[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"retinal-dystrophy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:retinal-dystrophy":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100597787","early-phase-1-a-study-of-lx107-gene-therapy-in-aipl1-ird-patients-100597787",false,"NCT07063030","A Study of LX107 Gene Therapy in AIPL1-IRD Patients","An Exploratory Clinical Study to Evaluate LX107 Gene Therapy in Patients With AIPL1 Biallelic Mutation-related Inherited Retinal Dystrophy (AIPL1-IRD)","Inclusion Criteria:\n\n1. The subject and\u002For their guardian signs a written informed consent form and is willing to comply with the long-term follow-up protocol and supporting protocols.\n2. Adult or pediatric patients (aged ≥ 4 years) diagnosed with AIPL1-IRD.\n3. Definitive molecular diagnosis of biallelic AIPL1 gene mutations confirmed by next-generation sequencing combined with Sanger validation.\n4. The study eye has a best-corrected visual acuity of no more than 58 letters (approximately equivalent to decimal visual acuity ≤ 0.3) using the ETDRS visual acuity chart at baseline.\n\nNote: Only one eye will be designated as the \"study eye\" (i.e., the eye to receive treatment) at the investigator's discretion.\n\nExclusion Criteria:For any eye with the following conditions:\n\n1. A history of ocular diseases that, in the investigator's judgment, may hinder the planned treatment or interfere with the interpretation of study endpoints (e.g., glaucoma, diabetic retinopathy, retinal vein occlusion, retinal detachment, posterior or panuveitis, etc.).\n2. Any eye with a history of gene therapy for IRD or other hereditary neuro-ophthalmic diseases (including but not limited to other viral vector-based gene therapies, mRNA therapies, etc.).\n3. A lack of sufficient viable retinal cells as determined by non-invasive methods such as OCT or ophthalmoscopy.\n4. Any active intraocular or periocular infection in the study eye (e.g., infectious conjunctivitis, keratitis, scleritis, endophthalmitis, infectious blepharitis, uveitis).\n5. A history of intraocular surgery (e.g., vitrectomy, cataract surgery, trabeculectomy, or other filtering surgery) in the 6 months prior to the screening visit.\n\n   For any systemic conditions:\n6. Uncontrolled hypertension, defined as systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg. If the initial measurement exceeds the above limits, it may be repeated on the same day or another day during the screening period; if the subject is taking oral antihypertensive drugs, they must have been on a stable dose of the same drug for at least 30 days prior to screening.\n7. Diabetic patients meeting any of the following criteria: ① known to have macrovascular complications; ② baseline HbA1c \\> 7.5%; ③ receiving treatment with two or more oral hypoglycemic agents, insulin, or GLP-1 receptor agonists.\n8. A history of any other diseases, metabolic disorders, physical examination findings, or clinical laboratory abnormalities that, in the investigator's judgment, may contraindicate the use of the study drug, interfere with the interpretation of study results, or place the subject at high risk of treatment complications, including but not limited to: AIDS, syphilis, acute\u002Fchronic active hepatitis B or C, coagulation disorders, a history of treated or untreated malignancy within the past 5 years (except for localized basal cell carcinoma of the skin or in situ cervical cancer), etc.\n9. Any of the following laboratory abnormalities: ① platelet count \\\u003C 100 × 10⁹\u002FL, hemoglobin (Hb) \\\u003C 10 g\u002FdL (males) or \\\u003C 9 g\u002FdL (females); ② aspartate aminotransferase (AST) or alanine aminotransferase (ALT) \\> 3 × ULN; ③ serum creatinine or urea \\> 1.5 × ULN.\n10. Administration of any other investigational drug (except vitamins and minerals) within 3 months prior to screening, or an attempt to participate in another clinical trial during the study period.\n11. Other circumstances deemed unsuitable for enrollment by the investigator.\n12. Unwillingness to use effective contraceptive methods during the study; pregnant or lactating women, or women planning to become pregnant or lactate during the study period.","ALL","4 Years",{"count":19,"type":20},13,"ESTIMATED","INTERVENTIONAL",[23],"EARLY_PHASE1","Administering subretinal injection of LX107 injection (a gene therapy drug) to patients with retinal dystrophy caused by AIPL1 gene mutation to evaluate its efficacy and safety.",[26],"Retinal Dystrophy","RECRUITING","2026-03-09",{"date":30,"type":31},"2026-03-10","ACTUAL",{"date":33,"type":31},"2025-07-15",{"date":35,"type":20},"2030-12-31",{"name":37,"class":38},"Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":4,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":39},"100585883","functional-assessments-in-vision-impairment-100585883","NCT06908161","Functional Assessments in Vision Impairment","A Novel Approach for Capturing Real-world Functional Assessment Outcomes in Participants With a Vision Impairment","Inclusion Criteria:\n\n1. Willing to provide signed informed consent.\n2. Be available for study visits.\n3. Willing to comply with study assessments.\n4. In good general health and ambulant.\n5. Aged over 18 years of age.\n6. Have a vision impairment caused by any ocular condition which affects independent mobility.\n7. Agree to allow the research team into their home and local environments.\n8. Participate in assessments in public settings\n\nExclusion Criteria:\n\n1. Significant co-morbidities which prohibit involvement in study visits.\n2. Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.\n3. Cognitive deficiencies, including dementia or progressive neurological disease.\n4. Have a psychiatric condition that, in the investigator's opinion, precludes compliance with the protocol including past or present psychoses and bipolar disorder.\n5. Deafness or significant hearing loss.\n6. Inability to converse in English.","18 Years",{"count":49,"type":20},45,"OBSERVATIONAL","The aim of the research project is to validate the use of a novel functional assessment tool designed to document how participants with a vision impairment complete activities of daily living in a real world environment.",[53,54,55,56,26],"Retinitis Pigmentosa (RP)","Diabetic Retinopathy (DR)","Age Related Macular Degeneration (AMD)","Glaucoma","NOT_YET_RECRUITING","2025-03-26",{"date":60,"type":31},"2025-04-03",{"date":62,"type":20},"2025-04-01",{"date":64,"type":20},"2027-12-31",{"name":66,"class":38},"Center for Eye Research Australia"]