X-Linked Retinitis Pigmentosa (XLRP)

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Review clinical trials related to X-Linked Retinitis Pigmentosa (XLRP). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

InsightRP2 Registry

InsightRP2 is a secure online patient registry specific to RP2-associated retinitis pigmentosa (RP). It is our goal to further the scientific understanding of this rare disease and to support research in to a gene therapy for RP2-associated RP. We collect medical, genetic and imaging data from people affected by RP2-associated RP and will coduct a natural history study as well as image analysis studies.

Participants needed: 200
Trial details
Biological sex: AllType: ObservationalSponsor: University of GöttingenUpdated: May 21, 2025Locations: 1
Eligibility criteria

A molecular genetic diagnosis involving a heterozygous or hemizygous variant in...

Patients with evidence of non-RP2 molecular genetic diagnoses will be excluded....

Status: Recruiting

Gene Therapy for RPGR Gene Mutation-associated X-linked Retinitis Pigmentosa

The aim of this study was to evaluate the safety, tolerability, and efficacy of one-time subretinal injection of FT-002 in male subjects (8-45 years of age) with RPGR (Retinitis Pigmentosa GTPase Regulator) gene mutation-associated X-linked retinitis pigmentosa, of XLRP. This study includes Phase I (dose escalation phase) and Phase II (dose expansion phase).

Participants needed: 32
Trial details
Phase: Phase 1, Phase 2Age: 8-45Biological sex: MaleType: InterventionalSponsor: Frontera TherapeuticsUpdated: Jul 9, 2024Locations: 1
Eligibility criteria

Subjects that are willing and able to follow study procedures including schedule... [+2]

Have other retinal degenerative diseases, such as retinal degeneration caused by...