Last reviewed · How we verify

NCT05573984

Natural History of PRPF31 Mutation-Associated Retinal Dystrophy

Active, enrolled Last updated 13 April 2026
What this trial tests

trial in Retinitis Pigmentosa in 50 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
7 July 2022
Primary endpoint
9 September 2026
1 November 2026

Quick facts

Lead sponsorPYC Therapeutics
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment50
Start date7 July 2022
Primary completion9 September 2026
Estimated completion1 November 2026
Sites7 locations across United States, Australia

Conditions studied

Sponsor

PYC Therapeutics — full company profile →

Who can join

10 and older, any sex, with Retinitis Pigmentosa or Eye Diseases, Hereditary. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Retinitis Pigmentosa

Currently open trials in the same condition.

Other PYC Therapeutics trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05573984.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing