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NCT06465537RECRUITINGanonymous

A Clinical Study on CRISPR/Cas9 Instantaneous Gene Editing Therapy to Primary Open-angle Glaucoma With Elevated Intraocular Pressure and MYOC Gene Mutation

Sponsor

Source record

Shanghai BDgene Co., Ltd.

Phase

Source record

Phase 1/2

Modality

AI-normalized

gene therapy

Target

AI-normalized

MYOC gene mutation in patients with primary open-angle glaucoma (POAG) and elevated intraocular pressure (IOP). The intervention utilizes CRISPR/Cas9 technology to edit the MYOC gene, aiming to reduce IOP.

Indication / condition

AI-normalized

Primary Open Angle Glaucoma

Intervention

Source record

BD113vVLP

Source & freshness

Source record

NCT ID

NCT06465537

Original source

ClinicalTrials.gov

Source last updated

Jun 24, 2024

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT06465537

Title

A Clinical Study on CRISPR/Cas9 Instantaneous Gene Editing Therapy to Primary Open-angle Glaucoma With Elevated Intraocular Pressure and MYOC Gene Mutation

Sponsor

Shanghai BDgene Co., Ltd.

Status

RECRUITING

Phase

Phase 1/2

Condition raw

Primary Open Angle Glaucoma

Condition normalized

Primary Open Angle Glaucoma

Modality raw

gene therapy

Modality normalized

gene therapy

Target raw

MYOC gene mutation in patients with primary open-angle glaucoma (POAG) and elevated intraocular pressure (IOP). The intervention utilizes CRISPR/Cas9 technology to edit the MYOC gene, aiming to reduce IOP.

Target normalized

MYOC gene mutation in patients with primary open-angle glaucoma (POAG) and elevated intraocular pressure (IOP). The intervention utilizes CRISPR/Cas9 technology to edit the MYOC gene, aiming to reduce IOP.

Interventions

BD113vVLP

Public preview

Source record

The trial is sponsored by Shanghai BDgene Co., Ltd. and aims to address a significant unmet medical need in the treatment of POAG, particularly in patients with MYOC mutations. The global glaucoma therapeutics market is projected to grow, driven by increasing prevalence and advancements in gene therapy. Successful outcomes could position BDgene as a leader in gene editing therapies for ocular diseases, potentially attracting partnerships or acquisitions. However, competition from established pharmaceutical companies and emerging biotech firms in the gene therapy space poses a risk. Diligence should focus on regulatory pathways, reimbursement strategies, and the robustness of clinical data.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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