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Enrolling by invitation Phase 2 Interventional

A Study Comparing Two Doses of AGTC-501 in Male Participants With X-linked Retinitis Pigmentosa Caused by RPGR Mutations (DAWN)

ClinicalTrials.gov ID: NCT06275620

Public ClinicalTrials.gov record NCT06275620. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 10:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Open-Label Dose Escalation Study to Evaluate the Safety and Efficacy of AGTC-501 (rAAV2tYF-GRK1-RPGR) and a Phase 2 Randomized, Controlled, Masked, Multi-center Study Comparing Two Doses of AGTC-501 in Male Participants With X-linked Retinitis Pigmentosa

Study identification

NCT ID
NCT06275620
Recruitment status
Enrolling by invitation
Study type
Interventional
Phase
Phase 2
Lead sponsor
Beacon Therapeutics
Industry
Enrollment
24 participants

Conditions and interventions

Interventions

  • AGTC-501 (high dose and standard corticosteroid regimen) Biological
  • AGTC-501 (low dose and standard corticosteroid regimen) Biological
  • AGTC-501 (high dose and modified corticosteroid regimen) Biological

Biological

Eligibility (public fields only)

Age range
12 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 13, 2023
Primary completion
Oct 31, 2025
Completion
Nov 30, 2029
Last update posted
Oct 29, 2024

2023 – 2029

United States locations

U.S. sites
7
U.S. states
5
U.S. cities
7
Facility City State ZIP Site status
University of Florida Jacksonville Florida 32209
Bascom Palmer Eye Institute Miami Florida 33136
Boston Children's Hospital Boston Massachusetts 02115
Cincinnati Eye Institute Cincinnati Ohio 45242
Cleveland Clinic Cleveland Ohio 44195
Casey Eye Institute Portland Oregon 97239
Retina Foundation of the Southwest Dallas Texas 75231

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06275620, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 29, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06275620 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →