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Clinical Trials in the USA / NCT05573984
Active, not recruiting Observational

Natural History of PRPF31 Mutation-Associated Retinal Dystrophy

NCT05573984 · tracked via the Priya Life Science USA tracker
Sponsor
PYC Therapeutics
Phase
Observational
Started
2022-07-07
Last updated
2026-04-13

Condition(s) studied

Retinitis PigmentosaEye Diseases, HereditaryRetinal DystrophiesRetinal Dystrophy RodRetinal Dystrophy Rod Progressive

Study summary

The purpose of this study is to characterize the natural history through temporal systemic evaluation of subjects identified with PRPF31 mutation-associated retinal dystrophy, also called retinitis pigmentosa type 11, or RP11.

Assessments will be completed to measure and evaluate structural and functional visual changes including those impacting patient quality of life associated with this inherited retinal condition and observing how these changes evolve over time.

Eligibility

Sex
ALL
Min age
10 Years
Max age
Healthy volunteers
No
Inclusion Criteria: Participants must meet all of the following in order to be enrolled into the study: 1. Male or female, ≥ 10 years of age at baseline (Visit 2). 2. Have a clinical and molecular diagnosis of PRPF31 mutation-associated retinal dystrophy. 3. If ≥ 18 years of age, understand the language of the informed consent and are willing and able to provide written informed consent prior to any study procedures. If \< 18 years of age, are willing to assent to study participation in writing and have a legally authorized representative provide written informed consent on your behalf. 4. Are willing to comply with the instructions and attend all scheduled study visits. Exclusion Criteria: Participants or, in the case of ocular-specific criteria, individual eyes with any of the following will not be allowed to participate in this study: 1. Have any uncontrolled systemic disease that, in the opinion of the Investigator, would preclude participation in the study (e.g., infection, uncontrolled elevated blood pressure, cardiovascular disease, or glycemic control issues) or put the participant at risk due to study procedures. 2. Have mutations in genes that cause autosomal dominant retinitis pigmentosa (adRP), X-linked retinitis pigmentosa (XLRP), or presence of biallelic mutations in autosomal recessive RP/retinal dystrophy genes other than PRPF31 mutations. 3. Have used anti-vascular endothelial growth factor (VEGF) agents or corticosteroid injections or implants. 4. Have had Ozurdex® implants placed within 3 months or Retisert® or Iluvien® implants placed within 3 years prior to Visit 2. 5. Within 3 months prior to Visit 2, have undergone any vitreoretinal surgery (scleral buckle, pars plana vitrectomy, retrieval of a dropped nucleus or intraocular lens, radial optic neurotomy, sheathotomy, cyclodestructive procedures or multiple filtration surgeries \[2 or more\], etc.) or any other ocular surgery. 6. Have ocular media opacity or poor pupillary dilation that prohibits quality ophthalmic evaluation or photography. 7. Have used any investigational drug or device within 90 days or 5 estimated half-lives of Visit 2, whichever is longer, or plan to participate in another study of drug or device during the study period. 8. Have received any prior cell or gene therapy for a retinal condition. 9. Have a history of illicit drug use or alcohol dependency.

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
University of California San Francisco San Francisco California
University of Florida Health Jacksonville Florida
University of Michigan Kellogg Eye Center Ann Arbor Michigan
Oregon Health and Science University - Casey Eye Institute Portland Oregon
Retina Foundation of the Southwest Dallas Texas
Lions Eye Institute Nedlands Western Australia
Centre For Eye Research Australia (CERA) - Retinal Gene Therapy Unit East Melbourne Australia

More PYC Therapeutics trials in the USA

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05573984 on ClinicalTrials.gov ↗ ← All trials in the USA