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NCT05902962 · ClinicalTrials.gov registry record · Phase 1

SAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects

A Phase 1 study of Retinal Dystrophy and PRPF31 Mutationassociated Retinal Dystrophy, sponsored by PYC Therapeutics.

Active
Registry status
Phase 1
Development phase
20
Enrollment target
6
Study locations

NCT05902962 is a Phase 1 study of Retinal Dystrophy and PRPF31 Mutationassociated Retinal Dystrophy that is active but no longer recruiting, run by PYC Therapeutics. The registered enrollment target is 20 participants, below the 31-participant average among 3 other Retinal Dystrophy trials with a reported enrollment target (35% lower). The trial reports 6 study locations across 4 states.

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The verdict

NCT05902962, a Phase 1 study of Retinal Dystrophy and PRPF31 Mutationassociated Retinal Dystrophy, is active but no longer recruiting, sponsored by PYC Therapeutics.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
20 participants
Enrollment target
6
Study locations

Study Summary

A Phase 1 Open-Label, Single Arm Dose Escalation Study to Evaluate the Safety and Tolerability of Intravitreally Administered VP-001 in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy

Interventions

  • DRUG VP-001

Study Locations (6)

Florida

  • University of Florida Health - Jacksonville
  • Bascom Palmer Eye Institute University of Miami - Miami

Texas

  • Retina Foundation of the Southwest - Dallas
  • Baylor College of Medicine- Alkek Eye Center - Houston

Michigan

  • University of Michigan Kellogg Eye Center - Ann Arbor

Oregon

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

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2023-04-20
Est. Completion 2025-08-30
Phase Phase 1

Sponsor

PYC Therapeutics

5 total trials

What the Registry Record Tells You About NCT05902962

The ClinicalTrials.gov registry entry for NCT05902962 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 31-participant average among 3 other Retinal Dystrophy trials with a reported enrollment target (35% lower). The listed sponsor is PYC Therapeutics, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Retinal Dystrophy appearing as the primary indexed condition, and to 1 intervention - of which VP-001 is the first listed.

NCT05902962 reports 6 study locations spanning 4 distinct geographic areas - top geographies include Florida, Texas, Michigan.

Frequently Asked Questions

What is clinical trial NCT05902962 about?

NCT05902962 is a clinical study titled "SAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects". A Phase 1 Open-Label, Single Arm Dose Escalation Study to Evaluate the Safety and Tolerability of Intravitreally Administered VP-001 in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy

What is the current status of trial NCT05902962?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2023-04-20. Estimated completion is 2025-08-30.

What conditions does trial NCT05902962 study?

This clinical trial studies the following conditions: Retinal Dystrophy, PRPF31 Mutationassociated Retinal Dystrophy, RP11.

What interventions are being tested in trial NCT05902962?

The interventions under investigation include: VP-001 (DRUG).

Who is sponsoring clinical trial NCT05902962?

This trial is sponsored by PYC Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05902962 being conducted?

This trial has 6 study locations across Florida, Michigan, Oregon, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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