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FDA Pauses Tenaya TN-201 Gene Therapy Trial for Standardization

The FDA placed a clinical hold on Tenaya’s TN-201 trial for MYBPC3-associated HCM to standardize immunosuppression patient management across sites. No delays expected.

FDA Pauses Tenaya TN-201 Gene Therapy Trial for Standardization
Credit: Tenaya Therapeutics
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11/10/2025 · 6:46 AM
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