Initial Data from Ongoing MyPeak™-1 Phase 1b of TN-201 for MYBPC3-associated HCM Expected in Second Half of 2024
On Track to Dose First Patient in RIDGE™-1Phase 1b Clinical Trial of TN-401 for PKP2-associated ARVC in Second Half 2024
“Tenaya had a successful year of sustained execution in 2023 that meaningfully advanced our portfolio of genetic medicines for heart disease. We announced IND clearance for the TN-201 and TN-401 gene therapy programs; activated clinical trial sites in the
Business and Program Updates
TN-201 – Gene Therapy for MYBPC3-Associated Hypertrophic Cardiomyopathy (HCM)
- In
October 2023 , the first patient was dosed in the MyPEAK-1 Phase 1b clinical trial of TN-201 for the treatment of Myosin Binding Protein C3 (MYBPC3)-associated HCM. MyPEAK-1 is a multi-center, open-label, dose-escalation trial designed to assess safety, tolerability and clinical efficacy of a one-time intravenous infusion of TN-201.- Tenaya anticipates sharing initial safety, biopsy and biomarker data from the first cohort of patients in MyPEAK-1 trial in the second half of 2024.
- Tenaya is conducting two non-interventional studies to support the development of TN-201: MyClimb, a natural history study of pediatric patients with MYBPC3-associated HCM and a study evaluating seroprevalence to adeno-associated virus serotype 9 (AAV9) antibodies among adults with MYBPC3-associated HCM.
- In
October 2023 , Tenaya shared interim results indicating that a majority of MYBPC3-associated HCM patients could be eligible for TN-201 treatment due to low levels of preexisting neutralizing antibodies to AAV9.
- In
TN-401 – Gene Therapy for PKP2-Associated Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Tenaya is on track to begin dosing in the RIDGE-1 Phase 1b clinical trial of TN-401 in the second half of 2024. RIDGE-1 is a multicenter, open-label, dose-escalation trial designed to assess safety, tolerability and clinical efficacy of a one-time intravenous infusion of TN-401 for the treatment of ARVC caused by mutations to the Plakophilin-2 (PKP2) gene.
- In November, TN-401 received Fast Track Designation from the FDA.
- Tenaya is currently conducting a global, non-interventional seroprevalence and natural history study (RIDGE™) enrolling adult PKP2-associated ARV patients.
TN-301 – Small Molecule HDAC6 Inhibitor for Heart Failure with Preserved Ejection Fraction (HFpEF)
- At the 2023 Heart Failure Society of America Annual
Scientific Meeting inOctober 2023 , Tenaya shared positive clinical and preclinical data for its small molecule HDAC6 inhibitor program, TN-301.- Results from a Phase 1 dose-escalation study demonstrated that TN-301 was generally well tolerated across the broad range of doses studied. Pharmacokinetic (PK) results showed overall dose proportionality in the single- and multiple-ascending dose stages of the study with a half-life supportive of once-daily dosing. Robust HDAC6 inhibition was observed and increasing doses and exposures with TN-301 correlated with increased pharmacodynamic effects.
- New preclinical results demonstrated that the combination of Tenaya’s HDAC6 inhibitor with empagliflozin (a sodium-glucose cotransporter-2 inhibitor) achieved additive benefits in validated HFpEF mouse models compared to either compound alone.
Follow-on Financing
In
Fourth Quarter and Full Year 2023 Financial Highlights
- Cash Position and Guidance: As of
December 31, 2023 , cash, cash equivalents and investments in marketable securities were$104.6 million . Tenaya expects these funds, combined with net proceeds of$46.5 million from the recent financing, will be sufficient to fund the company into the second half of 2025. - Research & Development (R&D) Expenses: R&D expenses were
$22.9 million for the fourth quarter and$98.0 million for the full year endedDecember 31, 2023 . Non-cash stock-based compensation included in R&D expense was$1.8 million for the fourth quarter and$7.0 million for the full year endedDecember 31, 2023 . - General & Administrative (G&A) Expenses: G&A expenses were
$8.6 million for the fourth quarter and$33.2 million for the full year endedDecember 31, 2023 . Non-cash stock-based compensation included in G&A expense was$2.1 million for the fourth quarter and$8.3 million for the full year endedDecember 31, 2023 . - Net Loss: Net loss was
$29.9 million , or$0.40 per share for the fourth quarter endedDecember 31, 2023 . For the full year 2023, net loss was$124.1 million , or$1.68 per share.
About Tenaya Therapeutics
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 “expected,” “on track,” “look forward,” “anticipates,” “expects,” and similar expressions are intended to identify forward-looking statements. Such forward-looking statements include, among other things, Tenaya’s plans and expectations regarding its clinical development efforts and activities, including the planned timing of sharing initial data from MyPeak-1 and planned initiation of patient dosing in RIDGE-1; the clinical, therapeutic and commercial potential of, and expectations regarding, Tenaya’s product candidates; the sufficiency of Tenaya’s cash resources to fund the company into the second half 2025; and statements made by Tenaya’s chief executive officer. 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 Tenaya’s clinical trials; availability of data at the referenced times; unexpected concerns that may arise as a result of the occurrence of adverse safety events in Tenaya’s clinical trials; the potential failure of Tenaya’s product candidates to demonstrate safety and/or efficacy in clinical testing; the potential for any clinical trial results to differ from preclinical, interim, preliminary, topline or expected results; 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 manufacturing, 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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Condensed Statements of Operations (In thousands, except share and per share data) (Unaudited) | ||||||||||||||||
Three Months Ended | Year Ended | |||||||||||||||
2023 | 2022 | 2023 | 2022 | |||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | $ | 22,865 | $ | 25,748 | $ | 98,038 | $ | 94,537 | ||||||||
General and administrative | 8,581 | 8,802 | 33,155 | 31,084 | ||||||||||||
Total operating expenses | 31,446 | 34,550 | 131,193 | 125,621 | ||||||||||||
Loss from operations | (31,446 | ) | (34,550 | ) | (131,193 | ) | (125,621 | ) | ||||||||
Other income, net: | ||||||||||||||||
Interest income | 1,470 | 1,037 | 7,056 | 1,954 | ||||||||||||
Other income (expense), net | 41 | (3 | ) | 53 | 2 | |||||||||||
Total other income, net | 1,511 | 1,034 | 7,109 | 1,956 | ||||||||||||
Net loss before income tax expense | (29,935 | ) | (33,516 | ) | (124,084 | ) | (123,665 | ) | ||||||||
Income tax expense | — | — | — | — | ||||||||||||
Net loss | $ | (29,935 | ) | $ | (33,516 | ) | $ | (124,084 | ) | $ | (123,665 | ) | ||||
Net loss per share, basic and diluted | $ | (0.40 | ) | $ | (0.61 | ) | $ | (1.68 | ) | $ | (2.76 | ) | ||||
Weighted-average shares used in computing net loss per share, basic and diluted | 74,097,642 | 55,250,372 | 73,786,126 | 44,823,597 |
Condensed Balance Sheet Data (In thousands) (Unaudited) | ||||||||
2023 | 2022 | |||||||
Cash, cash equivalents and marketable securities | $ | 104,642 | $ | 204,230 | ||||
Total assets | $ | 170,515 | $ | 278,945 | ||||
Total liabilities | $ | 31,091 | $ | 35,569 | ||||
Total liabilities and stockholders’ equity | $ | 170,515 | $ | 278,945 |
Source:
2024 GlobeNewswire, Inc., source