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Precision BioSciences Says Safety Board Clears Further Dosing In Phase 1/2 PBGENE-DMD Duchenne Trial After No Serious Adverse Events In First Patient

Nov 5, 2026 · 07:18 AM ET· updated 2h ago

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Why It Matters

Precision BioSciences got permission to treat more patients in a medical trial. The first patient did not have serious side effects, which is a good early sign.

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Source: Benzinga · Read the original report at the publisher. Headline and figures shown for context; data may be delayed.

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