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home / news releases / TNYA - Tenaya Therapeutics gets U.S. FDA clearance for starting human trial of heart failure treatment


TNYA - Tenaya Therapeutics gets U.S. FDA clearance for starting human trial of heart failure treatment

  • Tenaya Therapeutics ( NASDAQ: TNYA ) said the U.S. Food and Drug Administration had cleared its application to begin clinical testing of TN-301 to potentially treat heart failure with preserved ejection fraction (HFpEF).
  • ( TNYA ) rose 3.1% before the bell.
  • Tenaya has begun its first-in-human Phase 1 clinical trial of TN-301 in healthy adult participants.
  • HFpEF is a complex disease that involves systemic inflammation, left ventricular hypertrophy, fibrosis, and diastolic dysfunction factors, and is estimated to affect more than three million people in the U.S. alone.
  • In Stage 1, participants will receive single ascending doses (SAD) of either TN-301 or placebo.

For further details see:

Tenaya Therapeutics gets U.S. FDA clearance for starting human trial of heart failure treatment
Stock Information

Company Name: Tenaya Therapeutics Inc.
Stock Symbol: TNYA
Market: NASDAQ
Website: tenayatherapeutics.com

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