Viewing Study NCT03780257


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Study NCT ID: NCT03780257
Status: COMPLETED
Last Update Posted: 2022-04-20
First Post: 2018-12-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Study to Evaluate Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene
Sponsor: ProQR Therapeutics
Organization:

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Retinitis Pigmentosa View
None Usher Syndrome Type 2 View
None Deaf Blind View
None Retinal Disease View
None Eye Diseases View
None Eye Diseases, Hereditary View
None Eye Disorders Congenital View
None Vision Disorders View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Retinitis Pigmentosa View
None USH2A View
None RP View
None exon 13 View
None RNA therapies View
None antisense oligonucleotide View
None exon skipping View
None STELLAR View
None IVT View
None mutations in exon 13 of the USH2A gene View
None NSRP View