Laruparetigene Zovaparvovec for Retinitis Pigmentosa
(Landscape Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment, laruparetigene zovaparvovec, to determine if it can safely help individuals with X-linked Retinitis Pigmentosa (XLRP) preserve or improve vision. The treatment is administered through a procedure in both eyes. Suitable candidates for this trial are males diagnosed with XLRP who can undergo eye surgery. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to significant advancements in vision care.
Do I need to stop taking my current medications for the trial?
The trial requires that you stop taking anticoagulant agents (like warfarin or heparin) 7 days before the study drug is given. You also need to stop using systemic corticosteroids or other immunosuppressive medications 3 months before the study drug is given. If you have a history of herpes, you must be willing to use antiviral medication.
Is there any evidence suggesting that laruparetigene zovaparvovec is likely to be safe for humans?
Research has shown that laruparetigene zovaparvovec, also known as AGTC-501, has generally been well-tolerated. In one study, participants handled the treatment well for up to 36 months. Another study found positive results at 9 months, with no major safety issues. These findings suggest the treatment is relatively safe. However, individual experiences can differ, so discussing any concerns with the trial team is important.12345
Why do researchers think this study treatment might be promising?
Unlike the standard treatments for retinitis pigmentosa, which often focus on managing symptoms or slowing progression, laruparetigene zovaparvovec offers a novel gene therapy approach. This treatment is unique because it involves delivering a modified gene directly to the retinal cells through a subretinal injection, potentially addressing the root genetic cause of the disease. Researchers are excited about laruparetigene zovaparvovec because it has the potential to restore vision at a cellular level, offering hope for significant improvement rather than just symptom management.
What evidence suggests that laruparetigene zovaparvovec might be an effective treatment for retinitis pigmentosa?
Research has shown that laruparetigene zovaparvovec, also known as AGTC-501, may improve vision for people with X-linked retinitis pigmentosa (XLRP). Studies have found early improvements in seeing in low-light conditions and lasting benefits in overall eye sensitivity. Data from participants indicated positive changes in vision over several months, suggesting that the treatment might slow down or even improve vision loss. Most participants tolerated the therapy well, experiencing only minor side effects. These findings offer hope that laruparetigene zovaparvovec could effectively manage XLRP.12367
Who Is on the Research Team?
None None
Principal Investigator
Are You a Good Fit for This Trial?
This trial is for male participants with X-Linked Retinitis Pigmentosa, a genetic eye condition that leads to vision loss. Details about who can join or reasons for exclusion are not provided, so interested individuals should contact the study organizers for full eligibility criteria.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo pars plana vitrectomy and receive a central subretinal administration of laruparetigene zovaparvovec in both eyes
Follow-up
Participants are monitored for safety and effectiveness after treatment
Long-term follow-up
Participants are monitored for long-term safety and effectiveness
What Are the Treatments Tested in This Trial?
Interventions
- Laruparetigene Zovaparvovec
Find a Clinic Near You
Who Is Running the Clinical Trial?
Beacon Therapeutics
Lead Sponsor