Viewing Study NCT03140969

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Ignite Creation Date: 2025-12-24 @ 10:48 PM
Ignite Modification Date: 2026-01-03 @ 8:07 PM
Study NCT ID: NCT03140969
Status: COMPLETED
Last Update Posted: 2024-10-15
First Post: 2017-05-01
Is NOT Gene Therapy: True
Has Adverse Events: True
Brief Title: Study to Evaluate QR-110 in Leber's Congenital Amaurosis (LCA) Due to the c.2991+1655A>G Mutation (p.Cys998X) in the CEP290 Gene
Sponsor: Laboratoires Thea
Organization:
Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Leber's Congenital Amaurosis View
Keywords:

Keywords

Keyword Brief Keyword Text View
None CEP290 View
None p.Cys998X View
None c.2991+1655A>G View
None RNA therapy View
None Antisense oligonucleotide View
None Leber's congenital amaurosis View