Tenaya Therapeutics (TNYA) announced that the first patient has been dosed with TN-401 gene therapy in the RIDGE-1 Phase 1b clinical trial at the University of California, San Francisco. Tenaya currently anticipates sharing initial data from the RIDGE-1 trial in 2025. TN-401 is being developed for the treatment of arrhythmogenic right ventricular cardiomyopathy caused by mutations in the plakophilin-2 gene. The first dose of TN-401 being assessed in the RIDGE-1 clinical trial is 3E13 vg/kg, a dose that was associated with near maximal efficacy in preclinical studies. The first three patients will be dosed on a sequential basis. Once three patients have been dosed at the 3E13 vg/kg level, a panel of independent safety reviewers will advise on plans to dose escalate and/or expand enrollment of the initial cohort dosing in parallel.
Invest with Confidence:
- Follow TipRanks' Top Wall Street Analysts to uncover their success rate and average return.
- Join thousands of data-driven investors – Build your Smart Portfolio for personalized insights.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on TNYA:
- Tenaya Therapeutics Reports Q3 2024 Progress and Financial Results
- Tenaya Therapeutics reports inducement grants under Nasdaq listing rule
- Tenaya Therapeutics price target raised to $18 from $16 at Canaccord
- Tenaya Therapeutics reports Q3 EPS (30c), consensus (37c)
- Morgan Stanley Predicts Up to 670% Jump for These 2 ‘Strong Buy’ Stocks