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ACTIVE NOT RECRUITING

Natural History of PRPF31 Mutation-Associated Retinal Dystrophy

NCT05573984 · View on ClinicalTrials.gov ↗

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.

Study Locations (7)

California

  • University of California San Francisco — San Francisco

Florida

  • University of Florida Health — Jacksonville

Michigan

  • University of Michigan Kellogg Eye Center — Ann Arbor

Oregon

  • Oregon Health and Science University - Casey Eye Institute — Portland

Texas

  • Retina Foundation of the Southwest — Dallas

Western Australia

  • Lions Eye Institute — Nedlands

Other

  • Centre For Eye Research Australia (CERA) - Retinal Gene Therapy Unit — East Melbourne

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-07-07
Est. Completion 2026-02-28

Sponsor

PYC Therapeutics

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05573984

The ClinicalTrials.gov registry entry for NCT05573984 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is PYC Therapeutics, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Retinitis Pigmentosa appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05573984 reports 7 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Michigan. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05573984 about?

NCT05573984 is a clinical study titled "Natural History of PRPF31 Mutation-Associated Retinal Dystrophy". 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 fun...

What is the current status of trial NCT05573984?

This trial is currently active not recruiting. The enrollment target is 50 participants. The study started on 2022-07-07. Estimated completion is 2026-02-28.

What conditions does trial NCT05573984 study?

This clinical trial studies the following conditions: Retinitis Pigmentosa, Retinal Dystrophies, Eye Diseases, Hereditary, Retinal Dystrophy Rod, Retinal Dystrophy Rod Progressive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT05573984?

This trial is sponsored by PYC Therapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05573984 being conducted?

This trial has 7 study locations across California, Florida, Michigan, Oregon, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial