and potentially treat up to 15 subjects in total from the
“The initiation of the MyPeak-1 clinical trial of TN-201 – the first gene therapy for MYBPC3-associated HCM to be studied in humans and the first of Tenaya’s gene therapy candidates to reach clinical stage – is a significant milestone in our efforts to improve patients’ lives through the development of new treatments that target the genetic underpinnings of heart disease,” said
The first dose of TN-201 being assessed in the MyPeak-1 clinical trial is 3E13 vg/kg, a dose associated with near-maximal efficacy in preclinical studies. Once three patients have been dosed at the 3E13 vg/kg level, a data safety and monitoring board (DSMB) of external advisors will review safety data and advise Tenaya on plans to enroll patients at the dose level of 6E13vg/kg and enroll additional patients in the initial dose cohort.
The MyPeak-1 clinical trial will be conducted at up to twelve leading
About MYBPC3-Associated Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder, and variants in the Myosin Binding Protein C3 (MYBPC3) gene are the most common genetic cause of HCM. MYBPC3-associated HCM is estimated to account for approximately 20 percent of the overall HCM population and to affect approximately 115,000 patients in
About TN-201
TN-201 is an investigational first-in-class adeno-associated virus (AAV)-based gene therapy being developed to treat HCM due to disease-causing variants in the MYBPC3 gene. TN-201 gene therapy is intended to deliver a working MYBPC3 gene to specific cells of the heart via a single infusion to address the underlying cause of MYBPC3-associated HCM. The
Tenaya is conducting the Phase 1b MyPeak-1 clinical trial in symptomatic adults diagnosed with MYBPC3-associated nonobstructive HCM. As safety and dosing are established, Tenaya plans to develop TN-201 for any patient with a pathogenic MYBPC3 mutation, including adults with obstructive disease and infants, children and teens with heterozygous or homozygous mutations.
A non-interventional natural history study designed to understand MYBPC3-associated HCM in infants, children and teens known as the MyClimb Natural History study is also ongoing at twenty-four sites in the
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Forward Looking Statements
This press release contains forward-looking statements as that term is defined in Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Statements in this press release that are not purely historical are forward-looking statements. Words such as “anticipates,” “potential,” “seek,” “look forward,” “will,” “plan,” and similar expressions are intended to identify forward-looking statements. Such forward-looking statements include, among other things, the expected timing for sharing initial clinical data from MyPeak-1; the clinical and therapeutic potential of TN-201 as a one-time treatment to correct the underlying genetic cause of MYBPC3-associated HCM and improve patient outcomes; enrollment targets for MyPeak-1; and clinical development plans for TN-201. The forward-looking statements contained herein are based upon Tenaya’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. These forward-looking statements are neither promises nor guarantees and are subject to a variety of risks and uncertainties, including but not limited to: the timing and progress of MyPeak-1; unexpected concerns that may arise as a result of the occurrence of adverse safety events in MyPeak-1; the potential failure of TN-201 to demonstrate safety and/or efficacy in clinical testing; the potential for MyPeak-1 initial clinical trial results to differ from preclinical or expected results; the timing, scope and likelihood of regulatory filings and approvals for TN-201; Tenaya’s ability to successfully operate a manufacturing facility for clinical supply for TN-201; risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics and operating as an early stage company; Tenaya’s ability to develop, initiate or complete preclinical studies and clinical trials, and obtain approvals, for any of its product candidates; Tenaya’s continuing compliance with applicable legal and regulatory requirements; Tenaya’s ability to raise any additional funding it will need to continue to pursue its business and product development plans; Tenaya’s reliance on third parties; Tenaya’s commercialization and marketing capabilities and strategy; the loss of key scientific or management personnel; competition in the industry in which Tenaya operates; Tenaya’s ability to obtain and maintain intellectual property protection for its product candidates; general economic and market conditions; and other risks. Information regarding the foregoing and additional risks may be found in the section entitled “Risk Factors” in documents that Tenaya files from time to time with the
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