EAP_GS010_single Patient

NCT03672968 | Unknown

• 1 other identifier: EAP_GS010_001
• Study Type: expanded_access
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

Expanded Access Use for a single patient of Bilateral Intravitreal Injection of GS010 in a Single Subject Affected with G11778A ND4 Leber Hereditary Optic Neuropathy

Conditions

Leber Hereditary Optic Neuropathy (Optic, Atrophy, Hereditary, Leber)

Keywords

Heredity Optic Atrophy; Leber Hereditary Optic Atrophy; Leber Hereditary Optic Neuropathy; LHON; Eye Diseases; Hereditary Eye Diseases; Inherited retinal dystrophies or degeneration; Inborn Genetic Disease; Gene Therapy; Intravitreal Injections; Mitochondrial Disease; AAV2 Vectors; Neurodegenerative Disease; Atrophy

Interventions

GS010 GENETIC

Eligibility Criteria

• Sex: all
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Presence of documented G11778A ND4 LHON-causing mutation
• Signature of informed consent and assent from the parent/guardian and the patient.

You may not qualify if:

• Contraindications to GS010 product or IVT procedures are to be checked prior to consent signature and treatment injection:
• Any known allergy or hypersensitivity to GS010 or its constituents.
• Contraindication to intravitreal injection in any eye.
• Intravitreal drug delivery to any eye within 30 days prior to the injection
• Previous vitrectomy in either eye.
• Narrow angle in any eye contra-indicating pupillary dilation.
• Presence of disorders or diseases of the eye or adnexa, excluding LHON, which may interfere with visual or ocular assessments, including SD-OCT, during the study period.
• Presence of known/documented mutations, other than the G11778A ND4 LHON-causing mutation, which are known to cause pathology of the optic nerve, retina or afferent visual system.
• Presence of systemic or ocular/vision diseases, disorders or pathologies, other than LHON, known to cause or be associated with vision loss, or whose associated treatment(s) or therapy(ies) is/are known to cause or be associated with vision loss.
• Presence of optic neuropathy from any cause except LHON.
• Presence of illness or disease that, in the opinion of the Investigator, include symptoms and/or the associated treatments that can alter visual function, for instance cancers or pathology of the central nervous system, including Multiple Sclerosis (diagnosis of Multiple Sclerosis must be based on the 2010 Revisions to the McDonald Criteria \[Polman 2011\]).
• History of recurrent uveitis (idiopathic or immune-related) or active ocular inflammation.
• Previous treatment with ocular gene therapy in either eye.
• Subjects who have undergone ocular surgery of clinical relevance (per Investigator assessment) within 90 days prior to injection.
• Subjects who are unable to tolerate (e.g. the immune modulating regimen) or unable or unwilling to comply with all the protocol requirements.

Sponsors & Collaborators

• GenSight Biologics: lead

Related Links

• Related Info

MeSH Terms

Conditions

Optic Atrophy, Hereditary, Leber; Atrophy; Eye Diseases; Eye Diseases, Hereditary; Genetic Diseases, Inborn; Mitochondrial Diseases; Neurodegenerative Diseases

Condition Hierarchy (Ancestors)

Optic Atrophies, Hereditary; Optic Atrophy; Optic Nerve Diseases; Cranial Nerve Diseases; Nervous System Diseases; Heredodegenerative Disorders, Nervous System; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Metabolic Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Anatomical; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: expanded access
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 13, 2018
• First Posted: September 17, 2018
• Last Updated: March 2, 2026

Record last verified: 2026-02