156 Participants NeededMy employer runs this trial

ASP2767 for Glaucoma

AP
Overseen ByAstellas Pharma Global Development Inc.
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: Astellas Pharma Global Development, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

Open-angle glaucoma is the most common type of glaucoma, a disease that damages the nerves in the eye and can lead to vision loss. Current treatments include eye drops, laser treatment, and surgery that help lower eye pressure. However, they do not work for everyone, and the disease may continue to worsen over time. Researchers are looking for better ways to treat open-angle glaucoma.

This is an early development study of ASP2767 in people with open-angle glaucoma. In this study, ASP2767 will be given to humans for the first time. ASP2767 is a type of treatment called gene therapy. Gene therapy uses a tool called a vector. In this study a harmless virus is used as the vector. The vector delivers genes into specific parts of the body like the eyes.

Once in the eyes these genes help nerve cells in the retina make proteins. These proteins are designed to protect the nerves in the eyes and may help slow down or prevent vision loss.

The main aims of the study are to check the safety of ASP2767 in people with open-angle glaucoma, how well they tolerate it, and to find the highest dose of ASP2767 people can safely receive. In addition, the study will also look at the effect of ASP2767 on vision in people with open-angle glaucoma.

The study has 2 phases. In both phases of the study, ASP2767 will be given as a single injection into one eye only.

In phase 1, small groups of people with open-angle glaucoma will receive ASP2767 starting with lower doses and increasing to higher doses in later groups. The people in the study will also receive prophylactic medicines which will help reduce the risk of inflammation after receiving the ASP2767 injection. Phase 1 is an open-label study. This means that people in the study and the researchers will know which treatment people are getting. Any medical problems people have at each dose level in this study will be recorded. This will help find the highest dose of ASP2767 that people can safely receive, which will also be used in phase 2.

In phase 2, another larger group of people with open-angle glaucoma will be randomly placed in 1 of 3 groups of equal size. This means each person will have an equal chance of being placed in any of the 3 groups. They will receive either the highest dose of ASP2767 that people safely received in phase 1, or a slightly lower dose of ASP2767, or a sham injection. A sham injection is a procedure that mimics the injection but does not deliver ASP2767 into the eye. To reduce the risk of inflammation due to the injection, people in the study will also receive a prophylactic medicine or placebo depending on the group they are in. The placebo will look like the prophylactic medicine and will be given in a similar way but will not have any active medicine in it. Researchers use sham injections and placebo to make sure any effect they see in people who take ASP2767 is actually caused by the drug. Phase 2 is a double-masked study, meaning neither the people in the study, nor the researchers will know who is given which treatment.

All the people in phase 1 and phase 2 will be followed up for about 1 year after receiving the treatment. After receiving their ASP2767 injection, people will visit the clinic on certain days to have health checks. They will also have their vision checked using different eye tests and will give regular blood and urine samples.

Who Is on the Research Team?

SP

Study Physician

Principal Investigator

Astellas Pharma Global Development, Inc.

Are You a Good Fit for This Trial?

This trial is for adults with open-angle glaucoma who have moderate to advanced vision loss and confirmed optic nerve damage in one eye. Participants must be able to attend regular clinic visits, complete required tests, and not join other studies during the year-long follow-up.

Inclusion Criteria

My eye pressure is 21 mmHg or lower and well controlled with my current treatment.
My vision in the study eye is at least 20/200.
I will not donate eggs during the study.
See 13 more

Exclusion Criteria

Participant has severe acute or chronic medical, psychiatric condition, physical exam finding or lab abnormality interfering with study procedures or making participant unsuitable for study
I currently have an active eye infection, not just mild blepharitis.
I have or had eye inflammation or uveitis in either eye.
See 25 more

What Are the Treatments Tested in This Trial?

Interventions

  • ASP2767

Trial Overview

The study is testing a new gene therapy called ASP2767, given as a single injection into one eye. It aims to see if ASP2767 is safe and can help protect nerves in people with glaucoma. Some participants will get different doses or a sham (fake) injection for comparison.

How Is the Trial Designed?

5

Treatment groups

Experimental Treatment

Placebo Group

Group I: Phase 2: ASP2767 Low Dose - Dose Expansion + Prophylactic RegimenExperimental Treatment3 Interventions
Group II: Phase 2: ASP2767 High Dose - Dose Expansion + Prophylactic RegimenExperimental Treatment3 Interventions
Group III: Phase 1: ASP2767 Dose Escalation + Prophylactic Regimen BExperimental Treatment2 Interventions
Group IV: Phase 1: ASP2767 Dose Escalation + Prophylactic Regimen AExperimental Treatment2 Interventions
Group V: Phase 2: Sham ASP2767 + Placebo Prophylactic RegimenPlacebo Group2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Astellas Pharma Global Development, Inc.

Lead Sponsor

Trials
204
Recruited
123,000+

Tadaaki Taniguchi

Astellas Pharma Global Development, Inc.

Chief Medical Officer

M.D., Ph.D.

Naoki Okamura profile image

Naoki Okamura

Astellas Pharma Global Development, Inc.

Chief Executive Officer

Not available