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

Status: Recruiting
Location: See location...
Intervention Type: Genetic
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is intented to evaluate the safety, tolerability and preliminary efficacy of CRISPR/Cas9 Instantaneous Gene Editing Therapy (BD113 virus-like particle, also BD113vLVP) in patients with primary open-angle glaucoma (POAG) with elevated intraocular pressure and MYOC gene mutation. The main objectives to evaluate the safety and tolerability BD113vLVP) in POAG patients with intraocular hypertension and MYOC mutation, and secondary objectives is to explore the preliminary efficacy and the metabolism characteristics of BD113vLVP in participants.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
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⁃ Signed ICF;

⁃ Aged 18 to 65 years old;

⁃ Primary open Angle glaucoma (POAG) with elevated intraocular pressure (IOP) was diagnosed with ≥1 year medical history record ;

⁃ Good function level of organs;

⁃ Good compliance and willing to comply with the visit schedule, laboratory tests and other specified test etc. per protocol;

⁃ Agreeing to accept a long-term safety follow-up after 1 year of study.

‣ Special Inclusion Criteria for Group 1:

• Target intervenning eye is no visual acuity;

• The intraocular pressure (IOP) was ≤35 mmHg and \> 21 mmHg after receiving a combination therapy of 2 or more drugs lowering IOP.

‣ Special Inclusion Criteria for Group 2:

• MYOC gene mutation was detected in peripheral blood nucleated cells ;

• The intraocular pressure (IOP) was ≤30 mmHg and \> 21 mmHg after receiving a combination therapy of 2 or more drugs lowering IOP;

• Both eyes have a Shaffer Angle mirror rating greater than 3.

Locations
Other Locations
China
Beijing Tongren Hospital, Capital Medical University
RECRUITING
Beijing
Contact Information
Primary
Fujun Li, M.D.
fujun.li@bdgene.cn
086-191 2131 1061
Time Frame
Start Date: 2024-06-10
Estimated Completion Date: 2025-12
Participants
Target number of participants: 9
Treatments
Experimental: Group 1: POAG without vision for interventional eye
Interventional eye of participants with POAG has no vision, with mutated or unmutated MYOC gene. Single dose of BD113vVLP will be administrated intracamerally for target interventional eye.
Experimental: Group 2: POAG with vision for interventional eye
Interventional eye of participants with POAG has vision acuity, and MYOC gene mutation test is positive. Single dose of BD113vVLP will be administrated intracamerally for target interventional eye.
Sponsors
Collaborators: Beijing Tongren Hospital
Leads: Shanghai BDgene Co., Ltd.

This content was sourced from clinicaltrials.gov