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Tenaya Therapeutics Granted U.S. FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for TN-401 for the Treatment of PKP2-Associated Arrhythmogenic Right Ventricular Cardiomyopathy

RMAT status and encouraging interim data strengthen the regulatory path for Tenaya’s TN-401 gene therapy in PKP2-associated ARVC.

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Tenaya Therapeutics (TNYA) received U.S. FDA Regenerative Medicine Advanced Therapy (RMAT) designation for TN-401 for PKP2-associated arrhythmogenic right ventricular cardiomyopathy (ARVC) as of September 14, 2026.

The designation is supported by interim data from the Phase 1b/2 RIDGE-1 trial, which showed clinically meaningful reductions in daily rates of premature ventricular contractions (PVCs) and non-sustained ventricular tachycardias (NSVTs), along with a favorable tolerability profile. Tenaya plans to share additional RIDGE-1 data and provide an update on regulatory discussions about a potential pivotal trial for TN-401 in the fourth quarter of 2026. TN-401 is an investigational AAV9-based, one-time intravenous gene therapy for PKP2-associated ARVC and already holds U.S. Orphan Drug and Fast Track designations, as well as EMA PRIME designation, and is supported in part by a grant from the California Institute for Regenerative Medicine.

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Positive

  • TN-401 granted FDA RMAT designation for PKP2-associated ARVC
  • Interim RIDGE-1 data show reduced daily PVC and NSVT rates with favorable tolerability
  • TN-401 also holds Orphan Drug, Fast Track and EMA PRIME designations
  • Development of TN-401 supported in part by a CIRM grant
  • Additional RIDGE-1 data and pivotal-trial regulatory update expected in 4Q 2026

Negative

  • None.

News Explained

Tenaya has received FDA RMAT designation for TN-401, a development-stage milestone that adds opportunities for early and ongoing FDA guidance on clinical development, manufacturing and potential regulatory pathways, with possible eligibility for accelerated, priority or rolling review.

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Market Reaction – TNYA

$0.65 $0.65 Day Range
$146.51M Market Cap

Following this news, TNYA has gained 2.09%, reflecting a moderate positive market reaction. The stock is currently trading at $0.65. Trading volume is elevated at 2.9x the average, suggesting notable buying interest.

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Market Context

TNYA was down 1.36% before publication, while the Aug 05 RIDGE-1 update saw a 7.51% 24-hour decline;...
Analysis

TNYA was down 1.36% before publication, while the Aug 05 RIDGE-1 update saw a 7.51% 24-hour decline; the RMAT designation added a regulatory milestone to the same program.

Key Figures

Additional data and regulatory update: 4Q 2026 Planned enrollment: Up to 15 adults
Additional data and regulatory update
4Q 2026
Expected timing for RIDGE-1 data and pivotal-trial discussions
Planned enrollment
Up to 15 adults
RIDGE-1 Phase 1b/2 trial

Historical Context

1 past event · Latest: Aug 05
1 event
  1. Aug 05

    TN-401 interim data

    24h Move
    -7.5%

    RIDGE-1 reported a mean 64% PVC reduction with no dose-limiting toxicities

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

rmat, pkp2, aav9-based gene therapy, premature ventricular contractions, +1 more
5 terms
rmat regulatory
"FDA has granted Regenerative Medicine Advanced Therapy (RMAT) designation"
A Regenerative Medicine Advanced Therapy (RMAT) designation is a regulatory fast-track status for cell, gene or tissue-based therapies that show promise for treating serious conditions. It acts like an express lane with extra support from regulators—potentially shortening review time and enabling earlier approval paths—which can reduce development risk and speed a therapy toward the market, making it a material value signal for investors in biotech stocks.
pkp2 medical
"treatment of PKP2-associated arrhythmogenic right ventricular cardiomyopathy"
PKP2 is a gene that encodes a protein functioning like cellular “glue,” keeping heart muscle cells attached and helping electrical signals travel smoothly across the heart. Changes in PKP2 can weaken that glue and lead to dangerous heart rhythm disturbances or structural heart disease, so investors monitor PKP2-related genetic tests, diagnostics and therapies because such findings can influence demand for medical products, regulatory reviews and company valuations.
aav9-based gene therapy technical
"TN-401 is an investigational AAV9-based gene therapy"
AAV9-based gene therapy uses a harmless virus called adeno-associated virus serotype 9 as a delivery vehicle to carry a therapeutic gene into a patient’s cells. Think of AAV9 as a specialized courier that can transport genetic instructions to target tissues, sometimes including the brain or nervous system, to correct or replace a faulty gene. It matters to investors because the choice of AAV9 affects clinical results, manufacturing complexity, regulatory review, and potential market size for gene therapies.
premature ventricular contractions medical
"reduced rates of premature ventricular contractions (PVCs)"
Premature ventricular contractions are extra heartbeats that begin in the heart’s lower chambers and occur earlier than the next expected beat, often experienced as a skipped beat, flutter or extra thump. For investors, they matter because frequent or symptomatic PVCs can indicate underlying heart disease or drug side effects, affecting clinical trial safety, regulatory reviews, and potential liability or treatment costs—like a dashboard warning that could change a company’s health-related risks.
non-sustained ventricular tachycardias medical
"non-sustained ventricular tachycardias (NSVTs)"
Non-sustained ventricular tachycardias are short bursts of very fast heartbeats that start in the ventricles (the heart’s lower chambers) and stop on their own within a short time. They matter to investors because they can signal underlying heart disease or treatment side effects, influencing the safety profile of drugs or devices, clinical trial outcomes, regulatory decisions and ultimately a company’s market value — think of them as brief electrical glitches that raise concern about longer-term reliability.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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RMAT Designation Supported by Positive Interim Data from RIDGE™-1 Phase 1b/2 Clinical Trial of TN-401 which Demonstrated Reduced Arrhythmia Burden 

Additional Data and Updates on Regulatory Discussions Anticipated in 4Q 2026

SOUTH SAN FRANCISCO, Calif., Sept. 14, 2026 (GLOBE NEWSWIRE) -- Tenaya Therapeutics, Inc. (NASDAQ: TNYA), a clinical-stage biotechnology company with a mission to discover, develop and deliver potentially curative therapies that address the underlying causes of heart disease, today announced that the U.S. Food and Drug Administration (FDA) has granted Regenerative Medicine Advanced Therapy (RMAT) designation to TN-401, Tenaya’s gene therapy candidate for the treatment of PKP2-associated arrhythmogenic right ventricular cardiomyopathy (ARVC).

"RMAT designation underscores the continued recognition by regulators of the seriousness of PKP2-associated ARVC and the potential of TN-401 gene therapy to change the course of disease by addressing its underlying cause. This designation is supported by the encouraging interim data generated to date from our RIDGE-1 trial, which demonstrated clinically meaningful reductions in daily rates of PVCs and NSVTs, as well as a favorable tolerability profile," said Faraz Ali, Chief Executive Officer of Tenaya Therapeutics. "Together with Fast Track and Orphan Drug designations, RMAT enhances our ability to engage with the FDA as we strive to advance TN-401 toward a pivotal trial in order to bring this potentially transformative treatment to patients as quickly as possible. We look forward to sharing additional data from RIDGE-1 in the fourth quarter and providing an update on our ongoing discussions with regulators regarding pivotal trial plans for TN-401."

Tenaya’s RMAT application included data presented at the American Society for Gene and Cell Therapy (ASGCT) Annual Meeting in May 2026. Interim results from the RIDGE-1 clinical trial of TN-401 showed improvements in multiple electrical stability measures, including reduced rates of premature ventricular contractions (PVCs) and non-sustained ventricular tachycardias (NSVTs), two of the most frequently occurring forms of ventricular arrhythmias that characterize ARVC.

RMAT designation is an FDA expedited program intended to facilitate the development and review of regenerative medicine therapies for serious conditions where preliminary clinical evidence indicates the potential to address unmet medical needs. RMAT designation provides enhanced opportunities for interaction with the FDA, including early and ongoing guidance regarding clinical development, manufacturing and potential regulatory pathways, and it may provide eligibility for accelerated approval, priority review and rolling review.

About PKP2-Associated ARVC
Plakophilin-2 (PKP2) mutations are the most common genetic cause of arrhythmogenic right ventricular cardiomyopathy (ARVC, also known as arrhythmogenic cardiomyopathy or ACM), occurring in approximately 40 percent of the overall ARVC population. The prevalence of PKP2-associated ARVC is estimated at more than 70,000 people in the U.S. alone.

In PKP2-associated ARVC, mutations of the PKP2 gene results in insufficient expression of a protein needed for the proper functioning of the desmosomal complex that maintains physical connections and electrical signaling between heart muscle cells. As the desmosome structure degrades, cardiac muscle cells are replaced by fibrofatty tissue and electrical pulses in the heart become unstable, resulting in life potentially threatening heart rhythms. ARVC symptoms include arrhythmias, palpitations, lightheadedness, dizziness and fainting. It is typically diagnosed before age 40, and sudden cardiac arrest due to ventricular arrhythmia is frequently the first manifestation of disease. Current treatments include anti-arrhythmic medications, implantable cardioverter-defibrillators (ICDs) and ablation procedures, which do not address the underlying genetic cause of disease.

About TN-401 Gene Therapy and the RIDGE-1 Clinical Trial
TN-401 is an investigational AAV9-based gene therapy being developed for the treatment of ARVC due to mutations in the PKP2 gene. AAV9 was selected as the vector for delivery of Tenaya’s PKP2 gene therapy based on its extensive clinical and commercial safety record and demonstrated ability to target heart muscle cells. TN-401 has received Orphan Drug and Fast Track Designations from the U.S. Food and Drug Administration, as well as PRIME designation from the European Medicines Agency. Tenaya’s development of TN-401 is supported in part by a grant from the California Institute for Regenerative Medicine (CIRM).

The RIDGE-1 Phase 1b/2 clinical trial ClinicalTrials.gov (NCT06228924) of TN-401 in patients with PKP2-associated ARVC is a multi-center, open-label, dose escalation study being conducted in the U.S. and UK. RIDGE-1 is intended to assess the safety, tolerability and preliminary clinical efficacy of a one-time intravenous infusion of TN-401. RIDGE-1 seeks to enroll up to fifteen adults who have been diagnosed with PKP2-associated ARVC, have an ICD and are at increased risk for arrhythmias as determined by premature ventricular count (PVC) during screening. As part of its TN-401 development program, Tenaya is also conducting RIDGE ClinicalTrials.gov (NCT06311708), believed to be the largest natural history study of adults with PKP2-associated ARVC.

To learn more about gene therapy for ARVC and the RIDGE-1 clinical trial, please visit ARVCstudies.com.

About Tenaya Therapeutics
Tenaya Therapeutics is a clinical-stage biotechnology company committed to a bold mission: to discover, develop and deliver potentially curative therapies that address the underlying drivers of heart disease. Tenaya’s pipeline includes clinical-stage candidates TN-201, a gene therapy for MYBPC3-associated hypertrophic cardiomyopathy (HCM); TN-401, a gene therapy for PKP2-associated arrhythmogenic right ventricular cardiomyopathy (ARVC); and TN-301, a highly specific small molecule HDAC6 inhibitor with broad potential clinical utility in cardiac, metabolic and muscular conditions, including heart failure with preserved ejection fraction (HFpEF) and Duchenne muscular dystrophy (DMD). Tenaya has employed a suite of integrated internal capabilities including modality agnostic target discovery and validation, to generate a portfolio of novel medicines based on genetic insights, aimed at the treatment of both rare genetic disorders and more prevalent heart conditions. For more information, visit www.tenayatherapeutics.com.

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 “anticipated,” “potential,” “strive,” “look forward,” “may” and similar expressions are intended to identify forward-looking statements. Such forward-looking statements include, among other things, the plan and related timing to share additional data from RIDGE-1 and provide an update on regulatory discussions regarding pivotal trial plans for TN-401; the potential for TN-401 gene therapy to change the course of PKP2-associated ARVC by addressing the underlying cause of disease; the potential development and regulatory review opportunities for TN-401 due to RMAT designation; Tenaya’s efforts to advance TN-401 toward a pivotal trial; and statements 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: availability of data at the referenced time; the timing and progress of RIDGE-1 and Tenaya’s other ongoing clinical trials; the potential failure of TN-401 and Tenaya’s other product candidates to demonstrate safety and/or efficacy in clinical testing; the potential for the FDA and/or other regulatory agencies to conclude at any time that TN-401 may not have an appropriate risk/benefit profile; changes in Tenaya’s plans to develop and commercialize TN-401 and its other product candidates; the potential for RIDGE-1 clinical trial results to differ from preclinical, interim, preliminary, topline or expected results; risks associated with the process of discovering, developing and commercializing therapies that are safe and effective for use as human therapeutics; 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 the clinical development of TN-401 and its other product candidates, as well as Tenaya’s general business 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 Tenaya’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2026, and future documents that Tenaya files from time to time with the Securities and Exchange Commission. These forward-looking statements are made as of the date of this press release, and Tenaya assumes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

Tenaya Contacts
Michelle Corral
VP, Corporate Communications and Investor Relations
IR@tenayathera.com

Investors
Anne-Marie Fields
Precision AQ
annemarie.fields@precisionaq.com

Media
Wendy Ryan
Ten Bridges Communications
wendy@tenbridgecommunications.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What does FDA RMAT designation provide for TN-401 development?

RMAT designation is an FDA expedited program for regenerative medicines for serious conditions with preliminary clinical evidence of potential to address unmet medical needs. For TN-401, it provides enhanced opportunities for interaction with the FDA, including early and ongoing guidance on clinical development, manufacturing and regulatory pathways, and it may provide eligibility for accelerated approval, priority review and rolling review.

What is the design of the RIDGE-1 clinical trial of TN-401?

RIDGE-1 (NCT06228924) is a multi-center, open-label, Phase 1b/2 dose-escalation study of a one-time intravenous infusion of TN-401 in adults with PKP2-associated ARVC. It is being conducted in the U.S. and UK, aims to enroll up to fifteen adults who have an implantable cardioverter-defibrillator and are at increased arrhythmia risk based on premature ventricular contraction counts at screening, and is intended to assess safety, tolerability and preliminary clinical efficacy.

How can patients or physicians learn more about TN-401 gene therapy and RIDGE-1?

To learn more about gene therapy for ARVC and the RIDGE-1 clinical trial of TN-401 for PKP2-associated ARVC, interested parties are directed to visit ARVCstudies.com.

What other clinical-stage programs does Tenaya Therapeutics have besides TN-401?

Tenaya’s pipeline includes TN-201, a gene therapy for MYBPC3-associated hypertrophic cardiomyopathy; TN-401, a gene therapy for PKP2-associated ARVC; and TN-301, a highly specific small-molecule HDAC6 inhibitor with potential use in cardiac, metabolic and muscular conditions, including heart failure with preserved ejection fraction and Duchenne muscular dystrophy.

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