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CLINICAL_TRIALS research · 2024-06-24

Clinical Trial Update: CRISPR/Cas9 Instantaneous Gene Editing Therapy to Intraocular Hypertensive POAG With MYOC Mutation [NA]

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Summary

A CRISPR/Cas9 instantaneous gene editing therapy for MYOC-mutant primary open-angle glaucoma is in a clinical trial and currently recruiting.

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Diseases / indications

Drugs mentioned

  • CRISPR/Cas9 instantaneous gene editing therapy

Snippet

Sponsor: Shanghai BDgene Co., Ltd. | Conditions: Primary Open Angle Glaucoma | NA | Status: RECRUITING