Under construction – not a live service
Sign in
Taking people in ChinaEarly phase 1

Gene Therapy Tested in People With X-linked Retinitis Pigmentosa

Tests FT-002, a gene therapy injected into the eye, in people with X-linked retinitis pigmentosa.

Plain-language title generated from the registry record
Registry title: Gene Therapy for Subjects With RPGR Mutation-associated X-linked Retinitis Pigmentosa

Key facts

Where
Beijing and Shanghai, ChinaSee the 2 sites
Phase
Early phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 8 and 45 years old?

Source: NCT05874310, who can take part

Where in China

  • Peking Union Medical College HospitalBeijing, ChinaTaking people
  • Eye ENT Hospital of Fudan UniversityShanghai, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Frontera Therapeutics
Trial code
NCT05874310
Record updated
24 May 2023
Original description
A clinical trial of gene therapy for patients with X-linked retinitis pigmentosa (XLRP).Read full original descriptionShow less

An Open-label, Single-center, Dose-escalation Clinical Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Intraocular Administration of FT-002 in Subjects With RPGR Mutation-associated X-linked Retinitis Pigmentosa.

A clinical trial of gene therapy for patients with X-linked retinitis pigmentosa (XLRP).

Inclusion: 1.Subjects that are willing and able to follow study procedures; 2.Males aged 8-45 years old at the time of signing the Informed Consent Form; 4.Subjects who are confirmed with variants of RPGR .

Exclusion: 1.Have other retinal degenerative diseases, such as retinal degeneration caused by other known Inherited retinal disease gene variants or previously received an gene therapy product.

ClinicalTrials.gov NCT05874310